Xiaoxiao Du
Sheng Chang2
Wenzhi Guo
Shuijun Zhang- 1Henan Key Laboratory of Digestive Organ Transplantation, Open and Key Laboratory of Hepatobiliary & Pancreatic Surgery and Digestive Organ Transplantation at Henan Universities, ZhengZhou Key Laboratory of Hepatobiliary & Pancreatic Diseases and Organ Transplantation, Department of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China
- 2Key Laboratory of Organ Transplantation, Institute of Organ Transplantation, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Ministry of Education, NHC Key Laboratory of Organ Transplantation, Key Laboratory of Organ Transplantation, Chinese Academy of Medical Sciences, Wuhan, China
Liver transplantation is currently the most effective method for treating end-stage liver disease. However, recipients still need long-term immunosuppressive drug treatment to control allogeneic immune rejection, which may cause various complications and affect the long-term survival of the recipient. Many liver transplant researchers constantly pursue the induction of immune tolerance in liver transplant recipients, immunosuppression withdrawal, and the maintenance of good and stable graft function. Although allogeneic liver transplantation is more tolerated than transplantation of other solid organs, and it shows a certain incidence of spontaneous tolerance, there is still great risk for general recipients. With the gradual progress in our understanding of immune regulatory mechanisms, a variety of immune regulatory cells have been discovered, and good results have been obtained in rodent and non-human primate transplant models. As immune cell therapies can induce long-term stable tolerance, they provide a good prospect for the induction of tolerance in clinical liver transplantation. At present, many transplant centers have carried out tolerance-inducing clinical trials in liver transplant recipients, and some have achieved gratifying results. This article will review the current status of liver transplant tolerance and the research progress of different cellular immunotherapies to induce this tolerance, which can provide more support for future clinical applications.
Introduction
Liver transplantation has been a preferred option for patients with end-stage liver disease. Since Dr. Starzl performed the first human liver transplantation in 1963, the short-term survival rate of liver transplant recipients has improved significantly, which can be attributed to advances in surgical techniques and immunosuppression (IS) agents (1). However, owing to the long-term use of IS agents, complications concerning the cardiovascular and cerebrovascular systems, diabetes, chronic renal insufficiency, infection, or tumors seriously affect the long-term survival of liver transplant recipients (2, 3).
Immunological self-tolerance refers to the ability of a healthy immune system to produce a protective immune response to pathogens and foreign antigens while maintaining tolerance to its own tissues. Therefore, transplant tolerance refers to accepting organs without the need for long-term IS and maintaining protective immunity (4). Tolerance is usually classified as complete immune tolerance, operational tolerance (OT), and prope tolerance, referred to a condition with a low, non-toxic dose of IS (5). In clinical applications, the focus of the study is OT, that is, long-term functional graft survival in a patient not requiring maintenance IS (6).
The liver is an immunologically privileged organ compared to other transplant organs such as the heart, kidney, or pancreas (7). Liver transplant recipients generally maintain a low level of IS and the hepatic graft can provide immunological protection when transplanted in combination with other solid organs (8). Since Calne first recognized the liver tolerance effect (8) in 1969, people have been enthusiastic about the induction of liver immune tolerance.
As the body's largest digestive organ, the liver has two sets of blood supplies, the portal vein and the hepatic artery. It is constantly exposed to enterically-derived blood-borne pathogens, which gives the liver a unique form of immune privilege (9). Numerous sinuses constitute the largest reticuloendothelial system in the human body and contain the largest number of specialized and non-specialized antigen-presenting cells (APC) and cells that maintain liver immune tolerance, including resident macrophages (also known as Kupffer cells), dendritic cells, hepatocytes, hepatic sinusoidal endothelial cells (LSECs), and hepatic stellate cells (HSCs) (10). When pathogen-derived products such as lipopolysaccharides pass through the liver, like an immune filter, their concentration could be reduced 100-fold, enabling the hepatic immune microenvironment to have sufficient capacity to regulate the nature and intensity of its response (11). Numerous immune regulatory mechanisms in the liver, including downregulation of co-stimulatory molecules, secretion of inhibitory cytokines, inhibition of effector T cell activation, and induction of regulatory T cells, predispose the immune response of the liver to tolerance rather than activation (12).
Current State in Spontaneous Tolerance
Factually, in liver transplantation, spontaneous tolerance initially came from the casual clinical observation. Owing to poor compliance, infection complications, posttransplant lymphoproliferative disease (PTLD) or doctor's advice, some liver transplant recipients developed spontaneous tolerance after discontinuing IS, which has aroused great interest of transplant researchers. In 1993, Reyes et al. in Pittsburgh reported that 8 liver transplant recipients with poor compliance ceased IS from 0.5 to 11 years after transplantation, but unexpectedly developed OT. Among them, after weaving from IS, 7 recipients maintained good allograft function for 1 to 14.3 years. The remaining recipient underwent liver retransplantation after 7.7 years of IS withdrawal for viral hepatitis. In addition, 6 recipients were shown to have systemic chimerism (13).
Over nearly three decades, many liver transplant centers have conducted clinical trials of IS withdrawal in both adult and pediatric liver transplant recipients. It has been reported that normal liver function was successfully maintained in adult and child liver transplant recipients, with ~20% of patients (6–63%) achieving complete immunosuppressive withdrawal (Tables 1, 2) (14–33).
Table 1. Immunosuppression withdrawal trials (≥10 recipients, single center).
Table 2. Immunosuppression withdrawal trials (≥10 recipients, Mul-Center).
Sanchez-Fueyo et al. of the Hospital Clinic of Barcelona conducted a prospective and multicenter IS withdrawal clinical trial in 98 liver transplant recipients (NCT00647283). Of these, 41 achieved clinical tolerance (41.8%) and 57 developed mild rejection (58.2%), which was followed by remission within 5.6 months. During the 3-year follow-up after IS withdrawal, no significant histological damage was found in liver biopsies of the tolerant recipients. Statistical analysis showed that years post-transplantation correlated positively with tolerance induction and could be the strongest predictor (27).
Comparing with calcineurin inhibitors (CNI), sirolimus, a kind of rapamycin inhibitor (mTOR-I), has no significant drug toxicity, such as nephrotoxicity, hypertension, diabetes, infections and neoplasms (34). Another advantage of sirolimus is its immunomodulatory ability that could facilitate safe IS withdrawal (35). To assess if sirolimus could increase the tolerability in liver transplant recipients, Levitsky et al., at Northwestern University, performed a prospective clinical trial of single sirolimus withdrawal (NCT02062944). They recruited 15 recipients with non-viral or immunological hepatitis more than 3 years after liver transplantation. After 12 months from sirolimus withdraw, it showed that 8 recipients (53%) achieved OT. Of the other 7 patients, 3 failed IS withdrawal, 3 developed moderate cellular rejection (TCMR) on liver biopsies at the end of the study, and 1 was withdrawn from the trial owing to adrenal metastasis of hepatocellular carcinoma (32). The current result showed the OT rate of sirolimus was comparable to CNI-withdrawal studies. Except for free CNI toxicity, whether liver recipients can benefit more from sirolimus withdrawal, it still needs more and larger trials.
For pediatric liver transplant recipients, Feng et al. in the University of California conducted a multicenter, prospective clinical trial of IS withdrawal (WISP-R, NCT00320606). A total of 12 (60%) of the 20 enrolled pediatric recipients achieved clinical tolerance, and during follow-up for more than 2 years after IS withdrawal, the graft function was normal and there was no significant change in biopsy compared with baseline. A total of 3 recipients underwent acute rejection (n = 2) or uncertain rejection (n = 1) during IS withdrawal, and 4 recipients failed to achieve clinical tolerance owing to uncertain acute rejection within 1 year of drug withdrawal. Their graft function recovered to normal after increased or restarted IS. Another recipient was withdrawn from the study after IS withdrawal for violating exclusion criteria. Similar to the results of the adult study, the time after transplantation was significantly longer in the tolerance group than in the non-tolerance group, suggesting that the time after transplantation is an important predictor of tolerance formation (26). Of 12 OT recipients followed for 5 years, 9 cases were positive for class I or class II DSA, but no cases resulted in chronic rejection, graft loss, or death. According to the graft biopsy, there was no progressive increase in inflammation or fibrosis, suggesting that liver grafts after immune retreat can maintain stability during a certain period of time (30).
There are also many studies focused on biomarkers that can predict immune tolerance. Bohne, et al. found that recipients with spontaneous tolerance show an increased number of natural killer (NK) cells and γδT cells in peripheral blood. High levels of hepcidin in liver tissues and ferritin in the serum, increased iron deposits in hepatocytes, and high expression of the related liver tissue genes can accurately predict the outcome for a group of independent patients with IS withdrawal (36). Mazariegos et al. showed that the ratio of monocytoid dendritic cells (mDC) and plasmacytoid dendritic cells (pDC) precursors in the peripheral blood of patients with tolerance increased significantly compared to the healthy control group and the IS maintenance group (37). Levitsky et al. also found that, compared with the baseline, the tolerogenic dendritic cells (tolDC), regulatory B cells (Breg), and cell phenotypes associated with chronic antigen presentation in peripheral blood of the OT group was significantly higher than that of the non-OT group. In addition, gene signatures in peripheral blood/biopsy tissue showed that 12/14 LTR could accurately predict tolerance (32). Chruscinski et al. performed a clinical trial (NCT02541916) for the predictive value of gene signatures in peripheral blood/biopsy tissue. Preliminary results suggest that 5 of the 9 patients, consistent with the inclusion criteria, had discontinued IS for more than 2 years (38). However, the feasibility of this method still needs to be verified by adequate prospective, multicenter, large-scale follow-up trials.
Long-term studies on the safety of immunosuppressive IS withdrawal regimens are inconclusive, and most of them lack evidence of invasive liver biopsy. However, direct comparisons of these trials are difficult because of the lack of standardization. According to the current research results, the acute rejection rate after IS withdrawal varies from 12 to 76% (Tables 1, 2), but it is generally moderate and almost reversible. Chronic rejection is rare (0–6%), and the incidence of graft loss owing to rejection is extremely low (39, 40). Over time, however, the prevalence and severity of chronic graft injury such as subclinical rejection, chronic portal inflammation, borderline hepatitis, and/or fibrosis (periportal and/or perivenous) would increase (41–51). Ten years after transplantation, most studies report that normal histology is present in up to 30% of allografts; bridging fibrosis and/or cirrhosis may be equally common, accounting for about 60% (42, 45, 52). The transcriptome analysis of liver tissue revealed an expression profile very similar to that of T-cell mediated rejection (53). Notably, more than 90 percent of patients who stopped IS 20 years after the transplant did not experience rejection (27). To date, there is no definitive data suggesting that progressively abnormal histology leads to loss of liver graft or death of recipient. However, the OT is not a permanent stable state, still needed regular inspection and to deal with in time.
Because of the difficulty to conduct prospective, multicenter, and longitudinal long-term studies on clinical transplant tolerance, the risk of IS withdrawal in liver transplant recipients remains uncertain. However, based upon a broad understanding of liver disease, increased fibrosis in the allograft indicates the development of portal hypertension and associated complications. IS withdrawal alone could make recipients at the risk of re-transplantation after some years, especially for pediatric recipients. Therefore, there is a wide area of research for the development of induced liver tolerance, especially with cell therapies.
Hematopoietic Stem Cell Transplantation (HSCT) for the Induction of Liver Transplantation Tolerance
Mixed hematopoietic chimerism is associated with alloantigen tolerance, a phenomenon first identified by Owen in freemartin cattle (fraternal twins sharing placental circulation retain allogeneic tolerance to each other after birth) in 1945 (54). Subsequently, Kashiwagi and Starzl discovered donor immunoglobulin in the peripheral blood of liver recipients in 1969, proposing the concept of chimerism in human transplantation (55).
In a series of pioneering studies that began in 1961, Till and McCulloch demonstrated that bone marrow consists of a group of cells, known as hematopoietic stem cells (HSCs), which have the ability to self-renew and differentiate into multiple myeloid cell types (56–58). Afterward, Starzl et al. observed persistent multilineage hematopoietic microchimera (defined as <1% donor cells) in both lymphoid and non-lymphoid tissues of long-lived liver or kidney transplant recipients, including patients on IS for many years after transplantation in 1993 (59). Over the past 30 years, many researchers have been exploring ways to induce tolerance of solid organ transplantation (SOT) using HSCT. Both autologous and allogeneic HSCT have been applied to induce transplant tolerance clinically (60–63).
Clinically, hematopoietic stem cells were first harvested from the bone marrow of the ilium (64). In the 1990s, the protocol to mobilize stem cells into peripheral circulation with granulocyte colony-stimulating factor (G-CSF) and isolate from PBMC by magnetic activated cell sorting (MACS) or flow sorting, thereby separating CD34+ cells, greatly amplified the clinical application of HSCT. Subsequent studies show that combination with chemokine receptor 4 antagonist (AMD3100) and G-CSF can mobilize stem cells more effectively (65).
Allogeneic HSCT Inducing Chimerism
After lymphoablation of the recipient, transfusion of allogeneic donor bone marrow can lead to mixed hematopoietic chimerism, where genetically different donor HSCs are implanted into the host and differentiate into donor-derived lymphocytes that coexist with the host. Central tolerance is a key mechanism of allograft tolerance induced by long-term HSCs (66). When donor bone marrow is injected into the host that has undergone lymphoablation, such as total lymphoid irradiation (TLI) and anti-thymocyte globulin (ATG), HSCs are implanted into the recipient bone marrow and thymus for differentiation, and the host immune system is repopulated with various lymphocyte cells from the donor following by the immunoreconstitution. The presence of donor progenitor cells in the thymus leads to the apoptosis of T cells that recognize the donor antigen expressed by the transplanted organ itself without developing and donor-reactive T cells would undergo clonal deletion, so the host can tolerate the allograft (67). The coexistence of host and donor hematopoietic cells is called chimera, and it is this chimera state in the host that drives central tolerance. According to the percentage of hematopoietic cells of donor origin, the chimerism was divided into microchimerism (donor <1%) and two forms of macrochimerism: full chimerism (donor ~100%) and mixed chimerism (donor >1% but <100%) (68). Although central tolerance is the primary mechanism for HSCs-induced tolerance to homo-antigens, it may be incomplete, in part because not all donor antigens are expressed by HSCs in the host thymus. Furthermore, T lymphocytes with low affinity for their own antigens may escape the selection process, thereby entering the peripheral lymphocyte cycle. In fact, peripheral mechanisms are needed to maintain immune tolerance when the self-reactive T cell subsets evade the thymus selection process. In the transplant environment, a mild pre-treatment regimen designed to induce chimerism can also control the survival of mature alloreactive T cells through peripheral regulation mechanisms, resulting in clone deletion, anergy, or apoptosis of the extra-thymic alloreactive T lymphocytes (66, 67, 69–71). Persistent microchimerism may also be an important determinant for long-term graft survival and transplant tolerance (72, 73).
Since the mid-twentieth century, scientists have used HSC transfusion by injecting donor bone marrow to alter host immune responses in a variety of autoimmunity diseases and solid organ transplantation (SOT) (74, 75). The ideal state of clinical transplant tolerance is to combine HSCT with SOT from the same donor to form a stable hematopoietic chimera of donor and recipient (76). However, myeloablative therapy carries significant risks, most notably graft vs. host disease (GVHD) and severe infections, which are too high-risk to be applied in liver transplants routinely. Therefore, researchers investigated protocols for non-myeloablative bone marrow transplant, including co-stimulatory molecules blockade, low dose irradiation, T cell depletion by monoclonal antibody, etc. (77–79). Chimerism has always been the main method of inducing tolerance in renal transplantation. Clinical studies on transplant tolerance induced by bone marrow chimerism in renal allografts have also achieved gratifying results. In 2008, Kawai et al. reported the first successful application of mixed chimerism tolerance in human kidney transplantation without long-term maintenance of IS (80). The authors then reported that 5 out of 10 kidney recipients had achieved transplant tolerance. Although the detectable duration of chimerism was transient, it was observed that donor-specific mixed lymphocyte response (MLR) and CTL activity decreased in vitro and FOXP3 mRNA level increased in vivo (81). Based on the enriching of HSC with tolerogenic CD8+/TCR− facilitating cells (FC) and the depleting of GVHD-producing cells, Leventhal et al. performed a clinical trial in 19 patients with uremia undergoing combined HLA-mismatched hematopoietic stem cell/kidney transplantation. Then 12 of them achieved stable chimerism and OT status of 8–48 months without GVHD after IS withdraw (82). Scandling et al. reported that 16 of 22 HLA-matched patients who had received the same treatment regimen established a persistent mixed chimera (>12 months), with successful withdrawal from immunosuppressants. Renal graft function was stable for up to 7 years after withdrawal, and no incidence of GVHD or rejection was observed (83).
In the field of liver transplantation, there have been some case reports and clinical trials with HSCT transfusion. Ringden et al. reported a liver cancer patient who received HSCT from the same donor after liver transplantation, underwent preoperative myeloablation, achieved chimerism, but subsequently died of opportunistic infection (84). Donckier et al. recruited 5 patients with advanced hepatocellular carcinoma (HCC) who underwent living liver transplantation and received donor CD34+ stem cell transfusion based on the induction regimen of non-myeloablative therapy. Two patients successfully stopped IS without allograft rejection. Three patients developed acute cellular rejection after immunosuppressant withdrawal, two of which were given steroid pulse therapy, whereas the other was reintroduced to calcineurin inhibitor (CNI) immunosuppressive therapy, with no observation of macrochimerism (85, 86). Tryphonopoulos et al. recruited 45 adults who received cadaver livers and subsequently underwent transfusion of donor bone marrow cells on the day of the transplant. IS were discontinued for more than 3 years, starting 3 years after surgery. Acute rejection occurred in 69% of the treated patients, and immunosuppressive therapy was successfully withdrawn in 22.2% of the treated recipients. However, there was no significant increase in the success of withdrawal and chimerism levels, compared to patients who did not receive bone marrow transplants (20). Liver transplantation is mainly performed from cadaver donors, and recipients generally suffer from severe diseases during the perioperative period, as well as postoperative coagulation and circulatory dysfunction, which may lead to serious infection and tumor recurrence.
Surprisingly, Alexander et al. reported a successful case that a 9-year-old girl with type O, RhD negative underwent RhD blood type conversion to positive after receiving the liver graft of a male donor with type O, RhD positive. Furthermore, CD19 + B cells (XY) were found in the sample of bone marrow puncture. Peripheral blood lymphocyte analysis showed that 94% of T cells came from male and 6% from female; 98% of the B cells came from male and 2% from female; 100% of the granulocytes and NK cells came from male. These results support the formation of chimera. When IS was withdrawn 14 months after transplantation, both the graft and the recipient were healthy for 5 years without GVHD or acute rejection. This indicates that fully tolerated chimera can still occur under certain conditions (87).
For the application of allogeneic HSCT in liver transplant tolerance and chimerism, there are some challenges to overcome, e.g., the risk of serious infection, coagulation and circulatory dysfunction following the myeloablative, the tumor recurrence and the permanence of existence in recipient.
Autologous HSCT Inducing Chimerism
Autologous HSCT is performed by pre-collecting and cryo-preserving autologous bone marrow or peripheral blood stem cells isolated from the patient and then re-transfusing after myeloablative treatment to reconstruct the immune system, which could lead to a more tolerant immune system (88, 89). In autologous stem cell transplantation, the cells come from the recipient, which theoretically prevents the possibility of immune rejection or GVHD. Moreover, autologous bone marrow or peripheral stem cells are easier to obtain and store.
Although there are some differences between allogeneic and autologous HSCT with regard to tolerance mechanisms, they both attempt to reconstruct the recipient immune system and achieve immune tolerance through “re-education.” The basic principle of autologous HSCT is to first eliminate reactive and memory immunity and then regenerate the immune system; that is, to exhaust autoreactive and memory T and B cells through a myeloablative or non-myeloablative regimen, followed by reconstruction of immune tolerance (89, 90). The immune monitoring analyses have shown that this can recreate new auto-tolerant immune T and B cell banks, enhance immune regulation mechanisms, and induce changes in the recipient's anti-inflammatory environment (63, 91–95). Muraro et al. found a large number of new T cell clones emerged after autologous HSCT in patients with multiple sclerosis (MS), substituting for the original T cell receptor (TCR) bank and showing a greater diversity of TCR spectrum (63). The immune cell gene expression profiles showed that the number of CD3 + cells remained low after autologous HSCT, and the number of CD8 + cells could return to normal after 3 months postoperatively (92). Another important phenotypic observation is that the recipient's CD4 + CD25 + FoxP3 + regulatory T cells (Tregs) were significantly increased (96–98) and so were the CD8 + Foxp3 + Tregs (99), compared to the preoperative state. The ratio of Bregs increased briefly after autologous HSCT and remained at a higher level for at least 2 years after transplantation, suggesting that Bregs may be involved in the reconstruction of self-tolerance after AHSCT (95, 100). In addition, a variety of cells, such as IL-2, IL-4, IL-6, IL-8, IL-10, IL-17, IL-18, IFN-γ, TNF-α, and TGF-β play an essential role in immune reconstruction and regulation (95, 97).
In recent years, autologous HSCT has been used in clinical trials to eliminate various types of refractory autoimmune diseases such as multiple sclerosis, systemic sclerosis (SSc), systemic lupus erythematous (SLE), rheumatoid arthritis (RA), Crohn's disease, juvenile arthritis, and type 1 diabetes (T1D), presenting better results than traditional therapies and showing promising prospects for long-term remission of autoimmune diseases without IS (90, 93, 95, 101–105). At present, autologous HSCT has also been widely used in various types of liver cirrhosis, improving liver function in varying degrees (106–109). Coupled with the study of transplant animal models, these studies provide abundant theoretical basis for expanding autologous HSCT application in organ transplantation (110–112).
In Toronto University (Canada), Levy et al. have performed a clinical trial on autologous HSCT for allogeneic organ transplant tolerance (ASCOTT) (NCT02549586) (38). Six liver transplant recipients were recruited, five of whom were enrolled. The HSCs of patients were mobilized, purified, and cryopreserved ahead of liver transplant. After immune ablation (Busulfan + Cyclophosphamide + rabbit anti-thymocyte globulin), the patients received autologous HSCT and liver transplantation. IS was withdrawn in five patients with evidence of deletion of alloreactive T cell clones. Two of them were still healthy at 406 and 518 days after HSCT; one died of heart failure at 212 days, one patient received re-transplantation at 166 days after HSCT owing to complications of venous occlusive disease, and one patient died of erythrocytic syndrome at 87 days after HSCT. However, non-hematological toxicity in grades 3–4 was found in almost all patients. It is suggested that there is a certain application prospect of HSCT-induced immune tolerance after liver transplantation, but the potential toxicity is an important problem to be solved.
CD4 + Regulatory T Cells in Liver Transplant Tolerance
Under physiological conditions, Tregs account for 5–10% of CD4 + T cells in peripheral blood. Tregs are characterized by high stable expression of CD25 and FoxP3, and are divided into natural regulatory T cells (nTreg) produced in the thymus and peripherally induced regulatory T cells (iTreg) (113). Modern research shows that CD4 + Treg is the key to control self-tolerance. The combination can induce peripheral tolerance to autoantigens and alloantigens through a variety of mechanisms, mainly cell-to-cell contact-induced cell lysis, local depletion of IL-2, inhibition of DC maturity, downregulation of DC function, secretion of immunosuppressive cytokines (such as IL-10, IL-35, and TGF-β), etc. (114). In addition, Tregs can migrate to the inflammation site, and their inhibitory activity is usually located in the inflammation site, without significant effects on overall immunity (115).
In rodent models of liver transplantation tolerance, Tregs are present in increased proportion in liver grafts and are involved in the induction of liver tolerance (116, 117). Relevant clinical studies have also shown that, in OT liver transplantation recipients, the proportion of Tregs in peripheral blood and liver increases, which shows a protective effect on liver allografts (118, 119). Therefore, the use of Tregs to mediate transplant tolerance is an important part of transplant immunology research.
Treg adoptive infusion is a method to induce tolerance, where the principle is to tilt the immune response toward Treg dominance, rather than to cause rejection of T effector cells, in order to reduce the dependence of patients receiving solid organ transplantation on immunosuppressant drugs.
It is now generally accepted that the best method to make Treg clinically is to effectively expand it in vitro and maintain high purity and inhibitory activity (115). Under certain culture conditions, human Treg can be expanded to 100–1,000 times in 2 weeks (120, 121). The required cell dose varies depending on the type of disease and the presence or absence of combination therapy (115, 122, 123). Treg separation and purification methods mainly include MACS and flow cytometry sorting.
Some researchers have used the chimeric antigen receptor (CAR) technology to produce donor antigen-specific Treg (CAR-Treg) and can overcome the limitation of alloantigen-stimulation-based protocols in vitro. In these studies, CARs could be developed to redirect Tregs toward a specific donor leucocyte antigen (HLA) class I molecule (HLA-A2). Unlike HLA class II, the selected donor HLA class I is expressed ubiquitously in grafts. Compared with polyclonal Tregs, CAR-Treg could have better safety, stability, and effectiveness in theory and have strong therapeutic potential to protect allograft (124–127).
Clinical trials of various autoimmune diseases and GVHD have confirmed the safety and feasibility of adoptive Treg infusions (128–131). Clinical reports of adoptive infusion of Treg in kidney transplant recipients have demonstrated the safety of this method in solid organ transplantation, and, through the method of isotope plutonium labeling (3H), it has been found that Tregs can still be detectable for up to 1 year after infusion (132, 133).
Currently, multiple transplant centers around the world are conducting clinical trials of liver transplantation Treg treatment. Todo et al. from the Hokkaido University in Japan, studied 10 liver transplant recipients who received a single dose of donor antigen-specific Treg. Tregs from recipient lymphocytes were amplified by co-culture with irradiated donor cells in the presence of anti-CD80/86 monoclonal antibodies in vitro for 2 weeks. CD4 + CD25 + FoxP3 + Tregs were amplified 3–6-fold to 28.1% of CD4 + cells and still maintained inhibitory activity. On the 13th day after the operation, the cells were infused back to the recipient with 0.23~6.37 × 106 cell/Kg intravenously. IS was gradually reduced during 6 months and withdrawn 18 months postoperatively. These recipients were subjected to rigorous monitoring, including liver biopsies, T cell activity assessments, and level of donor-specific antibodies. After 16 to 33 months of follow-up, 7 patients achieved OT without rejection and 4 remained IS-free for 24 months. Mild rejection occurred in 3 patients, and low dose IS was maintained afterward (121).
Safinia et al., at London University (UK), performed a combined I/IIa clinical trial ThRIL (NCT02166177) for the application of Treg immunotherapy in the field of liver transplantation. Tregs were isolated from liver transplant recipients by Good manufacturing practice (GMP) separation technology based on CliniMACS sorting. IL-2 and rapamycin were used for Tregs expansion in vitro. A stable Treg population (purity of CD4 + CD25 + FOXP3 +> 95%) can be obtained in 36 days, reaching a sufficient number for its clinical application (120). With stimulation by rapamycin, the amplified Tregs could maintain high levels of FOXP3, CD127lo, and CTLA4, and, with continued expression of CD62L and CXCR3, ensure the stability and functionality of Treg amplification, which could prevent Treg from transforming into Th17 cells in the presence of pro-inflammatory cytokines (134). Nine liver transplant recipients have received autologous polyclonal Treg infusions, showing that the procedure is safe, does not increase the incidence of infection or cancer, and can temporarily increase circulating Treg pools and reduce anti-donor T cell reaction (135).
The current research has opened the door for adoptive infusion of Treg in liver transplantation induction therapy, showing good application prospects. Subsequent research may need to focus on isolation purity, functional induction, CAR-Treg, and clinical induction protocols for OT of Treg in vitro.
Regulatory Dendritic Cells in Liver Transplant Tolerance
In 1973, Steinman et al. found a cell type with a “star shape,” or dendritic morphology, found in the preparation of adherent spleen cells and named dendritic cell (DC) (136). It has been recognized that DCs are a group of highly heterogeneous cell populations derived from the myeloid or lymphoid, which are widely distributed in all tissues and organs and are the most powerful APC in the body, regulating both innate and adaptive immunity and playing an important role in promoting self-tolerance in healthy homeostasis (137, 138). In humans, according to their cell morphology and function, DCs are divided into two mean lineages of CD11c + conventional DCs (cDCs) (HLA-DR + CD11c +) and CD11c- plasmocyte-like DCs (pDCs) (HLA-DR + CD123 +) (139).
In 1996, Steptoe and Thomson defined the DC population that can induce immune tolerance in vivo as tolerogenic DC (tolDC) (140). However, it is still unclear whether tolDCs constitute a particular lineage or just reflect a specific activation state of DCs (141). In 2003, Sato et al. named the tolerogenic DCs they cultured in vitro as "regulatory DCs (regDC),” because they had the ability to inhibit T cell activation, induce T cell anergy, and induce Tregs. They could also maintain strong immunoregulatory properties in inflammatory conditions and have the potential to resist multiple immune diseases (142, 143). This nomenclature has also been widely used in classic tolerogenic DCs and their derivatives (144–148). Currently, two methods of naming such tolerant DCs are both widely used. Over the past 20 years, a large number of studies have found that regDCs could be used to treat various autoimmune diseases in animal models, such as T1D, SSc, RA, Cohn's Disease, etc. (149–152), and to induce tolerance of in GVHD and allografts (115, 143, 153, 154). They also have good clinical application prospects in the field of liver transplant tolerance (139, 155).
The phenotypic characteristics of regDC include low expression of MHC class I and II molecules and T cell co-stimulatory molecules (CD80/B7.1, CD86/B7.2, CD40, OX40L), T cell co-inhibition of ligands (such as programmed death Ligand 1 PD-L1), high expression of death-inducing ligands (FasL), and low expression of adhesion molecules (156, 157). Unlike immature DCs, there are indications that tolerability of regDCs is the result of a specific transcription program, rather than the preservation of immature status (158).
RegDCs retain the ability to present antigens to specific T cells, and they can also build up peripheral tolerance through different immunoregulatory mechanisms. These related promotion mechanisms include the following:
• T cell anergy and T cell clonal deletion (159, 160);
• Apoptosis in naive and memory T cells through increased expression of Fas (CD95)/FasL and indoleamine 2,3-dioxygenase (IDO) (161, 162);
• Inducing and expanding regulatory lymphocytes, including Tregs (163, 164) and Bregs (165);
• Producing double negative (CD3 [+] CD4 [−] CD8 [−]) T cells (166);
• Development of tolerance by increasing the expression and release of immune regulatory molecules, such as the anti-inflammatory cytokines IL-10, TGF-b, NO, and HO-1 (167–170), the apoptosis-inducing PD-L 1, PD-L2, and human leukocytes Ag-G (HLA-G), and the tumor necrosis factor (TNF) (161, 164, 171, 172).
Recent studies have shown that exosomes released by regDCs are also involved in the induction and maintenance of peripheral T cell tolerance (172–174).
Although DCs are widely distributed in tissues, their proportion is very low. Immature DCs (imDCs) are tolerogenic in the body, but they are also unstable and may differentiate into immunogenic DCs in inflammatory conditions. Therefore, it is very important to establish a mature system for regDC culture in vitro to obtain a sufficient number of functional and stable regDCs.
DCs in the immune system act as “immune checkpoints,” with the key role of turning immune signals on or off. A large number of anti-inflammatory and immunosuppressive mediators can promote tolerogenic phenotypes by interfering with DC differentiation or activating checkpoints (157). Researchers have explored different strategies for generating stable regDCs, some of which have been performed in clinical trials, but a consensus hasn't been reached on the best approach yet (115, 157, 172, 175, 176).
Currently, regDCs in vitro are mainly derived from rodent bone marrow cells and human peripheral blood mononuclear cells, as it is easier and less invasive than to operate in humans, and abundant DC precursors are also available. Granulocyte-macrophage colony-stimulating factor (GM-CSF) ± IL-4 can be added to fresh or frozen blood mononuclear cells or their precursors to promote the differentiation of myeloid tolDCs (143, 175). Then, one or more anti-inflammatory and immunosuppressive agents should also be added to inhibit their maturation and promote tolerance. These agents include anti-inflammatory cytokines (such as IL-10, TGF-β, TNF-α), anti-inflammatory/IS drugs (CNI, rapamycin, mycophenolate, corticosteroids, or aspirin), Vitamin D3, Prostaglandin E2, retinoids, and HLA-G, tissue factors, such as hepatocyte growth factor (HGF) and vasoactive intestinal peptide (VIP), etc. (139, 143, 153, 177–180).
In rodent and non-human primate transplantation models, adoptive infusion of DCreg prior to transplantation can prolong the survival of allografts and promote specific tolerance to the graft either alone, or in combination with short-term IS (144, 154, 181–183). Clinical trials on the safety and effectiveness of regDC have been conducted for a variety of autoimmune diseases, including T1D, RA, multiple sclerosis (MS), Crohn's Disease (184–188) (NCT02618902, NCT02903537, NCT01352858, NCT00445913), and renal transplant rejection (137) (NCT 0364265, NCT02252055). So far, although there are no long-term results, it has been confirmed that a regDC regimen is safe and feasible without significant side effects, and that the patient's compliance is good. These results provide a good theoretical guide for a regDC therapeutic schedule for liver transplantation.
In Pittsburgh University (USA), Thomson et al. performed a single-center, phase I/II clinical trial on regDC in living donor liver transplantation (NCT03164265). The study recruited low-risk living donor liver transplantation (LDLT) recipients, isolated monocytes from peripheral blood from potential living organ donors, and cultured cells with GM-CSF, IL-4, VitD3, and IL-10 for 7 days in vitro. GMP-grade donor-derived regDCs could be induced (153, 189), and a single intravenous infusion of 2.5–10 × 10 6 donor-derived regDCs/kg was administered 7 days before the surgery. Meanwhile, half a dose of mycophenolic acid (MPA) was given, without ATG or Ab. MPA and Tac were administrated within 6 months after transplantation. At 6 months after transplantation, recipients who meet specific criteria [non-rejection and liver function allowance tests (LFTs)] may gradually discontinue MPA. TAC withdrawal assessments are performed 1 year after transplantation and then discontinued gradually to achieve complete IS withdrawal 18 months after liver transplantation. The recipients will be followed up for 3 years from IS withdrawal. During the follow-up period, clinical data and peripheral blood were regularly collected and analyzed to evaluate changes in liver function, renal function, donor-specific antigen (DSA) levels, cardiovascular risk factors, and quality of life. Meanwhile, liver biopsy is to be performed after 1 and 3 years from the withdrawal of IS (146). This study is still in the research stage, but we are looking forward to the results.
Autologous DCs seem to be more feasible than donor-derived DCs, especially for liver transplantation from deceased donors, as it can avoid the risk of sensitization. Autologous regDC infusion with or without donor antigen pulse has shown good tolerogenic effects in animal transplant model studies (179, 190). Some studies have shown that autologous tolDC is more effective than donor DC in delayed transplant rejection (180, 191). Under the leadership of the European Union, in Nantes University (France), Moreau A. et al. conducted a Phase I/II (feasibility/safety) “one study” (www. onestudy.org) on kidney transplant recipients with autologous tolDCs infusion (NCT0225055) (192), and its clinical effects are still being observed.
There are few clinical trials about regDC in the induction of liver transplantation tolerance, and still in the observation stage up to now. As a kind of powerful immune-regulating cell, the prospect of regDC is still thrilling in liver transplantation tolerance. For the successful conversion from preclinical researches to clinical application, researches still have many issues to be studied extensively, such as the further optimization of the regDC induction scheme to extend its half-life, the stability of immunomodulatory function, and the administration scheme of IS. However, the further exploration of methods to induce immune tolerance will also improve our understanding of the biological characteristics of DC and the mechanisms of tolerance.
Summary and Future Development
Immune tolerance has always been the “holy grail” in the field of organ transplantation. On the basis of a large number of preclinical studies, various cell therapies could hold promising prospects for inducing liver tolerance. This article reviews the related research and progress regarding spontaneous tolerance and the HSCT, Tregs, and regDCs strategies in the field of liver transplant tolerance. There are many other cells not reviewed that may also have the potential to induce liver transplant tolerance, such as mesenchymal stem cells, regulatory macrophages, regulatory B cells, and bone marrow-derived immunosuppressive cells. At present, the clinical trials of various cell therapies are still in the early stages, and most of them are single-center studies. Thus, there is no clear clinical effect, the purity and stability of cell-induced therapy and its safety for long-term recipients should still be explored for a long time, as many issues need to be observed.
The immune system is extremely delicate and complex. It may be difficult to achieve immune tolerance using only one type of tolerant cell or one mechanism. It may be necessary to consider different mechanisms in combination with different immune cells or drugs. The development of immunologic surveillance and tolerance markers is also critical. This could develop personalized tolerance induction programs for transplant recipients and could guide the timing of immunosuppressive drug withdrawal or early detection of rejection, infection, or tumors.
With the in-depth development of multi-field, multi-disciplinary, and multi-level research, the application of various new experimental methods can provide more possibilities and theoretical guidance for liver transplant tolerance. With the development of multi-center clinical trials, we are optimistic about the good prospects for liver transplant tolerance.
Author Contributions
ZC devised this topic. XD wrote the manuscript. ZC, SC, WG, and SZ helped to revise the manuscript. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by National Natural Science Foundation of China (No. 81873511).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Abbreviations
IS, immunosuppression; OT, operational tolerance; APC, antigen-presenting cells; NK cells, natural killer cells; PBMC, peripheral blood mononuclear cells; HSCs, hematopoietic stem cells; HSCT, hematopoietic stem cell transplantation; GVHD, graft vs. host disease; Tregs, regulatory T cells; DC, dendritic cells; regDC, regulatory dendritic cells; tolDC, tolerogenic dendritic cells; GM-CSF, granulocyte-macrophage colony-stimulating factor; GMP, Good manufacturing practice.
References
1. Starzl TE. The long reach of liver transplantation. Nat Med. (2012) 18:1489–92. doi: 10.1038/nm.2927
2. Rabkin JM, de La Melena V, Orloff SL, Corless CL, Rosen HR, Olyaei AJ. Late mortality after orthotopic liver transplantation. Am J Surg. (2001) 181:475–9. doi: 10.1016/S0002-9610(01)00595-5
3. Dopazo C, Bilbao I, Castells LL, Sapisochin G, Moreiras C, Campos-Varela I, et al. Analysis of adult 20-year survivors after liver transplantation. Hepatol Int. (2015) 9:461–70. doi: 10.1007/s12072-014-9577-x
4. Lechler RI, Sykes M, Thomson AW, Turka LA. Organ transplantation–how much of the promise has been realized? Nat Med. (2005) 11:605–13. doi: 10.1038/nm1251
5. Calne RY. Prope tolerance–the future of organ transplantation from the laboratory to the clinic. Int Immunopharmacol. (2005) 5:163–7. doi: 10.1016/j.intimp.2004.09.026
6. Calne RY. The future of organ transplantation: from the laboratory to the clinic. Philos Trans R Soc Lond B Biol Sci. (2001) 356:767–71. doi: 10.1098/rstb.2001.0848
7. Crispe IN. Immune tolerance in liver disease. Hepatology. (2014) 60:2109–17. doi: 10.1002/hep.27254
8. Calne RY, Sells RA, Pena JR, Davis DR, Millard PR, Herbertson BM, et al. Induction of immunological tolerance by porcine liver allografts. Nature. (1969) 223:472–6. doi: 10.1038/223472a0
9. Jenne CN, Kubes P. Immune surveillance by the liver. Nat Immunol. (2013) 14:996–1006. doi: 10.1038/ni.2691
10. Thomson AW, Knolle PA. Antigen-presenting cell function in the tolerogenic liver environment. Nat Rev Immunol. (2010) 10:753–66. doi: 10.1038/nri2858
11. Lumsden AB, Henderson JM, Kutner MH. Endotoxin levels measured by a chromogenic assay in portal, hepatic and peripheral venous blood in patients with cirrhosis. Hepatology. (1988) 8:232–6. doi: 10.1002/hep.1840080207
12. Feng S. Spontaneous and induced tolerance for liver transplant recipients. Curr Opin Organ Transplant. (2016) 21:53–8. doi: 10.1097/MOT.0000000000000268
13. Reyes J, Zeevi A, Ramos H, Tzakis A, Todo S, Demetris AJ, et al. Frequent achievement of a drug-free state after orthotopic liver transplantation. Transplant Proc. (1993) 25:3315–9.
14. Mazariegos GV, Reyes J, Marino I, Flynn B, Fung JJ, Starzl TE. Risks and benefits of weaning immunosuppression in liver transplant recipients: long-term follow-up. Transplant Proc. (1997) 29:1174–7. doi: 10.1016/S0041-1345(96)00535-0
15. Devlin J, Doherty D, Thomson L, Wong T, Donaldson P, Portmann B, et al. Defining the outcome of immunosuppression withdrawal after liver transplantation. Hepatology. (1998) 27:926–33. doi: 10.1002/hep.510270406
16. Girlanda R, Rela M, Williams R, O'Grady JG, Heaton ND. Long-term outcome of immunosuppression withdrawal after liver transplantation. Transplant Proc. (2005) 37:1708–9. doi: 10.1016/j.transproceed.2005.03.070
17. Takatsuki M, Uemoto S, Inomata Y, Egawa H, Kiuchi T, Fujita S, et al. Weaning of immunosuppression in living donor liver transplant recipients. Transplantation. (2001) 72:449–54. doi: 10.1097/00007890-200108150-00016
18. Oike F, Yokoi A, Nishimura E, Ogura Y, Fujimoto Y, Kasahara M, et al. Complete withdrawal of immunosuppression in living donor liver transplantation. Transplant Proc. (2002) 34:1521. doi: 10.1016/S0041-1345(02)02980-9
19. Eason JD, Cohen AJ, Nair S, Alcantera T, Loss GE. Tolerance: is it worth the risk? Transplantation. (2005) 79:1157–9. doi: 10.1097/01.TP.0000162084.46555.10
20. Tryphonopoulos P, Tzakis AG, Weppler D, Garcia-Morales R, Kato T, Madariaga JR, et al. The role of donor bone marrow infusions in withdrawal of immunosuppression in adult liver allotransplantation. Am J Transplant. (2005) 5:608–13. doi: 10.1111/j.1600-6143.2004.00743.x
21. Tryphonopoulos P, Ruiz P, Weppler D, Nishida S, Levi DM, Moon J, et al. Long-term follow-up of 23 operational tolerant liver transplant recipients. Transplantation. (2010) 90:1556–61. doi: 10.1097/TP.0b013e3182003db7
22. Tisone G, Orlando G, Cardillo A, Palmieri G, Manzia TM, Baiocchi L, et al. Complete weaning off immunosuppression in HCV liver transplant recipients is feasible and favourably impacts on the progression of disease recurrence. J Hepatol. (2006) 44:702–9. doi: 10.1016/j.jhep.2005.11.047
23. Orlando G, Manzia T, Baiocchi L, Sanchez-Fueyo A, Angelico M, Tisone G. The Tor Vergata weaning off immunosuppression protocol in stable HCV liver transplant patients: the updated follow up at 78 months. Transplant Immunol. (2008) 20:43–7. doi: 10.1016/j.trim.2008.08.007
24. Assy N, Adams PC, Myers P, Simon V, Minuk GY, Wall W, et al. Randomized controlled trial of total immunosuppression withdrawal in liver transplant recipients: role of ursodeoxycholic acid. Transplantation. (2007) 83:1571–6. doi: 10.1097/01.tp.0000266678.32250.76
25. Pons JA, Ramirez P, Revilla-Nuin B, Pascual D, Baroja-Mazo A, Robles R, et al. Immunosuppression withdrawal improves long-term metabolic parameters, cardiovascular risk factors and renal function in liver transplant patients. Clin Transplant. (2009) 23:329–36. doi: 10.1111/j.1399-0012.2008.00944.x
26. Feng S, Ekong UD, Lobritto SJ, Demetris AJ, Roberts JP, Rosenthal P, et al. Complete immunosuppression withdrawal and subsequent allograft function among pediatric recipients of parental living donor liver transplants. JAMA. (2012) 307:283–93. doi: 10.1001/jama.2011.2014
27. Benitez C, Londono MC, Miquel R, Manzia TM, Abraldes JG, Lozano JJ, et al. Prospective multicenter clinical trial of immunosuppressive drug withdrawal in stable adult liver transplant recipients. Hepatology. (2013) 58:1824–35. doi: 10.1002/hep.26426
28. de la Garza RG, Sarobe P, Merino J, Lasarte JJ, D'Avola D, Belsue V, et al. Trial of complete weaning from immunosuppression for liver transplant recipients: factors predictive of tolerance. Liver Transpl. (2013) 19:937–44. doi: 10.1002/lt.23686
29. Lin NC, Wang HK, Yeh YC, Liu CP, Loong CC, Tsai HL, et al. Minimization or withdrawal of immunosuppressants in pediatric liver transplant recipients. J Pediatr Surg. (2015) 50:2128–33. doi: 10.1016/j.jpedsurg.2015.08.043
30. Feng S, Demetris AJ, Spain KM, Kanaparthi S, Burrell BE, Ekong UD, et al. Five-year histological and serological follow-up of operationally tolerant pediatric liver transplant recipients enrolled in WISP-R. Hepatology. (2017) 65:647–60. doi: 10.1002/hep.28681
31. Jucaud V, Shaked A, DesMarais M, Sayre P, Feng S, Levitsky J, et al. Prevalence and impact of de novo donor-specific antibodies during a multicenter immunosuppression withdrawal trial in adult liver transplant recipients. Hepatology. (2019) 69:1273–86. doi: 10.1002/hep.30281
32. Levitsky J, Burrell BE, Kanaparthi S, Turka LA, Kurian S, Sanchez-Fueyo A, et al. Immunosuppression withdrawal in liver transplant recipients on sirolimus. Hepatology. (2019). doi: 10.1002/hep.31036. [Epub ahead of print].
33. Shaked A, DesMarais MR, Kopetskie H, Feng S, Punch JD, Levitsky J, et al. Outcomes of immunosuppression minimization and withdrawal early after liver transplantation. Am J Transplant. (2019) 19:1397–409. doi: 10.1111/ajt.15205
34. Fairbanks KD, Eustace JA, Fine D, Thuluvath PJ. Renal function improves in liver transplant recipients when switched from a calcineurin inhibitor to sirolimus. Liver Transpl. (2003) 9:1079–85. doi: 10.1053/jlts.2003.50183
35. Turnquist HR, Raimondi G, Zahorchak AF, Fischer RT, Wang Z, Thomson AW. Rapamycin-conditioned dendritic cells are poor stimulators of allogeneic CD4+ T cells, but enrich for antigen-specific Foxp3+ T regulatory cells and promote organ transplant tolerance. J Immunol. (2007) 178:7018–31. doi: 10.4049/jimmunol.178.11.7018
36. Bohne F, Martinez-Llordella M, Lozano JJ, Miquel R, Benitez C, Londono MC, et al. Intra-graft expression of genes involved in iron homeostasis predicts the development of operational tolerance in human liver transplantation. J Clin Invest. (2012) 122:368–82. doi: 10.1172/JCI59411
37. Mazariegos GV, Zahorchak AF, Reyes J, Ostrowski L, Flynn B, Zeevi A, et al. Dendritic cell subset ratio in peripheral blood correlates with successful withdrawal of immunosuppression in liver transplant patients. Am J Transplant. (2003) 3:689–96. doi: 10.1034/j.1600-6143.2003.00109.x
38. Taner T, Martins PN, Ling Q, Ng KT, Huang KT, Eymard C, et al. What is hot and new in basic and translational science in liver transplantation in 2019? Report of the basic and translational research committee of the international liver transplantation society. Transplantation. (2019) 104:516–21. doi: 10.1097/TP.0000000000003058
39. Lerut J, Sanchez-Fueyo A. An appraisal of tolerance in liver transplantation. Am J Transplant. (2006) 6:1774–80. doi: 10.1111/j.1600-6143.2006.01396.x
40. Londono MC, Rimola A, O'Grady J, Sanchez-Fueyo A. Immunosuppression minimization vs. complete drug withdrawal in liver transplantation. J Hepatol. (2013) 59:872–9. doi: 10.1016/j.jhep.2013.04.003
41. Fouquet V, Alves A, Branchereau S, Grabar S, Debray D, Jacquemin E, et al. Long-term outcome of pediatric liver transplantation for biliary atresia: a 10-year follow-up in a single center. Liver Transpl. (2005) 11:152–60. doi: 10.1002/lt.20358
42. Evans HM, Kelly DA, McKiernan PJ, Hubscher S. Progressive histological damage in liver allografts following pediatric liver transplantation. Hepatology. (2006) 43:1109–17. doi: 10.1002/hep.21152
43. Ekong UD, Melin-Aldana H, Seshadri R, Lokar J, Harris D, Whitington PF, et al. Graft histology characteristics in long-term survivors of pediatric liver transplantation. Liver Transpl. (2008) 14:1582–7. doi: 10.1002/lt.21549
44. Hubscher S. What does the long-term liver allograft look like for the pediatric recipient? Liver Transpl. (2009) 15(Suppl. 2):S19–24. doi: 10.1002/lt.21902
45. Scheenstra R, Peeters PM, Verkade HJ, Gouw AS. Graft fibrosis after pediatric liver transplantation: ten years of follow-up. Hepatology. (2009) 49:880–6. doi: 10.1002/hep.22686
46. Yoshitomi M, Koshiba T, Haga H, Li Y, Zhao X, Cheng D, et al. Requirement of protocol biopsy before and after complete cessation of immunosuppression after liver transplantation. Transplantation. (2009) 87:606–14. doi: 10.1097/TP.0b013e318195a7cb
47. Banff Working Group on Liver Allograft P. Importance of liver biopsy findings in immunosuppression management: biopsy monitoring and working criteria for patients with operational tolerance. Liver Transpl. (2012) 18:1154–70. doi: 10.1002/lt.23481
48. Miyagawa-Hayashino A, Yoshizawa A, Uchida Y, Egawa H, Yurugi K, Masuda S, et al. Progressive graft fibrosis and donor-specific human leukocyte antigen antibodies in pediatric late liver allografts. Liver Transpl. (2012) 18:1333–42. doi: 10.1002/lt.23534
49. Briem-Richter A, Ganschow R, Sornsakrin M, Brinkert F, Schirmer J, Schaefer H, et al. Liver allograft pathology in healthy pediatric liver transplant recipients. Pediatr Transplant. (2013) 17:543–9. doi: 10.1111/petr.12119
50. Demetris AJ, Isse K. Tissue biopsy monitoring of operational tolerance in liver allograft recipients. Curr Opin Organ Transplant. (2013) 18:345–53. doi: 10.1097/MOT.0b013e3283615d48
51. Feng S, Bucuvalas JC, Demetris AJ, Burrell BE, Spain KM, Kanaparthi S, et al. Evidence of chronic allograft injury in liver biopsies from long-term pediatric recipients of liver transplants. Gastroenterology. (2018) 155:1838–51 e7. doi: 10.1053/j.gastro.2018.08.023
52. Venturi C, Sempoux C, Quinones JA, Bourdeaux C, Hoyos SP, Sokal E, et al. Dynamics of allograft fibrosis in pediatric liver transplantation. Am J Transplant. (2014) 14:1648–56. doi: 10.1111/ajt.12740
53. Londono MC, Souza LN, Lozano JJ, Miquel R, Abraldes JG, Llovet LP, et al. Molecular profiling of subclinical inflammatory lesions in long-term surviving adult liver transplant recipients. J Hepatol. (2018) 69:626–34. doi: 10.1016/j.jhep.2018.04.012
54. Owen RD. Immunogenetic consequences of vascular anastomoses between bovine twins. Science. (1945) 102:400–1. doi: 10.1126/science.102.2651.400
55. Kashiwagi N, Porter KA, Penn I, Brettschneider L, Starzl TE. Studies of homograft sex and of gamma globulin phenotypes after orthotopic homotransplantation of the human liver. Surg Forum. (1969) 20:374–6.
56. Till JE, Mc CE. A direct measurement of the radiation sensitivity of normal mouse bone marrow cells. Radiat Res. (1961) 14:213–22.
57. Becker AJ, Mc CE, Till JE. Cytological demonstration of the clonal nature of spleen colonies derived from transplanted mouse marrow cells. Nature. (1963) 197:452–4. doi: 10.1038/197452a0
58. Seita J, Weissman IL. Hematopoietic stem cell: self-renewal vs. differentiation. Wiley Interdiscip Rev Syst Biol Med. (2010) 2:640–53. doi: 10.1002/wsbm.86
59. Starzl TE, Demetris AJ, Trucco M, Murase N, Ricordi C, Ildstad S, et al. Cell migration and chimerism after whole-organ transplantation: the basis of graft acceptance. Hepatology. (1993) 17:1127–52. doi: 10.1002/hep.1840170629
60. Sykes M. Hematopoietic cell transplantation for tolerance induction: animal models to clinical trials. Transplantation. (2009) 87:309–16. doi: 10.1097/TP.0b013e31819535c2
61. Jenq RR, van den Brink MR. Allogeneic haematopoietic stem cell transplantation: individualized stem cell and immune therapy of cancer. Nat Rev Cancer. (2010) 10:213–21. doi: 10.1038/nrc2804
62. Daikeler T, Tichelli A, Passweg J. Complications of autologous hematopoietic stem cell transplantation for patients with autoimmune diseases. Pediatr Res. (2012) 71(4 Pt 2):439–44. doi: 10.1038/pr.2011.57
63. Muraro PA, Robins H, Malhotra S, Howell M, Phippard D, Desmarais C, et al. T cell repertoire following autologous stem cell transplantation for multiple sclerosis. J Clin Invest. (2014) 124:1168–72. doi: 10.1172/JCI71691
64. Notta F, Doulatov S, Laurenti E, Poeppl A, Jurisica I, Dick JE. Isolation of single human hematopoietic stem cells capable of long-term multilineage engraftment. Science. (2011) 333:218–21. doi: 10.1126/science.1201219
65. Pelus LM. Peripheral blood stem cell mobilization: new regimens, new cells, where do we stand. Curr Opin Hematol. (2008) 15:285–92. doi: 10.1097/MOH.0b013e328302f43a
66. Khan A, Tomita Y, Sykes M. Thymic dependence of loss of tolerance in mixed allogeneic bone marrow chimeras after depletion of donor antigen. Peripheral mechanisms do not contribute to maintenance of tolerance. Transplantation. (1996) 62:380–7. doi: 10.1097/00007890-199608150-00014
67. Elahimehr R, Scheinok AT, McKay DB. Hematopoietic stem cells and solid organ transplantation. Transplant Rev. (2016) 30:227–34. doi: 10.1016/j.trre.2016.07.005
68. Wekerle T, Blaha P, Koporc Z, Bigenzahn S, Pusch M, Muehlbacher F. Mechanisms of tolerance induction through the transplantation of donor hematopoietic stem cells: central vs. peripheral tolerance. Transplantation (2003) 75(Suppl. 9):21S-5S. doi: 10.1097/01.TP.0000067947.90241.66
69. Mueller DL. Mechanisms maintaining peripheral tolerance. Nat Immunol. (2010) 11:21–7. doi: 10.1038/ni.1817
70. Xing Y, Hogquist KA. T-cell tolerance: central and peripheral. Cold Spring Harb Perspect Biol. (2012) 4. doi: 10.1101/cshperspect.a006957
71. Salisbury EM, Game DS, Lechler RI. Transplantation tolerance. Pediatr Nephrol. (2014) 29:2263–72. doi: 10.1007/s00467-013-2659-5
72. Wood KJ. Passenger leukocytes and microchimerism: what role in tolerance induction? Transplantation. (2003) 75(Suppl. 9):17s−20. doi: 10.1097/01.TP.0000067946.90241.2F
73. Szabolcs P, Burlingham WJ, Thomson AW. Tolerance after solid organ and hematopoietic cell transplantation. Biol Blood Marrow Transplant. (2012) 18(Suppl. 1):S193–200. doi: 10.1016/j.bbmt.2011.11.005
74. Copelan EA. Hematopoietic stem-cell transplantation. N Engl J Med. (2006) 354:1813–26. doi: 10.1056/NEJMra052638
75. Sachs DH, Kawai T, Sykes M. Induction of tolerance through mixed chimerism. Cold Spring Harb Perspect Med. (2014) 4:a015529. doi: 10.1101/cshperspect.a015529
76. Fuchs EJ. Transplantation tolerance: from theory to clinic. Immunol Rev. (2014) 258:64–79. doi: 10.1111/imr.12154
77. Cobbold SP, Martin G, Qin S, Waldmann H. Monoclonal antibodies to promote marrow engraftment and tissue graft tolerance. Nature. (1986) 323:164–6. doi: 10.1038/323164a0
78. Wekerle T, Kurtz J, Ito H, Ronquillo JV, Dong V, Zhao G, et al. Allogeneic bone marrow transplantation with co-stimulatory blockade induces macrochimerism and tolerance without cytoreductive host treatment. Nat Med. (2000) 6:464–9. doi: 10.1038/74731
79. Sykes M, Sachs DH. Mixed chimerism. Philos Trans R Soc Lond B Biol Sci. (2001) 356:707–26. doi: 10.1098/rstb.2001.0853
80. Kawai T, Cosimi AB, Spitzer TR, Tolkoff-Rubin N, Suthanthiran M, Saidman SL, et al. HLA-mismatched renal transplantation without maintenance immunosuppression. N Engl J Med. (2008) 358:353–61. doi: 10.1056/NEJMoa071074
81. Kawai T, Sachs DH, Sykes M, Cosimi AB. HLA-mismatched renal transplantation without maintenance immunosuppression. N Engl J Med. (2013) 368:1850–2. doi: 10.1056/NEJMc1213779
82. Leventhal JR, Elliott MJ, Yolcu ES, Bozulic LD, Tollerud DJ, Mathew JM, et al. Immune reconstitution/immunocompetence in recipients of kidney plus hematopoietic stem/facilitating cell transplants. Transplantation. (2015) 99:288–98. doi: 10.1097/TP.0000000000000605
83. Scandling JD, Busque S, Shizuru JA, Lowsky R, Hoppe R, Dejbakhsh-Jones S, et al. Chimerism, graft survival, and withdrawal of immunosuppressive drugs in HLA matched and mismatched patients after living donor kidney and hematopoietic cell transplantation. Am J Transplant. (2015) 15:695–704. doi: 10.1111/ajt.13091
84. Ringden O, Soderdahl G, Mattsson J, Uzunel M, Remberger M, Hentschke P, et al. Transplantation of autologous and allogeneic bone marrow with liver from a cadaveric donor for primary liver cancer. Transplantation. (2000) 69:2043–8. doi: 10.1097/00007890-200005270-00012
85. Donckier V, Troisi R, Toungouz M, Colle I, Van Vlierberghe H, Jacquy C, et al. Donor stem cell infusion after non-myeloablative conditioning for tolerance induction to HLA mismatched adult living-donor liver graft. Transplant Immunol. (2004) 13:139–46. doi: 10.1016/j.trim.2004.05.004
86. Donckier V, Troisi R, Le Moine A, Toungouz M, Ricciardi S, Colle I, et al. Early immunosuppression withdrawal after living donor liver transplantation and donor stem cell infusion. Liver Transpl. (2006) 12:1523–8. doi: 10.1002/lt.20872
87. Alexander SI, Smith N, Hu M, Verran D, Shun A, Dorney S, et al. Chimerism and tolerance in a recipient of a deceased-donor liver transplant. N Engl J Med. (2008) 358:369–74. doi: 10.1056/NEJMoa0707255
88. Alexander T, Arnold R, Hiepe F, Radbruch A. Resetting the immune system with immunoablation and autologous haematopoietic stem cell transplantation in autoimmune diseases. Clin Exp Rheumatol. (2016) 34(4 Suppl. 98):53–7.
89. Arruda LC, Clave E, Moins-Teisserenc H, Douay C, Farge D, Toubert A. Resetting the immune response after autologous hematopoietic stem cell transplantation for autoimmune diseases. Curr Res Transl Med. (2016) 64:107–13. doi: 10.1016/j.retram.2016.03.004
90. Snowden JA, Saccardi R, Allez M, Ardizzone S, Arnold R, Cervera R, et al. Haematopoietic SCT in severe autoimmune diseases: updated guidelines of the European Group for Blood and Marrow Transplantation. Bone Marrow Transplant. (2012) 47:770–90. doi: 10.1038/bmt.2011.185
91. Sun W, Popat U, Hutton G, Zang YC, Krance R, Carrum G, et al. Characteristics of T-cell receptor repertoire and myelin-reactive T cells reconstituted from autologous haematopoietic stem-cell grafts in multiple sclerosis. Brain. (2004) 127(Pt 5):996–1008. doi: 10.1093/brain/awh117
92. Farge D, Henegar C, Carmagnat M, Daneshpouy M, Marjanovic Z, Rabian C, et al. Analysis of immune reconstitution after autologous bone marrow transplantation in systemic sclerosis. Arthritis Rheum. (2005) 52:1555–63. doi: 10.1002/art.21036
93. Alexander T, Thiel A, Rosen O, Massenkeil G, Sattler A, Kohler S, et al. Depletion of autoreactive immunologic memory followed by autologous hematopoietic stem cell transplantation in patients with refractory SLE induces long-term remission through de novo generation of a juvenile and tolerant immune system. Blood. (2009) 113:214–23. doi: 10.1182/blood-2008-07-168286
94. Dubinsky AN, Burt RK, Martin R, Muraro PA. T-cell clones persisting in the circulation after autologous hematopoietic SCT are undetectable in the peripheral CD34+ selected graft. Bone Marrow Transplant. (2010) 45:325–31. doi: 10.1038/bmt.2009.139
95. Malmegrim KCR, Lima-Júnior JR, Arruda LCM, de Azevedo JTC, de Oliveira GLV, Oliveira MC. Autologous hematopoietic stem cell transplantation for autoimmune diseases: from mechanistic insights to biomarkers. Front Immunol. (2018) 9:02602. doi: 10.3389/fimmu.2018.02602
96. de Kleer I, Vastert B, Klein M, Teklenburg G, Arkesteijn G, Yung GP, et al. Autologous stem cell transplantation for autoimmunity induces immunologic self-tolerance by reprogramming autoreactive T cells and restoring the CD4+CD25+ immune regulatory network. Blood. (2006) 107:1696–702. doi: 10.1182/blood-2005-07-2800
97. Abrahamsson SV, Angelini DF, Dubinsky AN, Morel E, Oh U, Jones JL, et al. Non-myeloablative autologous haematopoietic stem cell transplantation expands regulatory cells and depletes IL-17 producing mucosal-associated invariant T cells in multiple sclerosis. Brain. (2013) 136(Pt 9):2888–903. doi: 10.1093/brain/awt182
98. Hendrawan K, Visweswaran M, Ma DDF, Moore JJ. Tolerance regeneration by T regulatory cells in autologous haematopoietic stem cell transplantation for autoimmune diseases. Bone Marrow Transplant. (2019) 55:857–66. doi: 10.1038/s41409-019-0710-2
99. Zhang L, Bertucci AM, Ramsey-Goldman R, Burt RK, Datta SK. Regulatory T cell (Treg) subsets return in patients with refractory lupus following stem cell transplantation, and TGF-beta-producing CD8+ Treg cells are associated with immunological remission of lupus. J Immunol. (2009) 183:6346–58. doi: 10.4049/jimmunol.0901773
100. Arruda LCM, Oliveira MC, Moraes DA, Covas DT, Voltarelli JC, Malmegrim KCR. THU0501 hematopoietic stem cell transplantation increases naive and regulatory B cells while decreasing memory B cells in systemic sclerosis patients. Ann Rheum Dis. (2014) 73:492–509. doi: 10.1136/annrheumdis-2014-eular.4148
101. Snowden JA, Passweg J, Moore JJ, Milliken S, Cannell P, Van Laar J, et al. Autologous hemopoietic stem cell transplantation in severe rheumatoid arthritis: a report from the EBMT and ABMTR. J Rheumatol. (2004) 31:482–8.
102. Burt RK, Shah SJ, Dill K, Grant T, Gheorghiade M, Schroeder J, et al. Autologous non-myeloablative haemopoietic stem-cell transplantation compared with pulse cyclophosphamide once per month for systemic sclerosis (ASSIST): an open-label, randomised phase 2 trial. Lancet. (2011) 378:498–506. doi: 10.1016/S0140-6736(11)60982-3
103. Hawkey CJ. Hematopoietic stem cell transplantation in crohn's disease: state-of-the-art treatment. Digest Dis. (2017) 35:107–14. doi: 10.1159/000449090
104. Leone A, Radin M, Almarzooqi AM, Al-Saleh J, Roccatello D, Sciascia S, et al. Autologous hematopoietic stem cell transplantation in systemic lupus erythematosus and antiphospholipid syndrome: a systematic review. Autoimmunity Rev. (2017) 16:469–77. doi: 10.1016/j.autrev.2017.03.008
105. van Megen KM, van 't Wout ET, Forman SJ, Roep BO. A future for autologous hematopoietic stem cell transplantation in type 1 diabetes. Front Immunol. (2018) 9:690. doi: 10.3389/fimmu.2018.00690
106. Terai S, Ishikawa T, Omori K, Aoyama K, Marumoto Y, Urata Y, et al. Improved liver function in patients with liver cirrhosis after autologous bone marrow cell infusion therapy. Stem Cells. (2006) 24:2292–8. doi: 10.1634/stemcells.2005-0542
107. Pai M, Zacharoulis D, Milicevic MN, Helmy S, Jiao LR, Levicar N, et al. Autologous infusion of expanded mobilized adult bone marrow-derived CD34+ cells into patients with alcoholic liver cirrhosis. Am J Gastroenterol. (2008) 103:1952–8. doi: 10.1111/j.1572-0241.2008.01993.x
108. Saito T, Okumoto K, Haga H, Nishise Y, Ishii R, Sato C, et al. Potential therapeutic application of intravenous autologous bone marrow infusion in patients with alcoholic liver cirrhosis. Stem Cells Dev. (2011) 20:1503–10. doi: 10.1089/scd.2011.0074
109. Pankaj P, Zhang Q, Bai XL, Liang TB. Autologous bone marrow transplantation in decompensated liver: systematic review and meta-analysis. World J Gastroenterol. (2015) 21:8697–710. doi: 10.3748/wjg.v21.i28.8697
110. Gorczynski R, Chen Z, Khatri I, Yu K. Long-term tolerance and skin allograft survival in cd200tg mice after autologous marrow transplantation. Transplantation. (2014) 98:1271–8. doi: 10.1097/TP.0000000000000456
111. Gorczynski RM, Sadozai H, Zhu F, Khatri I. Effect of infusion of monoclonal antibodies to tumour necrosis factor-receptor super family 25 on graft rejection in allo-immune mice receiving autologous marrow transplantation. Immunology. (2017) 150:418–31. doi: 10.1111/imm.12693
112. Gorczynski RM, Farrokhi K, Gorczynski C, Sadozai H, Zhu F, Khatri I. Importance of B cells to development of regulatory T cells and prolongation of tissue allograft survival in recipients receiving autologous bone marrow transplantation. Immunology. (2018) 154:465–75. doi: 10.1111/imm.12895
113. Vaikunthanathan T, Safinia N, Boardman D, Lechler RI, Lombardi G. Regulatory T cells: tolerance induction in solid organ transplantation. Clin Exp Immunol. (2017) 189:197–210. doi: 10.1111/cei.12978
114. Vignali DAA, Collison LW, Workman CJ. How regulatory T cells work. Nat Rev Immunol. (2008) 8:523–32. doi: 10.1038/nri2343
115. Ten Brinke A, Martinez-Llordella M, Cools N, Hilkens CMU, van Ham SM, Sawitzki B, et al. Ways forward for tolerance-inducing cellular therapies- an AFACTT perspective. Front Immunol. (2019) 10:181. doi: 10.3389/fimmu.2019.00181
116. Li W, Zheng XX, Kuhr CS, Perkins JD. CTLA4 engagement is required for induction of murine liver transplant spontaneous tolerance+. Am J Transpl. (2005) 5:978–86. doi: 10.1111/j.1600-6143.2005.00823.x
117. Fujiki M, Esquivel CO, Martinez OM, Strober S, Uemoto S, Krams SM. Induced tolerance to rat liver allografts involves the apoptosis of intragraft T cells and the generation of CD4+CD25+FoxP3+T regulatory cells. Liver Transpl. (2010) 16:147–54. doi: 10.1002/lt.21963
118. Li Y, Zhao X, Cheng D, Haga H, Tsuruyama T, Wood K, et al. The presence of Foxp3 expressing T cells within grafts of tolerant human liver transplant recipients. Transplantation. (2008) 86:1837–43. doi: 10.1097/TP.0b013e31818febc4
119. Pons JA, Revilla-Nuin B, Baroja-Mazo A, Ramirez P, Martinez-Alarcon L, Sanchez-Bueno F, et al. FoxP3 in peripheral blood is associated with operational tolerance in liver transplant patients during immunosuppression withdrawal. Transplantation. (2008) 86:1370–8. doi: 10.1097/TP.0b013e318188d3e6
120. Safinia N, Vaikunthanathan T, Fraser H, Thirkell S, Lowe K, Blackmore L, et al. Successful expansion of functional and stable regulatory T cells for immunotherapy in liver transplantation. Oncotarget. (2016) 7:7563–77. doi: 10.18632/oncotarget.6927
121. Todo S, Yamashita K, Goto R, Zaitsu M, Nagatsu A, Oura T, et al. A pilot study of operational tolerance with a regulatory T-cell-based cell therapy in living donor liver transplantation. Hepatology. (2016) 64:632–43. doi: 10.1002/hep.28459
122. Gregori S, Passerini L, Roncarolo MG. Clinical outlook for type-1 and FOXP3(+) T regulatory cell-based therapy. Front Immunol. (2015) 6:593. doi: 10.3389/fimmu.2015.00593
123. van der Net JB, Bushell A, Wood KJ, Harden PN. Regulatory T cells: first steps of clinical application in solid organ transplantation. Transpl Int. (2016) 29:3–11. doi: 10.1111/tri.12608
124. Ellebrecht CT, Bhoj VG, Nace A, Choi EJ, Mao X, Cho MJ, et al. Reengineering chimeric antigen receptor T cells for targeted therapy of autoimmune disease. Science. (2016) 353:179–84. doi: 10.1126/science.aaf6756
125. MacDonald KG, Hoeppli RE, Huang Q, Gillies J, Luciani DS, Orban PC, et al. Alloantigen-specific regulatory T cells generated with a chimeric antigen receptor. J Clin Invest. (2016) 126:1413–24. doi: 10.1172/JCI82771
126. Boardman DA, Philippeos C, Fruhwirth GO, Ibrahim MAA, Hannen RF, Cooper D, et al. Expression of a chimeric antigen receptor specific for donor HLA class i enhances the potency of human regulatory t cells in preventing human skin transplant rejection. Am J Transpl. (2017) 17:931–43. doi: 10.1111/ajt.14185
127. Noyan F, Zimmermann K, Hardtke-Wolenski M, Knoefel A, Schulde E, Geffers R, et al. Prevention of allograft rejection by use of regulatory T cells with an MHC-specific chimeric antigen receptor. Am J Transpl. (2017) 17:917–30. doi: 10.1111/ajt.14175
128. Desreumaux P, Foussat A, Allez M, Beaugerie L, Hebuterne X, Bouhnik Y, et al. Safety and efficacy of antigen-specific regulatory T-cell therapy for patients with refractory Crohn's disease. Gastroenterology. (2012) 143:1207–17.e2. doi: 10.1053/j.gastro.2012.07.116
129. Theil A, Tuve S, Oelschlagel U, Maiwald A, Dohler D, Ossmann D, et al. Adoptive transfer of allogeneic regulatory T cells into patients with chronic graft-versus-host disease. Cytotherapy. (2015) 17:473–86. doi: 10.1016/j.jcyt.2014.11.005
130. Bayry J, Gautier JF. Regulatory T cell immunotherapy for type 1 diabetes: a step closer to success? Cell Metab. (2016) 23:231–3. doi: 10.1016/j.cmet.2016.01.010
131. Thonhoff JR, Beers DR, Zhao W, Pleitez M, Simpson EP, Berry JD, et al. Expanded autologous regulatory T-lymphocyte infusions in ALS. Neurol Neuroimmunol Neuroinflamm. (2018) 5:e465. doi: 10.1212/NXI.0000000000000465
132. Chandran S, Tang Q, Sarwal M, Laszik ZG, Putnam AL, Lee K, et al. Polyclonal regulatory T cell therapy for control of inflammation in kidney transplants. Am J Transplant. (2017) 17:2945–54. doi: 10.1111/ajt.14415
133. Mathew JM, J HV, LeFever A, Konieczna I, Stratton C, He J, et al. A phase I clinical trial with ex vivo expanded recipient regulatory t cells in living donor kidney transplants. Sci Rep. (2018) 8:7428. doi: 10.1038/s41598-018-25574-7
134. Fraser H, Safinia N, Grageda N, Thirkell S, Lowe K, Fry LJ, et al. A rapamycin-based GMP-compatible process for the isolation and expansion of regulatory T cells for clinical trials. Mol Ther Methods Clin Dev. (2018) 8:198–209. doi: 10.1016/j.omtm.2018.01.006
135. Sanchez-Fueyo A, Whitehouse G, Grageda N, Cramp ME, Lim TY, Romano M, et al. Applicability, safety, and biological activity of regulatory T cell therapy in liver transplantation. Am J Transplant. (2019) 20:1125–36. doi: 10.1111/ajt.15700
136. Steinman RM, Cohn ZA. Identification of a novel cell type in peripheral lymphoid organs of mice. I. morphology, quantitation, tissue distribution. J Exp Med. (1973) 137:1142–62. doi: 10.1084/jem.137.5.1142
137. Banchereau J, Steinman RM. Dendritic cells and the control of immunity. Nature. (1998) 392:245–52. doi: 10.1038/32588
138. Ohnmacht C, Pullner A, King SB, Drexler I, Meier S, Brocker T, et al. Constitutive ablation of dendritic cells breaks self-tolerance of CD4 T cells and results in spontaneous fatal autoimmunity. J Exp Med. (2009) 206:549–59. doi: 10.1084/jem.20082394
139. Sato K, Fujita S. Dendritic cells: nature and classification. Allergol Int. (2007) 56:183–91. doi: 10.2332/allergolint.R-06-139
140. Steptoe RJ, Thomson AW. Dendritic cells and tolerance induction. Clin Exp Immunol. (1996) 105:397–402. doi: 10.1046/j.1365-2249.1996.d01-779.x
141. Takenaka MC, Quintana FJ. Tolerogenic dendritic cells. Semin Immunopathol. (2017) 39:113–20. doi: 10.1007/s00281-016-0587-8
142. Sato K, Yamashita N, Baba M, Matsuyama T. Modified myeloid dendritic cells act as regulatory dendritic cells to induce anergic and regulatory T cells. Blood. (2003) 101:3581–9. doi: 10.1182/blood-2002-09-2712
143. Sato K, Yamashita N, Yamashita N, Baba M, Matsuyama T. Regulatory dendritic cells protect mice from murine acute graft-versus-host disease and leukemia relapse. Immunity. (2003) 18:367–79. doi: 10.1016/S1074-7613(03)00055-4
144. Ezzelarab MB, Zahorchak AF, Lu L, Morelli AE, Chalasani G, Demetris AJ, et al. Regulatory dendritic cell infusion prolongs kidney allograft survival in nonhuman primates. Am J Transplant. (2013) 13:1989–2005. doi: 10.1111/ajt.12310
145. Raich-Regue D, Glancy M, Thomson AW. Regulatory dendritic cell therapy: from rodents to clinical application. Immunol Lett. (2014) 161:216–21. doi: 10.1016/j.imlet.2013.11.016
146. Thomson AW, Humar A, Lakkis FG, Metes DM. Regulatory dendritic cells for promotion of liver transplant operational tolerance: Rationale for a clinical trial and accompanying mechanistic studies. Hum Immunol. (2018) 79:314–21. doi: 10.1016/j.humimm.2017.10.017
147. Thomson AW, Metes DM, Ezzelarab MB, Raïch-Regué D. Regulatory dendritic cells for human organ transplantation. Transplant Rev. (2019) 33:130–6. doi: 10.1016/j.trre.2019.05.001
148. Yu H, Tian Y, Wang Y, Mineishi S, Zhang Y. Dendritic cell regulation of graft-vs.-host disease: immunostimulation and tolerance. Front Immunol. (2019) 10: 93. doi: 10.3389/fimmu.2019.00093
149. Lutz MB, Suri RM, Niimi M, Ogilvie AL, Kukutsch NA, Rossner S, et al. Immature dendritic cells generated with low doses of GM-CSF in the absence of IL-4 are maturation resistant and prolong allograft survival in vivo. Eur J Immunol. (2000) 30:1813–22. doi: 10.1002/1521-4141(200007)30:7<1813::AID-IMMU1813>3.0.CO;2-8
150. Thomson AW, Robbins PD. Tolerogenic dendritic cells for autoimmune disease and transplantation. Ann Rheum Dis. (2008) 67(Suppl. 3):iii90–6. doi: 10.1136/ard.2008.099176
151. Natarajan S, Thomson AW. Tolerogenic dendritic cells and myeloid-derived suppressor cells: potential for regulation and therapy of liver auto- and alloimmunity. Immunobiology. (2010) 215:698–703. doi: 10.1016/j.imbio.2010.05.024
152. Stoop JN, Robinson JH, Hilkens CM. Developing tolerogenic dendritic cell therapy for rheumatoid arthritis: what can we learn from mouse models? Ann Rheum Dis. (2011) 70:1526–33. doi: 10.1136/ard.2011.151654
153. Thomson AW, Zahorchak AF, Ezzelarab MB, Butterfield LH, Lakkis FG, Metes DM. Prospective clinical testing of regulatory dendritic cells in organ transplantation. Front Immunol. (2016) 7:15. doi: 10.3389/fimmu.2016.00015
154. Ezzelarab MB, Raich-Regue D, Lu L, Zahorchak AF, Perez-Gutierrez A, Humar A, et al. Renal allograft survival in nonhuman primates infused with donor antigen-pulsed autologous regulatory dendritic cells. Am J Transplant. (2017) 17:1476–89. doi: 10.1111/ajt.14182
155. Xia MJ, Shan J, Li YP, Zhou YN, Guo YJ, Sun GX, et al. Adoptive transfusion of tolerogenic dendritic cells prolongs the survival of liver allograft: a systematic review. J Evid Based Med. (2014) 7:135–46. doi: 10.1111/jebm.12094
156. Raker VK, Domogalla MP, Steinbrink K. Tolerogenic dendritic cells for regulatory T cell induction in man. Front Immunol. (2015) 6:569. doi: 10.3389/fimmu.2015.00569
157. Sato K, Uto T, Fukaya T, Takagi H. Regulatory dendritic cells. Curr Top Microbiol Immunol. (2017) 410:47–71. doi: 10.1007/82_2017_60
158. Schinnerling K, Garcia-Gonzalez P, Aguillon JC. Gene expression profiling of human monocyte-derived dendritic cells - searching for molecular regulators of tolerogenicity. Front Immunol. (2015) 6:528. doi: 10.3389/fimmu.2015.00528
159. Schwartz RH. T cell anergy. Ann Rev Immunol. (2003) 21:305–34. doi: 10.1146/annurev.immunol.21.120601.141110
160. Schietinger A, Greenberg PD. Tolerance and exhaustion: defining mechanisms of T cell dysfunction. Trends Immunol. (2014) 35:51–60. doi: 10.1016/j.it.2013.10.001
161. Lu L, Qian S, Hershberger PA, Rudert WA, Lynch DH, Thomson AW. Fas ligand (CD95L) and B7 expression on dendritic cells provide counter-regulatory signals for T cell survival and proliferation. J Immunol. (1997) 158:5676–84.
162. Mellor AL, Baban B, Chandler P, Marshall B, Jhaver K, Hansen A, et al. Cutting edge: induced indoleamine 2,3 dioxygenase expression in dendritic cell subsets suppresses T cell clonal expansion. J Immunol. (2003) 171:1652–5. doi: 10.4049/jimmunol.171.4.1652
163. Huang H, Dawicki W, Zhang X, Town J, Gordon JR. Tolerogenic dendritic cells induce CD4+CD25hiFoxp3+ regulatory T cell differentiation from CD4+CD25-/loFoxp3- effector T cells. J Immunol. (2010) 185:5003–10. doi: 10.4049/jimmunol.0903446
164. Hsu SM, Mathew R, Taylor AW, Stein-Streilein J. Ex-vivo tolerogenic F4/80(+) antigen-presenting cells (APC) induce efferent CD8(+) regulatory T cell-dependent suppression of experimental autoimmune uveitis. Clin Exp Immunol. (2014) 176:37–48. doi: 10.1111/cei.12243
165. Qian L, Qian C, Chen Y, Bai Y, Bao Y, Lu L, et al. Regulatory dendritic cells program B cells to differentiate into CD19hiFcgammaIIbhi regulatory B cells through IFN-beta and CD40L. Blood. (2012) 120:581–91. doi: 10.1182/blood-2011-08-377242
166. Hill M, Thebault P, Segovia M, Louvet C, Beriou G, Tilly G, et al. Cell therapy with autologous tolerogenic dendritic cells induces allograft tolerance through interferon-gamma and epstein-barr virus-induced gene 3. Am J Transplant. (2011) 11:2036–45. doi: 10.1111/j.1600-6143.2011.03651.x
167. Chauveau C, Remy S, Royer PJ, Hill M, Tanguy-Royer S, Hubert FX, et al. Heme oxygenase-1 expression inhibits dendritic cell maturation and proinflammatory function but conserves IL-10 expression. Blood. (2005) 106:1694–702. doi: 10.1182/blood-2005-02-0494
168. Ilarregui JM, Croci DO, Bianco GA, Toscano MA, Salatino M, Vermeulen ME, et al. Tolerogenic signals delivered by dendritic cells to T cells through a galectin-1-driven immunoregulatory circuit involving interleukin 27 and interleukin 10. Nat Immunol. (2009) 10:981–91. doi: 10.1038/ni.1772
169. Moreau A, Hill M, Thebault P, Deschamps JY, Chiffoleau E, Chauveau C, et al. Tolerogenic dendritic cells actively inhibit T cells through heme oxygenase-1 in rodents and in nonhuman primates. FASEB J. (2009) 23:3070–7. doi: 10.1096/fj.08-128173
170. Remy S, Blancou P, Tesson L, Tardif V, Brion R, Royer PJ, et al. Carbon monoxide inhibits TLR-induced dendritic cell immunogenicity. J Immunol. (2009) 182:1877–84. doi: 10.4049/jimmunol.0802436
171. Li H, Shi B. Tolerogenic dendritic cells and their applications in transplantation. Cell Mol Immunol. (2015) 12:24–30. doi: 10.1038/cmi.2014.52
172. Ochando J, Ordikhani F, Jordan S, Boros P, Thomson AW. Tolerogenic dendritic cells in organ transplantation. Transpl Int. (2020) 33:113–27. doi: 10.1111/tri.13504
173. Liu Q, Rojas-Canales DM, Divito SJ, Shufesky WJ, Stolz DB, Erdos G, et al. Donor dendritic cell-derived exosomes promote allograft-targeting immune response. J Clin Invest. (2016) 126:2805–20. doi: 10.1172/JCI84577
174. Song J, Huang J, Chen X, Teng X, Song Z, Xing Y, et al. Donor-derived exosomes induce specific regulatory T cells to suppress immune inflammation in the allograft heart. Sci Rep. (2016) 7:20077. doi: 10.1038/srep46389
175. Nestle FO, Banchereau J, Hart D. Dendritic cells: on the move from bench to bedside. Nat Med. (2001) 7:761–5. doi: 10.1038/89863
176. Kryczanowsky F, Raker V, Graulich E, Domogalla MP, Steinbrink K. IL-10-modulated human dendritic cells for clinical use: identification of a stable and migratory subset with improved tolerogenic activity. J Immunol. (2016) 197:3607–17. doi: 10.4049/jimmunol.1501769
177. Adorini L, Penna G, Giarratana N, Uskokovic M. Tolerogenic dendritic cells induced by vitamin D receptor ligands enhance regulatory T cells inhibiting allograft rejection and autoimmune diseases. J Cell Biochem. (2003) 88:227–33. doi: 10.1002/jcb.10340
178. Rutella S, Danese S, Leone G. Tolerogenic dendritic cells: cytokine modulation comes of age. Blood. (2006) 108:1435–40. doi: 10.1182/blood-2006-03-006403
179. Morelli AE, Thomson AW. Tolerogenic dendritic cells and the quest for transplant tolerance. Nat Rev Immunol. (2007) 7:610–21. doi: 10.1038/nri2132
180. Marin E, Cuturi MC, Moreau A. Tolerogenic dendritic cells in solid organ transplantation: where do we stand? Front Immunol. (2018) 9:274. doi: 10.3389/fimmu.2018.00274
181. Fu F, Li Y, Qian S, Lu L, Chambers F, Starzl TE, et al. Costimulatory molecule-deficient dendritic cell progenitors (MHC class II+, CD80dim, CD86-) prolong cardiac allograft survival in nonimmunosuppressed recipients. Transplantation. (1996) 62:659–65. doi: 10.1097/00007890-199609150-00021
182. Zhou Y, Shan J, Guo Y, Li S, Long D, Li Y, et al. Effects of adoptive transfer of tolerogenic dendritic cells on allograft survival in organ transplantation models: an overview of systematic reviews. J Immunol Res. (2016) 2016:5730674. doi: 10.1155/2016/5730674
183. Stead SO, Kireta S, McInnes SJP, Kette FD, Sivanathan KN, Kim J, et al. Murine and non-human primate dendritic cell targeting nanoparticles for in vivo generation of regulatory T-cells. ACS Nano. (2018) 12:6637–47. doi: 10.1021/acsnano.8b01625
184. Giannoukakis N, Phillips B, Finegold D, Harnaha J, Trucco M. Phase I (safety) study of autologous tolerogenic dendritic cells in type 1 diabetic patients. Diabetes Care. (2011) 34:2026–32. doi: 10.2337/dc11-0472
185. Jauregui-Amezaga A, Cabezon R, Ramirez-Morros A, Espana C, Rimola J, Bru C, et al. Intraperitoneal administration of autologous tolerogenic dendritic cells for refractory crohn's disease: a phase I study. J Crohns Colitis. (2015) 9:1071–8. doi: 10.1093/ecco-jcc/jjv144
186. Ten Brinke A, Hilkens CM, Cools N, Geissler EK, Hutchinson JA, Lombardi G, et al. Clinical use of tolerogenic dendritic cells-harmonization approach in european collaborative effort. Mediators Inflamm. (2015) 2015:471719. doi: 10.1155/2015/471719
187. Bell GM, Anderson AE, Diboll J, Reece R, Eltherington O, Harry RA, et al. Autologous tolerogenic dendritic cells for rheumatoid and inflammatory arthritis. Ann Rheum Dis. (2017) 76:227–34. doi: 10.1136/annrheumdis-2015-208456
188. Willekens B, Presas-Rodriguez S, Mansilla MJ, Derdelinckx J, Lee WP, Nijs G, et al. Tolerogenic dendritic cell-based treatment for multiple sclerosis (MS): a harmonised study protocol for two phase I clinical trials comparing intradermal and intranodal cell administration. BMJ Open. (2019) 9:e030309. doi: 10.1136/bmjopen-2019-030309
189. Zahorchak AF, Macedo C, Hamm DE, Butterfield LH, Metes DM, Thomson AW. High PD-L1/CD86 MFI ratio and IL-10 secretion characterize human regulatory dendritic cells generated for clinical testing in organ transplantation. Cell Immunol. (2018) 323:9–18. doi: 10.1016/j.cellimm.2017.08.008
190. Obregon C, Kumar R, Pascual MA, Vassalli G, Golshayan D. Update on dendritic cell-induced immunological and clinical tolerance. Front Immunol. (2017) 8:1514. doi: 10.3389/fimmu.2017.01514
191. Peche H, Trinite B, Martinet B, Cuturi MC. Prolongation of heart allograft survival by immature dendritic cells generated from recipient type bone marrow progenitors. Am J Transplant. (2005) 5:255–67. doi: 10.1111/j.1600-6143.2004.00683.x
Keywords: tolerance, liver transplantation, operational tolerance, cell therapy, hematopoietic stem cell transplantation, regulatory T cells, regulatory dendritic cells
Citation: Du X, Chang S, Guo W, Zhang S and Chen ZK (2020) Progress in Liver Transplant Tolerance and Tolerance-Inducing Cellular Therapies. Front. Immunol. 11:1326. doi: 10.3389/fimmu.2020.01326
Received: 24 March 2020; Accepted: 26 May 2020;
Published: 24 June 2020.
Edited by:
Ye Htun Oo, University of Birmingham, United KingdomReviewed by:
Reem Al-Daccak, Institut National de la Santé et de la Recherche Médicale (INSERM), FranceFederica Casiraghi, Mario Negri Pharmacological Research Institute, Italy
Copyright © 2020 Du, Chang, Guo, Zhang and Chen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Zhonghua Klaus Chen, zc104126@126.com