Julien Subburayalu1,2,3*†- 1Department of Internal Medicine I, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany
- 2Center for Regenerative Therapies (CRTD), Technische Universität Dresden, Dresden, Germany
- 3Department of Medicine, University of Cambridge, Cambridge, United Kingdom
T follicular helper cells comprise a specialized, heterogeneous subset of immune-competent T helper cells capable of influencing B cell responses in lymphoid tissues. In physiology, for example in response to microbial challenges or vaccination, this interaction chiefly results in the production of protecting antibodies and humoral memory. In the context of kidney transplantation, however, immune surveillance provided by T follicular helper cells can take a life of its own despite matching of human leukocyte antigens and employing the latest immunosuppressive regiments. This puts kidney transplant recipients at risk of subclinical and clinical rejection episodes with a potential risk for allograft loss. In this review, the current understanding of immune surveillance provided by T follicular helper cells is briefly described in physiological responses to contrast those pathological responses observed after kidney transplantation. Sensitization of T follicular helper cells with the subsequent emergence of detectable donor-specific human leukocyte antigen antibodies, non-human leukocyte antigen antibodies their implication for kidney transplantation and lessons learnt from other transplantation “settings” with special attention to antibody-mediated rejection will be addressed.
1 Introduction
T follicular helper (TFH) cells are a specialized CD4+ TH cell population critical for driving adaptive humoral immunity (1, 2), with B-cell lymphoma 6 (Bcl6) as a repressor of B-lymphocyte-induced maturation protein 1 (Blimp-1) driving their differentiation from CD4+ T helper cells (3–5). TFH cells instruct germinal center (GC) formation which is pivotal to T cell-dependent antibody responses and their affinity maturation (6, 7). Inducible T cell co-stimulator (ICOS), C-X-C motif chemokine receptor (CXCR)5, and programmed cell death protein 1 (PD-1) are distinguishing markers of TFH cells, which contribute to lymphoid tissue homing and B cell help (8–10). The expression of C-C motif chemokine receptor (CCR)7 instructs naïve T cell migration across high endothelial venules to locate to T cell zones. Upon activation by dendritic cells, a population of activated CD4+ T cells differentiates into TFH cells through the up-regulation of Bcl6 and CXCR5 with a concomitant down-regulation of CCR7 enabling them to advance toward the C-X-C motif ligand (CXCL)13-rich B cell area in lymphoid organs (11, 12). Here, Interleukin (IL)-21 and the strength of T cell antigen receptor binding determine a long-lasting antibody response through effector antibody-secreting cells (ASCs, plasma cells) and the emergence of memory B cell subsets residing in the bone marrow termed long-lived plasma cells (LLPCs) (13–18). To date, the family of TFH cell subtypes comprises virus-specific TFH-1 cells, centrocyte-stimulating TFH-2 cells, IL-17- and IL-21-producing TFH-17 cells, and T follicular regulatory (TFR) cells (Table 1) (27). TFH-13 cells were recently identified which appear to be associated to IgE production to food and airborne allergens (64, 65). Synergies between these TFH cell subsets with B cells provide unique and necessary cues that go beyond homeostatic B cell maturation and high-affinity antibody production (66, 67).
Table 1 A snapshot on T follicular cell subtypes and some aspects of their phenotypic, transcriptional, and functional characterization.
The TFH-B cell interaction influences TFH cells to maintain a lymph node migratory phenotype (68). Besides its auxiliary effects on B cells concerning isotype switching and the formation of GCs, IL-21 appears to support TFH cells in acquiring and maintaining TFH cell gene expression in vivo in an autocrine fashion (69–71). Under physiological conditions, the emergence of high-affinity, class-switched antibodies indicates a prosperous immune response aimed at facilitating the clearance of microbial invaders or are a means to measure successful seroconversion after vaccination (72, 73). Studies have shown that improved humoral responses were preceded by an enhanced ICOS expression on circulating TFH cells (74). As such, increased ICOS+CXCR3+CXCR5+CD4+ TFH cell numbers on day 7 after antigen stimulation appear to forecast a humoral response (75). Interestingly, serological response displays Cxcr5 and IL21 induction as early as the day of the antigenic challenge (day 0), instructs antigen-specific GC responses. A failing antigen-specific TFH cell response features increased expression of IL2 and STAT5 (76). Accordingly, spatiotemporal positioning between T and B cell zones within GCs appears pivotal. For example, FoxP3hiCD4+ regulatory T (TREG) cells are predominantly confined to extrafollicular areas, whereas both TFR cells and extrafollicular TREG cells in vaccinated children are reduced following vaccination suggesting a released break in both peripheral TH cell commitment towards TFH cells (extrafollicular response) and favored cognate B cell help by TFH cells within GCs (follicular response). Besides, the release of CXCL13 into the circulation reflects the ensuing GC reactivity and correlates between TFH cells and Ag-specific B cells in tonsils (77), which can be considered an early surrogate biomarker for an ensuing humoral response (77, 78).
For humoral immunity, the functionality of TFH cells is critical and can determine successful seroconversion. For example, during acute viral infections, fate commitment of a TFH cell-to-be is acquired as early as 24 to 48 hours after infection (79). If strong interactions with antigen-presenting dendritic cells (DCs) are maintained, TFH cell differentiation is facilitated permitting TFH cell lineage determination over TH-1 cell commitment via a balanced regulation of the transcription factors Bcl6, T-box expressed in T cells (T-bet), and Blimp-1 (2, 19, 79, 80). Also, Lee et al. have reported that the downregulation of Krüppel-like Factor 2 (KLF2) further promotes the inhibition of the TFH cell differentiation-opposing transcription factors Blimp1, T-bet, and GATA binding protein (GATA)3, while the inhibition of Cxcr5 transcription is withdrawn (81). IL-10 can affect the equipoise between TH-1 cell and TFH-1 cell commitment early after antigen challenge and can enhance the degree of CD4+ and CD8+ memory T cell generation and Bcl6 expression (82).
Lately, circulating CCR7loPD-1hi TFH cell subsets were suggested to serve as surrogate markers for an ensuing humoral response (83). Moreover, a failure to down-regulate T-bet in TFH cells was shown to maintain an IFN-stimulated gene signature, which can propagate antigen persistence (28, 29). Hence, antigen persistence results in TFH-1 cell differentiation, yet may result in less meticulous B cell selection by which the origination of antigen-unspecific and self-reactive B cells and hypergammaglobulinemia is promoted (84). As a consequence, T cell exhaustion may occur (85, 86).
Lastly, the strength of T cell receptor (TCR) ligation and TCR-independent T cell activation by glycolipid recognition via CD1 contributes to determining the outcome of TFH cell-driven humoral immunity (87, 88), where weak ligation maintains T-bet to produce B cell oligoclonality, antigen persistence, TFH cell expansion, and a failing GC response.
In the context of organ transplantation, seroconversion is an undesired phenomenon since memory LLPCs residing in the bone marrow and effector ASCs within draining lymph nodes are responsible for threatening transplant longevity by imposing endothelial injury (15–18, 89). To prevent the emergence of antibodies directed against donor-specific antigenic material, donor and recipient matching for human leukocyte antigens (HLA) molecules and subjecting the recipient to an intense, life-long immunosuppression post-transplant are vital. If not adequately controlled by the immunosuppressive medication or immunodynamic interactions, the risk to develop antibody-mediated rejection (AMR) of the transplant looms. Predisposing factors for AMR include acute and chronic trauma being on hand in the transplanted setting since they disclose autoantigens, which also permit non-HLA antibodies to be patterned.
In this review, I will look back at recent and past insights into immune surveillance by TFH cells following kidney transplantation, with an emphasis on clinical data. Focus will be dedicated to the involvement of TFH cells in the emergence of autoantibodies against non-HLA autoantigens and de novo donor-specific HLA antibodies (dnDSA). Highlighting the current advances and paradigms in TFH cell biology may hold the potential to stratify transplanted patients at risk for the emergence of antibodies and may open new avenues on how to treat episodes of AMR more successfully.
2 Kidney transplantation, organ donation after circulatory death, and the detrimental impact of ischemia reperfusion injury
Previous studies have primed our understanding of factors influencing allograft tolerance. Whilst donor age and HLA mismatches were demonstrated indicators for kidney allograft survival of deceased donors, the factor age did not apply to living donations (90). Intriguingly, the presence of dnDSA more adversely affects allograft survival in donations after circulatory death (DACD) (91). Since it is obvious that deceased donor transplants are more often subject to ischemia-reperfusion injury (IRI), organ preservation and recovery may not equally be off to a favorable start when rejection episodes, the transfer of pro-inflammatory cells, and ultimately allograft survival are concerned (92). Recently, various strategies are used in animals and humans to reduce the impact of inflammatory cells on allograft longevity. In that regard, targeting immune cell diapedesis by targeting the CD62/CD62L-axis has successfully demonstrated a reduction in the adherence of pro-inflammatory immune cells to the endothelial lining (93, 94). Similarly, a cease in T cell activation via the TIM-1-TIM-4 pathway was found to foster allograft survival after IRI in mice, which conceptually can impact on their fate commitment towards further differentiation trajectories (95).
2.1 Immunosuppressive drugs influence TFH cells after kidney transplantation
Besides the transfer of pro-inflammatory cells, which is heightened in DACDs, the relevance of immunosuppressive drugs on TFH cells after kidney transplantation and transplant longevity is being increasingly appreciated, too. Although CD4+ TFH cell subpopulations reciprocally orchestrate their preeminent transcriptional regulation, immunosuppressive drugs can have a profound effect in governing subset skewing (96). Thymoglobulin induction therapy (e.g., antithymoglobulin/ATG) was reported to deplete effector CD4+ and CD8+ T cells, whilst preserving allograft permissive FoxP3+ TFR cells (97, 98). This warrants further studies investigating possible therapies that draw on TFR cell-mediated effects. This could potentially enable long-term drug-free allograft permissiveness (96, 99). This appears to be of particular importance since kidney transplant patients who have suffered from prior AMR were found to display higher ratios of IL-21+ TFH cells whilst their TFR cell population was decreased both within the graft and in the circulation. Besides, sirolimus was also found to reduce the TFR cell population even further (100). Permissiveness may also be facilitated actively by B cells since B cell depletion or IL-10 deficiency were shown to skew the tolerogenic environment towards an increased IL-21+ TFH cell population decreasing TFR cells in follicles (Figure 1) (101). By extension, basic leucine zipper ATF-like transcription factor (BATF) inhibition, a transcription factor for TH-17 and TFH-17 cells alike, could be linked to enhanced FoxP3 levels coinciding with a reduction in retinoic-acid-receptor-related orphan nuclear receptor gamma (RORγt), IL-17A, and IL-4, thus, generating tolerance after transplantation (102). Calcineurin inhibitors like cyclosporine A also impact on TFH cells. Although no effect on TFH subtypes concerning TFH-1, TFH-2, and TFH-17 cells was observed in healthy volunteers under transient cyclosporine A medication, a profound reduction in the pro-inflammatory markers IFN-γ, IL-17A, and IL-21, produced by TFH-1 and TFH-17 cells, respectively, was observed (103). This poses the question how the commonly employed permanent triple immunosuppressive therapy comprising not only of calcineurin inhibitors, but also corticosteroids and inosine-5’-monophosphate dehydrogenase (IMPDH) inhibitors, all known suppressors of T cell functionality (103–105), can lead to TFH cell dysregulation culminating in alloantibody formation and potentially allograft loss.
Figure 1 Considerations for prospective peri- and post-transplant immunosuppression. Peri- and post-transplant immunosuppressive regiments do confer differential regulatory phenotypes and need to be tailored to patient-specific demands. For example, pre-transplant administration of anti-thymocyte globulin (ATG) does deplete recipient CD4+ T helper (TH) and CD8+ cytotoxic T (TC) cells, whilst preserving the population of the recipient’s FoxP3+ regulatory T (TREG) cells. TREG cells are required to prevent the formation of de novo donor-specific human leukocyte antigen (HLA) antibodies. However, too ample TREG cell-signatures do prevent the mounting of a successful humoral immune response during microbial challenge. To understand these intricacies better, future studies are needed to elucidate the mechanisms underlying the refinement and control of TREG, TH, follicular TC, and T follicular helper (TFH) cells. To date, sirolimus and interleukin (IL)-10 deficiency were found to impair TREG cell activity. Likewise, B cell depletion (for example using rituximab) also disables TREG cell responses. Moreover, B cell depletion restores IL-21-producing TFH cell responses indirectly by alleviating the control imposed by follicular TFR cells. In contrast to sirolimus and rituximab, inhibition of basic zipper ATF-like transcription factor (BATF) does promote TREG cell responses by reducing the expression of IL-4, IL-17A, and RORγt.
Together, this argues for a better understanding of the effects of the lifelong post-transplant immunosuppressive regimen on the follicular and extrafollicular immune cell compartment to prevent sensitization to donor-specific HLA molecules or autologous non-HLA molecules with an eminent focus on the control of prevalent TFH cell responses whilst maintaining a strong TFR surveillance to induce allotolerance in kidney transplant recipients (KTxs).
2.2 Sequelae of persistent auto- and alloantigen stimulation of TFH cells
Under physiological circumstances, the evolution of a humoral memory (LLPCs) allows high-affinity antibodies to be established within a matter of days upon re-exposure of an antigen to protect us from microbial threats (106). However, auto- and alloantigenic settings constantly expose TFH cells to antigens and disturb modulating checkpoints provided by TREG cells, TFR cells, follicular cytotoxic T (TFC) cells, or even regulatory B cells. Hence, the excessive TFH cell stimulation may take a life of its own. Strategies to prevent this from happening exploit cytotoxic T-lymphocyte-associated protein 4 (CTLA-4)-specific immunoglobulin or IL-21 receptor (IL-21R) antagonists to prevent alloimmune responses (107, 108).
Hence, the surveillance of immune subtype compositions may turn out as a valuable tool in identifying KTxs at risk for the formation of auto- and alloantibodies and subsequent allograft rejection.
Considering the selective influence on TFH cells, studies on autoimmune diseases have shaped our understanding of persistent TFH cell stimulation resulting in dysregulated responses. For example, unrestricted clonal expansion of TFH cells allows the generation of ectopic lymphoid structures (ELS), which are unphysiological tertiary lymphoid follicles featuring stimulation and clonal expansion of antigen-specific B cells (109). These ELS are being established because of an antigen response yet to be cleared (110), and are formed by a regulated and well-orchestrated expression of the lymphoid chemokines C-C motif ligand (CCL)19, CCL21, and CXCL13 (111–113). Persistence of these lymphokines (with TFH cells being a major source of CXCL13) (9) allows PSGL-1LOWCD40L+ TFH-17 cells to maintain aggregates in an ICOS-dependent manner with B cells in extrafollicular ELS, inevitably preserving an immune response with a serious risk for the formation of autoantibodies of the IgG2a/IgG2b or IgG1/IgG3 type, tissue destruction, and ultimately the development of an autoantibody-mediated pathology (114–116). Autoimmune conditions and others have been shown to be associated with ELS, which are a major compartment for ample extrafollicular TFH cell accumulation (117). To date, several studies have implied TFH cells especially in the context of glomerulonephritis where IL-17 drives inflammation and autoantibody-induced kidney injury which can be considered to be key determinants for autoimmune disease activity (118–121), whilst a disrupted TFH cell response has been shown to reduction disease activity, respectively (122–124). It appears intuitive that especially endothelial injury and incessant inflammation with enhanced HLA class II up-regulation can expose autoantigens for TFH cell sensitization (125, 126). Despite the predominance of literature, particularly from human studies, on the importance of ELS for chronic inflammation caused by infections, autoimmune diseases, cancer, or transplantation (127), the contribution of derailed TFH cell activity in the induction of autoimmunity within secondary lymphoid tissues (SLOs) including the spleen, lymph nodes, and mucosal-associated lymphoid tissue (MALT) (128), may be equally important. For example, a murine study investigating the importance of TFH cells in the induction of rheumatoid arthritis found TFH cell frequencies to be significantly increased in the spleen and joint-draining lymph nodes following disease induction. Here, CXCR5-/- mice were protected from autoimmune arthritis by abrogating TFH-B cell interactions within SLOs stressing its importance in the induction of autoimmune inflammation (129). In fact, not only murine models show that immune responses in SLOs may not only precede the formation of ELS and tertiary lymphoid organs (TLOs) (130), but also maintain an active role during autoimmune conditions as is observed in patients suffering from rheumatoid arthritis, who feature follicular hyperplasia and active GC responses in SLOs (131–133).
Together, a skewed TFH cell response featuring lack of TFH-17 cell control can lead to the establishment of ELS enhancing the likelihood of TFH-17-B cell aggregates within these extrafollicular spaces for alloantibodies and alloreactive LLPCs to occur. Understanding how the disrupted TFH cell subset equipoise can be restored may hold therapeutic potential to circumvent the need for immunosuppressive therapies with its inherent adverse effects and risk for infections (134).
2.3 Donor-specific HLA antibodies and TFH cells: the feared couple to answer for antibody-mediated rejection
Although more and more details are being understood regarding characteristics of HLA epitopes to perform appropriate epitope matching in clinical settings, there remains much to be learned. To date, HLA-matching in kidney transplantation is only performed for HLA-A, -B, -C, -Bw4, -Bw6, -DR, -DR51/52/53, -DQA1, - DQB1, and -DPB1 antigens (135). Nevertheless, mismatches are mostly inevitable and enhance the risk of dnDSA formation (136). However, it appears that not every epitope is equally immunogenic. Aubert et al. have found that low-level donor-specific HLA antibodies remain controversial in terms of predicting the risk of graft failure (136, 137). Indeed, studies have proposed dnDSA directed at HLA-DQ to be a risk factor for late allograft failure that feature histological alterations in accordance with chronic AMR (138–140).
Although dnDSA appear to form at relatively low frequencies (~15%) and often only several years after transplantation, they commonly facilitate detrimental consequences (141, 142). Independent risk factors were reported to be HLA-DR mismatches and non-adherence to immunosuppressive therapy. Upon emergence, dnDSA could progress and show antibody-mediated graft injury without impaired graft function (142).
Evidence suggesting AMR to be a consequence of the presence of dnDSA effectively challenged the dogma of calcineurin inhibitor toxicity and chronic allograft nephropathy (141). In fact, capillaritis was found to forecast allograft dysfunction culminating in AMR (143–145). Not much later, Lefaucheur et al. identified four distinct patterns of kidney rejection with capillaritis in association with AMR illustrating the poorest outcomes (146). Not all dnDSA could be paired with ensuing AMR (147, 148). In that regard, dnDSA properties would matter with respect to MFI, complement-binding capacity, and IgG subclass composition (147, 149). Conversely, the clinical phenotype of AMR cannot be linked with the presence of circulating dnDSA in all cases challenging the criteria for diagnosis. In that regard, evidence comprised histological acute tissue injury, current antibody interaction with endothelium as in C4d deposition, and serological evidence of dnDSA detection or non-HLA donor-specific antibodies (150, 151). The identification of intragraft dnDSA has been proposed to enable clinicians to correctly diagnose AMR, which would not meet these criteria (151, 152). However, if serologically detectable, dnDSA presence has been attributed to a poor graft outcome imposed by AMR (139, 149, 153–155).
A clear link between AMR and TFH cells, particularly regarding IL-21 production, has been established (156). KTxs suffering from chronic allograft rejection were found to display distinctive increases in circulating TFH cells with impaired controllability given a reduced PD-1 expression (157). Accordingly, PD-1 expression fine-tunes TFH cell responses by suppressing follicular T cell recruitment, confining TFH cell localization within GCs, and increasing the stringency of GC affinity selection via suppressed phosphoinositide 3-kinase activity upon PD-L1 ligation (158). Another study found stable circulating TFH cell numbers with decreased IL-21 production. However, their ability to stimulate alloantigen-specific B cells to produce IgG was maintained (159). Stable numbers of TFH cells have also been found by Chen et al., however, indicating a skewing toward IL-21-producing TFH-17 and TFH-2 cell subpopulations in AMR (100). To control this dysregulation of TFH cells, Rodriguez-Barbosa et al. have found that whilst the CD40/L pathway could be used, the B and T lymphocyte attenuator (BTLA) pathway was dispensable (160). Exploiting the CD40/L axis revealed reduced clonal B cell expansion associated with curtailed GC-TFH cell numbers and a blunted IL-21 secretion (161). It appears that challenging cellular receptor-ligand interactions between TFH-B cells may alleviate the burden of AMR, which studies estimate to be responsible for 30-50% of allografts to fail (156). Likewise, protection from AMR could be mediated by strengthening the control of TFH cells and Ag-specific B cells by TFR cells (96, 100, 101, 155).
Therefore, TFH cells are not only capable of inducing dnDSA formation but can also further augment preexisting DSA levels following alloantigen recall (162). Conversely, TFR cells curtail TFH cell-directed B cell help by preventing dnDSA formation. Whilst lack of TFH cells control drives severe AMR, TFR cells are less involved in this process (162). These observations appear to translate to the human setting. Here, KTxs with immunogenic tolerance towards their allograft have disrupted TFH cell functionality characterized by lack of IL-21 production, although in humans TFR cells control AMR (100, 163). In a similar notion, IL-21+ TFH cells and activated B cell responses (ASCs, CD86+CD38+) together with serum IL-21 levels were proposed as biomarkers for AMR in KTxs (164, 165). A more profound understanding if certain TFH cell-related pathways predisposed to the formation of complement-fixing or non-complement fixing dnDSA, would help to develop non-invasive biomarker-guided risk stratification and molecular refinement tools to prevent the emergence of dnDSA altogether. In fact, Louis et al. recently demonstrated that TFR cells and transitional B cells were selectively reduced in KTxs with AMR (166). Characteristically, both populations comprising of CXCR5+ TFR cells and CD21- transitional B cells that had vanished expressed T-bet. Their loss coincided with enhanced inflammatory antibody responses, microvascular inflammation, and allograft failure (166). Previous studies have highlighted the importance of T-bet to act as a repressor of PD-1 and other inhibitory receptors such as LAG-3, CD160, and BTLA in adaptive immune cells (167), possibly identifying T-bet expression as a canonical immune checkpoint to drive alloreactivity in T cells (Figure 2) (168). However, it must be recognized that noncanonical pathways in the absence of TFH-B cell interactions need to be considered that may also contribute to the production of alloantibodies or certain subtypes of allospecific immunoglobulins such as IgG2c where TFH cells may be dispensable (169, 170).
Figure 2 Alloimmunity following solid organ transplantation predispose for acquiring de novo donor-specific human leukocyte antigen antibodies and antibody-mediated allograft failure. Solid organ transplants (e.g., liver or lung) are matched for human leukocyte antigens (HLA)-A, -B, and -DR before the transplantation is undertaken. After transplantation, the constant exposure to non-HLA antigens, small antigens, or (unmatched) HLA antigens predispose for the acquisition of de novo Donor-specific HLA antibodies (dnDSA), which can be detected in ~ 15% of transplanted patients years after the transplantation was performed. Risk factors for the establishment of dnDSA are mismatches for HLA-DR (HLA-DR ##) or non-adherence to taking the life-long immunosuppressive treatment. The dnDSA can be classified into non-fixing or complement-fixing antibodies. Complement fixation is associated with a pro-inflammatory response, which is the cause for transplant vasculopathy. To date, it is unclear how complement-fixing abilities of dnDSA are determined (? in box), however, HLA-DQ dnDSA were found to be a risk factor. It is speculated that T follicular helper (TFH) cell-related pathways either on the level of fate commitment upon acquisition of antigen-specificity via T cell receptor engagement or during TFH cell – B cell interactions would imprint on complement-fixing abilities of dnDSA. Irrespective of whether dnDSA can be detected in a patient, which often only attach to the transplanted vascular tissue structures of the allograft and thus evade detection by conventional blood taking methods, transplant vasculopathy drives (sub)clinical rejection episodes, which confer the risk to acquire late allograft failure. During antibody-mediated rejection (AMR) T-bet expression is lost from transitional B cells (CD21- Btrans cell) and follicular regulatory T (TFR) cells. T-bet confers instructional cues for PD-1 acquisition, thus lack of immune checkpoint modulation (ICM) can be deduced that preserves an interferon-stimulated gene signature (ISGS) upon TFH cell – B cell encounters. Perpetuation of ISGS maintains inflammation and fosters the establishment of dnDSA if immune suppressive measurements are not engaged.
Subclinical rejection episodes, a sequelae of aberrant allosensitization possibly causing loss of TFR cells, are considered prognostic indicators for chronic AMR (171, 172). Adjusting signaling pathways culminating in the absence of IL-21 production in TFH cells prevents dnDSA formation due to lack of cognate B cell help and thus fosters allotolerance (163). Hence, defying allosensitization of TFH cells, e.g., via engagement of the co-stimulatory blockade receptor CTLA-4 (100, 173), enhanced mTOR immunosuppression (174, 175), blockade of the CD40/L axis (67, 160, 161), or antagonizing antibodies against the IL-21R (108, 156, 159), may allow to further refine or counteract chronic AMR in kidney allografts. This strategy may promote longevity of kidney transplants and the quality of life in transplanted patients. Mechanisms underlying this deleterious allosensitization of naïve T cells to becoming alloreactive TFH cells are conceivable. Comparing immunosuppression with tacrolimus against co-stimulation blockade of CD80 and CD86 using the CTLA-4-Ig belatacept conferred diminished seroconversion rates to influenza vaccination (176). Hence, understanding how to prevent the selection of alloreactive TFH cell effector and memory clones will be an important area of future investigations. For example, a recent cohort study in patients with a positive dnDSA status showed an enhanced alloreactive TFH cell pool in response to donor-specific HLA antigens. Despite continuous immunosuppression compared with healthy controls, an augmented IL-21 production and proliferative response in these TFH cells upon stimulation in vitro was reported suggesting either incessantly activated or more easily recruited signaling domains even years after kidney transplantation (103). Further studies are needed to better define how to circumvent unwanted allograft-directed immune responses, whilst maintaining T cell-mediated antigen-specific B cell help in the context of the host’s immune protection and response to vaccination. GC responses emerge as prominent areas to be more meticulously studied. For example, KTxs were shown to lack GC responses to mRNA vaccination against severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2), a feature well characterized to be associated with neutralizing antibodies against SARS-CoV-2 (177). A prominent feature of this missing GC response in this study was a blunted TFH cell signature, which is considered instrumental in orchestrating architecture and functionality of GCs (6–10). One may speculate that allograft-draining lymph nodes’ GCs may present a unique architecture in patients having developed dnDSA compared to other allograft-unassociated draining lymph nodes. Recent studies have shown that the trauma of the surgical intervention requires lymphatic vessels to heal, which in murine kidney transplantation showed lymphatic endothelial cells to abundantly release CCL21 by which stromal lymph node remodeling was fostered. Accordingly, dendritic cell enrichment was observed thus increasing the chance for successful alloreactive T cell priming. The causative role of the lymphatic system pertaining to the kidney allograft could be established in retrospective analyses in humans (178). Furthermore, the formation of TLOs within the allograft itself were observed in human kidneys undergoing chronic rejection (179, 180). Besides the formation of de novo lymphatic angiogenesis, the contribution of increased lymphatic flow may be another factor by which cellular trafficking, alloimmunity, and vasculopathy are being propagated, which in the context of heart transplantation found donor cell-trafficking to allograft-draining lymph nodes, increased lymphatic vessel are, and allograft infiltration of CD4+ and CD8+ T cells as well as CD68+ macrophages (181). In fact, draining lymph nodes and TLOs after small-bowel transplant rejection were enriched in CXCR3+ host T cells stimulated by donor-derived type 1 helper T cell-related chemokines (IP-10) suggesting their possible contribution also in other solid organ transplantation contexts such as the kidney (182). Since alloreactive T cells are susceptible toward inhibition by standard immunosuppressive drugs such as corticosteroids or calcineurin inhibitors, an advanced understanding of potentially derailed signaling pathways downstream of calcineurin in cases where patients are suspected of allograft rejection despite appropriate drug levels is needed (183).
Recent studies highlight the importance to better understand cytotoxic T cell responses in GCs. Some cytotoxic T cells can acquire CXCR5 expression (28), thus enabling them to enter GCs. Compared with STAT5+CXCR5+CD8+ TFC cells, PD-1+CXCR5+CD8+ TFC cells were found to be a biomarker for AMR. In this study, PD-1+CXCR5+CD8+ T cells were associated with chronic allograft dysfunction following kidney transplantation (184). Indeed, CXCR5+ CD8+ T cells with IFN-γ-producing abilities can be sampled from the peripheral blood in higher quantities in KTxs who remain DSA-free (185). Studies in a murine system of AMR using adoptive cell transfers in CCR5 KO mice equally show reduced frequencies of CXCR5+CD8+ TFC cells following AMR of the kidney transplant (186), which confer cytotoxicity towards alloprimed IgG+ B cells. This could be a means by which incessant adaptive immune cell activation in allograft-draining lymph nodes may be held in check in transplanted patients who remain dnDSA-free.
Together, these studies implicate both TFH cell and TFR cell subsets as relevant entities to risk-stratify patients concerning potential dnDSA formation (89). Further studies are needed to better define lineage-commitment trajectories of TFC cells to comprehend how to therapeutically intervene in cases of ongoing AMR. This may hold the potential to maintain allograft longevity even in cases of severe AMR.
2.4 Non-HLA antibodies: the underestimated reason for transplant morbidity caused by exuberant sensitization of TFH cells?
Having discussed the relevance of TFH cells and their cellular modulators for the formation of HLA-specific dnDSA and the importance of TFH cell subsets for the disclosure of autoantigens and autoimmune conditions to emerge, the relevance of non-HLA antibodies remains to be outlined.
Just over a decade ago, Dragun et al. reported refractory vascular rejection in KTxs caused by non-HLA autoantibodies against the angiotensin II type 1 receptor (AT1R) (187). Similarly, transplant glomerulopathy (TG) a consequence of autoantibody formation against perlecan and agrin, both compounds of the glomerular basement membrane, was described (188). It appeared that the risk for TG was even enhanced if both dnDSA and non-HLA antibodies were coincidentally present (189). To address these descriptions, a study conducted by Amico et al. found around 2.3% of patients of their cohort, who experienced early AMR, to be due to non-HLA antibodies (190). Progressive loss of self-tolerance to the autoantigens k-α-1 tubulin, collagen type V, and the collagen I was linked to increased risk of primary graft dysfunction in lung transplantation, which in turn would augment alloimmune responses inclining towards bronchiolitis obliterans syndrome (BOS) (191, 192). The importance of activating antibodies against AT1R is by far the most thoroughly studied. AT1R and the C-terminal fragment of perlecan (LG3) were studied in pregnant transplanted women and appeared to trigger allograft rejection. The mechanism of formation did not require allosensitization and a lack of correlation suggested different mechanisms of generation (193). It was suggested that renal ischemia, alterations to the intragraft microenvironment, and alloimmunity may be some of the various factors predisposing for AT1R antibodies, which augment the ischemic condition by further contraction of the renal vasculature (187, 194, 195). The exposure of other cryptic antigens culminates in the emergence of non-HLA antibodies, which was described for the antigens LG3, vimentin, the endothelin type A receptor (ETAR), and other extracellular proteins and intermediate filaments. But also, more recently, their ability to bind to antigens present on apoptotic cells activating complement was appreciated (Figure 3) (195–198).
Figure 3 Transplant glomerulopathy in the context of non-human leukocyte antigen antibodies. Constant cellular turnover as occurs through programmed-cell death or damage to the transplanted organ predisposes for the disclosure of autoantigens. To date, the C-terminal fragment of perlecan (LG3), agrin, vimentin, the angiotensin II type 1 receptor (AT1R), the endothelin type A receptor (ETAR), k-α-1 tubulin, collagen type V, and collagen type I have been identified as serving as autoantigens with risk for progressive loss of self-tolerance. This loss of self-tolerance can result in their presentation by tissue-resident phagocytes and serological acquisition of non-human leukocyte antigen (non-HLA) antibodies without prior allosensitization. Interestingly, LG3 and agrin are composite material of the glomerular basement membrane (GBM) and can thus drive transplant glomerulopathy (TG) via renal vascular constriction, which was studies in pregnant kidney transplanted women. In this study by Hönger et al. AT1R was also identified to mediate TG. TG can cause early antibody-mediated rejection (AMR) and it was found that ~ 2.3% of these cases are due to non-HLA antibodies. Risk factors that mediate this process comprise ischemia-reperfusion injury (IRI), intragraft microenvironment alterations, or alloimmunity, which drives the up-regulation of major histocompatibility complex (MHC) class II (MHCII) on antigen-presenting cells, thereby upping the odds of successful cross-presentation to T helper cells. Studies have found that non-HLA antibodes can activate complement. Moreover, their pathology also entails FC-receptor-independent effects. For example, they can induce neointima formation, enhance the accumulation of smooth muscle cells, and promote vascular remodeling.
Evidence also suggests FC-independent effects of non-HLA antibodies like augmented neointima formation with an accumulation of smooth muscle cells, mesenchymal stem cells advocating for their regulatory function via ERK1/2 signaling and interactions with α2β1 integrins in obliterative vascular remodeling during rejection (199, 200). But also other conditions have seen the discovery of non-HLA autoantibodies including systemic sclerosis with or without associated pulmonary arterial hypertension (201, 202).
It was shown that apoptotic cells release exosome-like vesicles, which, mediated by the 20S proteasome, incite non-HLA antibody formation. This coincided with enhanced TFH and GC B cells (203). The conceptual framework of apoptosis taking place constantly may allow us to explain why some non-HLA autoantibodies may be present pre-transplant. In fact, a study by Nagele et al. reported ample naturally occurring immunoglobulin (Ig) G autoantibodies, which were influenced by age, gender, and disease (204).
Together, copious amounts of studies highlight the importance of auto- and allosensitization of TFH cells in generating a permissive environment to stimulate cognate Ag-specific B cells toward the production of both non-HLA autoantibodies and dnDSA. Therefore, clinicians need to carefully monitor patients to identify derailed homeostatic interactions even in the absence of measurable auto- or allosensitization (205). It is noteworthy that compartments reflecting dysbalanced interactions (ELS, allograft draining lymph nodes) are not part of the regular clinical routine suggesting that further research is needed to define appropriate biomarkers that may reflect the current state of health of these compartments. Moreover, a more fundamental understanding about how these antibodies evolve from a TFH cell perspective may identify interventions potent to either decrease the intensity of the antibodies detected or even reverse their presence after all.
3 Lessons learnt on TFH cells from other solid organ transplantation settings
Besides kidney transplantation, TFH cell biology has also been studied in the context of other solid organ transplantations (Table 2). Although organ-specific biology considering epigenetic, molecular, cellular, and environmental effects cannot be ruled out in T cell biology, these findings can instruct experimental nephrologist to consider similar trends in kidney transplantation (215–217).
Table 2 A summary on the reported impact of T follicular cell subtypes in the context of solid organ transplantation settings.
Towards the turn of the millennium, MHC class I, mainly HLA-A, antibodies had been described to forecast the development of BOS (210, 218). Other reports reliably confirmed their detrimental impact on lung allograft longevity as they caused persistent-recurrent lung rejections and chronic allograft dysfunctions (219, 220). Moreover, dnDSA were found to occur more frequently as is the case in other solid organ transplantation settings (148). Despite their frequency, their full impact remains yet to be fully elucidated with intragraft dnDSA noticed to carry a higher risk for lung allograft loss (148). Formation of dnDSA after lung transplantation corresponds to a high risk of refractory acute cellular rejection, lymphocytic bronchiolitis (with an increased influx of lymphocytes and neutrophils in bronchoalveolar lavages) (221), and BOS (222). Lately, Krupnick et al. have described the importance of CD8+CD44hiCD62LhiCCR7+ TREG cells in a mouse lung transplant model, which patrolled the lung successfully to endorse allotolerance (223). Furthermore, Li et al. have recently demonstrated that depletion of CD4+CD45.2+FoxP3+ TREG cells induced the emergence of dnDSA resulting in AMR (155). According to the authors, TREG cell depletion allowed CXCL13-mediated graft infiltration of CD4+Bcl6+CXCR5+PD-1+ TFH cells and IgM dnDSA to be patterned. Ultimately, complement would deposit and destroy the airway epithelium, a process which could be reversed by CXCL13 blockade or utilization of CD40/L and ICOS/L pathway inhibition (Figure 4) (155). This suggests that even severe endothelial cell injury could be reversed if the right immunological setscrew was identified. These findings warrant similar research in the context of kidney transplantation. Bypassing both TFH cell or TREG cell influence on lung allograft longevity, a study has also successfully described B cell-targeted inhibition impeding follicle formation and eventually preventing BOS after lung transplantation (224).
Figure 4 Strategies to foster transplant longevity for donations after circulatory death. Donations after circulatory death (DACD) comprise the largest fraction of organs available for transplantation. However, due to reduced circulation ischemia-reperfusion injury (IRI) has often occurred, which may be even exacerbated depending on factors including age, sex, or mismatches in the human leukocyte antigen (HLA) system. This disadvantages the length of organ preservation possible and potential chances for recovery upon transplantation. Moreover, the IRI does confer migratory effects to donor pro-inflammatory cells like polymorphonuclear neutrophils (PMNs) or IL-17A-producing T helper (TH17) cells, which are being transplanted jointly with the organ. However, to prevent incessant recipient pro-inflammatory immune cell recruitment towards the inflamed organ, several strategies are being explored evolving around the issue of disabling immune cell diapedesis. For example, the CD62-CD62L axis or the TIM-1-TIM-4 pathway can be targeted since CD8+CD44hiCD62LhiCCR7+ TREG cells patrol the lung to endorse alloimmunity after lung transplantation. Pending successful implementation, transplant longevity may also conceptually be fostered by employing co-stimulation inhibitory approaches for the CD40/CD40L-axis, the ICOS/ICOSL-pathway, or by CXCL13 blockade to deplete donor-specific memory T cells. Following an infection that drives interferon (IFN)-γ expression, donor-specific memory T cell populations can expand and contribute to an IgM alloantibody response in a CD40-independent manner. As above, these IgM alloantibodies activate compliment and drive microvasculature inflammation that up the odds for late allograft failure.
In heart transplantation (HTx), the importance of alloreactive memory TFH cells has been delineated previously. In that regard, memory TFH cells were shown to be the barrier to long-term allograft survival as they support antibody isotype switching and alloreactive effector TFH cell damage (206). Moreover, inhibiting memory CD4 TH cell trafficking was assessed by Zhang et al. and effectively described to prolong HTx survival in sensitized patients with alloreactive memory TFH cells, a cohort that is particularly prone to insufficient co-stimulation blockade (206, 207). By employing lymphoid sequestration, TREG cell differentiation was advocated (225). More recently, Gorbacheva et al. have found that CD40-independent alloantibody responses were facilitated by IFN-γ producing TH cells and may be the cause for deleterious alloantibody responses despite co-stimulation blockade (208). Especially TH-1 and TH-17 cells promoted dnDSA responses (208, 209), while also displaying CD40-independent help to alloreactive effector CD8+ T cells (209). Together, this suggests that follicular and extrafollicular alloreactive B cell responses need to be screened in experimental models to identify pathways by which this extrafollicular CD40-independent B cell help can be curtailed and rather host protective and allograft-permissive T cell biology can be regained.
In liver transplantation (LTx), cytokines related to TFH-1 and TFH-17 cells, IFN-γ and IL-17, have been identified to risk stratify patients regarding their risk of rejection (211, 212). More recently, TFH cell dynamics were studied by Zhang et al. one day before up to one-month post-transplant. In their study, the authors have shown an unchanged TFH cell frequency in the circulation, however, a reduced production of IL-21 one month after LTx was noticed. Despite the lack in IL-21 production, these TFH cell could provide cognate B cell help with unaltered production of immunoglobulins in ex vivo cultures (213).
Lastly, pancreas transplantation utilizes similar draining lymph nodes of the paracaval and paraaortic affiliation. There are essentially three forms of pancreas transplantations (PTx) currently in practice: simultaneous pancreas-kidney (SPK), isolated pancreas (IP), and islet cell transplantation. As with other forms of organ transplantation, the deleterious impact of alloreactive TFH cells was also investigated regarding tissue reactivity and alloantibody production. In a study conducted by Vendrame et al., tissue-reactive TH cells were described to precede insulinitis, β-cell loss, and hyperglycemia due to C-peptide loss mediated by the emergence of autoantibodies (214). These negative consequences could be attenuated by non-specific T cell depletion (214). The challenge that alloreactive TH cell pose to transplantation was delineated by another group (226). They described the serious adverse effects imposed on PTx survival by the emergence of dnDSA where, on average, 14.7% developed dnDSA, which was more frequent in IP (~ 19%) and showed an inferior outcome compared to non-donor HLA. This renders the detection of dnDSA as a strong independent predictor of pancreas allograft failure (226). Another independent study also reported in ~ 15.6% the appearance of dnDSA, predominantly class II-specific, whereas non-DSA were mostly of class I-specific nature (227). More recently, it was described that dnDSA would occur equally likely in PTx and islet cell transplantation, also being mostly class II-specific (228). Finally, more frequent, and severe rejection episodes were linked to the presence of dnDSA rather than non-DSA or antibody-negative patients (227).
4 Conclusions
TFH cells play a crucial role in the host’s immune response and allow humoral memory to be established and maintained. However, when sensitized, particularly in a setting of persistent antigen presentation, TFH cell responses are not well studied and may be surprising. Here, their responses may stretch from inabilities to mount an appropriate antibody response thus resulting in an inability to clear microbial threats or even overwhelming immune responses despite immunosuppression. The latter carries the risk of seroconversion of alloantibodies that can cause AMR. We have a lot to learn about TFH cells, their interaction with B cells, TREG cells, TFR cells, regulatory B cells, or tissue-resident (or recruited) myeloid cells including macrophages, dendritic cells, and neutrophils. Advances in drug availability may cause a skewing of subpopulations, which may constitute an advantage or disadvantage given the respective immunological context. Taken together, progress in TFH cells’ biology and unveiling their relation to CXCR5+CD8+ TFC cell subsets or TFR cells may hold the potential not only to risk stratify transplanted patients but moreover to regain control in cases of severe allograft injury and to reinforce allotolerance. This may bring about significant changes how we detect and treat AMR in KTxs. It is conceivable that based on an enhanced immunological understanding, AMR treatment by intensifying the immunosuppressive regimen to become a matter of the past. We should be confident that further studies can significantly improve transplant longevity, and ultimately the quality of life of transplanted patients.
Author contributions
The author confirms being the sole contributor of this work and has approved it for publication.
Funding
JS was funded by a scholarship from the German Academic Scholarship Foundation (Studienstiftung des deutschen Volkes) and by the German Research Foundation (DFG, Clinician Scientist position, SU 1360/1-1).
Acknowledgments
The author thanks Ricardo Lira Martinez for feedback on the manuscript. The Article Processing Charge (APC) were funded by the joint publication funds of the TU Dresden, including Carl Gustav Carus Faculty of Medicine, and the SLUB Dresden as well as the Open Access Publication Funding of the DFG.
Conflict of interest
The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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Glossary
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Keywords: HLA antigens, T follicular helper cell, transplantation immunology, solid organ transplantation, kidney transplantation, donor-specific HLA antibody, non-HLA antibody, antibody-mediated rejection
Citation: Subburayalu J (2023) Immune surveillance and humoral immune responses in kidney transplantation – A look back at T follicular helper cells. Front. Immunol. 14:1114842. doi: 10.3389/fimmu.2023.1114842
Received: 02 December 2022; Accepted: 22 June 2023;
Published: 12 July 2023.
Edited by:
Helong Dai, Central South University, ChinaReviewed by:
Yoshiko Matsuda, National Center for Child Health and Development (NCCHD), JapanGowthaman Uthaman, University of Massachusetts Medical School, United States
Copyright © 2023 Subburayalu. 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: Julien Subburayalu, julien.subburayalu@tu-dresden.de
†ORCID: Julien Subburayalu, orcid.org/0000-0001-9243-0558