Paola Vacca1*†
Elisa Montaldo2†
Daniele Croxatto1
Francesca Moretta3,4
Alice Bertaina5
Chiara Vitale1,6
Franco Locatelli5,7
Maria Cristina Mingari1,6,8Lorenzo Moretta9*
- 1Department of Experimental Medicine, University of Genova, Genova, Italy
- 2Division of Regenerative Medicine, Stem Cells and Gene Therapy, San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milano, Italy
- 3Department of Internal Medicine, University of Verona, Verona, Italy
- 4Ospedale Sacro Cuore Negrar, Verona, Italy
- 5Department of Pediatric Hematology and Oncology, IRCCS Bambino Gesù Children’s Hospital, Rome, Italy
- 6U.O. Immunology IRCCS AOU San Martino-IST, Genova, Italy
- 7Department of Pediatrics, University of Pavia, Pavia, Italy
- 8Centro di Eccellenza per la Ricerca Biomedica – CEBR, Genova, Italy
- 9Department of Immunology, IRCCS Bambino Gesù Children’s Hospital, Rome, Italy
Natural killer (NK) cells play a major role in the T-cell depleted haploidentical hematopoietic stem cell transplantation (haplo-HSCT) to cure high-risk leukemias. NK cells belong to the expanding family of innate lymphoid cells (ILCs). At variance with NK cells, the other ILC populations (ILC1/2/3) are non-cytolytic, while they secrete different patterns of cytokines. ILCs provide host defenses against viruses, bacteria, and parasites, drive lymphoid organogenesis, and contribute to tissue remodeling. In haplo-HSCT patients, the extensive T-cell depletion is required to prevent graft-versus-host disease (GvHD) but increases risks of developing a wide range of life-threatening infections. However, these patients may rely on innate defenses that are reconstituted more rapidly than the adaptive ones. In this context, ILCs may represent important players in the early phases following transplantation. They may contribute to tissue homeostasis/remodeling and lymphoid tissue reconstitution. While the reconstitution of NK cell repertoire and its role in haplo-HSCT have been largely investigated, little information is available on ILCs. Of note, CD34+ cells isolated from different sources of HSC may differentiate in vitro toward various ILC subsets. Moreover, cytokines released from leukemia blasts (e.g., IL-1β) may alter the proportions of NK cells and ILC3, suggesting the possibility that leukemia may skew the ILC repertoire. Further studies are required to define the timing of ILC development and their potential protective role after HSCT.
Introduction
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) still represents a major therapeutic option for severe hematological and immunological disorders (1). However, success of allo-HSCT can be impaired by graft-versus-host disease (GvHD) and, in the case of high-risk hematological malignancies, also by disease relapse. The clinical outcome can also be hampered by infections favored by the delayed immune reconstitution in transplanted patients (1). Moreover, only 60% of patients may find a related or unrelated HLA-matched donor. For the remaining patients, umbilical cord blood (UCB) may represent an alternative source of HSC (2). UCB transplant allows a less stringent HLA-matching between donor and recipient, but it is frequently associated with delayed neutrophil engraftment and delayed T-cell reconstitution. Moreover, UCB transplant recipient cannot benefit from the adoptive transfer of antigen-experienced donor T-cells (2). Another important therapeutic option is represented by the haploidentical (haplo)-HSCT. In this setting, the donor (in most instances, a parent) is identical for one HLA haplotype and mismatched for the other one (3). Given the high degree of HLA disparity, haplo-HSCT requires an extensive T-cell depletion of the graft (3) or heavily posttransplantation immune-suppressive therapy to prevent severe GvHD (4). In both UCB-HSCT and haplo-HSCT settings, the immune-compromised hosts are highly susceptible to a wide range of opportunistic infections. Thus, cells of the innate immunity are the only players exerting a major defensive role for several months before the restoring of adaptive immune responses. In particular, natural killer (NK) cells can provide protection against viral reactivation and/or primary infections. Perhaps, more importantly, the presence of alloreactive NK cells provides a potent graft-versus-leukemia (GvL) effect that contributes to tumor eradication (4, 5). It is now clear that NK cells are one of the components of a broad family of innate lymphoid cells (ILCs). However, so far, little is known on the possible role of the other ILC subsets in haplo-HSCT. Here, we will summarize our current knowledge on ILCs both in murine models and in human studies, since they could result crucial in host defenses after HSCT.
ILC Subsets
Different from T-cells and B-cells, ILCs are a group of lymphocytes that do not express rearranged antigen-specific receptors (6). ILCs represent a heterogeneous family of cells classified on the basis of their transcriptional and functional profile. Similar to T-cells, ILCs have been grouped into cytotoxic-ILC and helper-ILC (6). NK cells represent the cytotoxic-ILC population (7). They express eomesodermin (Eomes) and T-box transcription factor (T-bet), display cytolytic activity, and produce pro-inflammatory cytokines, primarily IFNγ and TNF. Helper-ILC population is further subdivided into three groups, namely: ILC1, ILC2, and ILC3 (6). ILC1 depend on the expression of the T-bet transcription factor for their development and secrete IFNγ, but, different from NK cells, they neither express Eomes nor exert cytolytic activity (7). ILC2 express GATA-binding protein 3 (GATA3) and produce type-2 cytokines, including IL-13 and IL-5 (8). Finally, ILC3 are a heterogeneous cell population, including fetal lymphoid tissue-inducer (LTi) cells and adult ILC3 that are further subdivided into natural cytotoxicity receptors− (NCR−) and NCR+ subsets. Collectively, ILC3 are defined by the expression of the retinoic acid receptor-related orphan receptor (RORγt) and produce mainly IL-17 and IL-22 (9). Studies in mice revealed that ILC, similar to T-cells and B-cells, derive from the common lymphoid progenitors (CLPs). The expression of the Id2 transcription factor determines further commitment toward a precursor common to all ILC subsets. While the NK cell precursor diverges early from the other ILC lineages, all helper-ILCs share a common helper-ILC progenitor (CHILP). Subsequently, upon exposure to different cytokines and/or to environmental cues, the CHILP differentiate toward ILC1, ILC2, or ILC3 (9). In humans, the developmental pathways are less characterized (10). However, NK and ILC3-committed precursors have recently been identified. Indeed, Renoux and coworkers identified, in several fetal and adult tissues, Lin−CD34+CD38+CD123−CD45RA+CD7+CD10+CD127− cells able to differentiate exclusively toward cytotoxic NK cells both in vitro and in vivo (11). The ILC3 precursors, identified according to the Lin−CD34+RORγt+ phenotype, have been detected selectively in tonsils and intestinal lamina propria (12).
ILC in Host Defenses against Pathogens and in Tissue Remodeling
In view of the heterogeneous cytokine profile and function of different ILC subsets, it is conceivable that ILCs may contribute to host defenses against a broad variety of pathogens (13, 14). Our knowledge on human ILC1 and their functional profile are still rather limited (15–17). Taking advantage of murine models, it has been shown that ILC1, thanks to the production of IFN-γ and TNF, contribute to immune responses against intracellular pathogens, such as Toxoplasma gondii (18). Also, NK cells are an important source of IFN-γ and TNF and, in addition, display very important effector functions, such as natural cytotoxicity and antibody-dependent cell-mediated cytotoxicity (ADCC). In the context of antimicrobial defenses, NK cells are primarily involved in the control of different viral infections, primarily herpes-viruses, but may also exert a protective role against bacterial and parasitic infections (19, 20). Of note, NK cells, thanks to their potent cytolytic activity, play also an important role against tumors (Figure 1) (21).
Figure 1. ILC subsets and function. Graphic representation of the role played by ILC subsets in host defenses and tissue homeostasis/repair.
Host protection against parasites requires type-2 responses. A number of findings indicate that, during helminthic infections, epithelial cell-derived IL-25, IL-33, and thymic stromal lymphopoietin (TSLP) induce IL-13 release from ILC2 (22–24). In turn, IL-13 increases mucus production and smooth muscle contractility, thus contributing to the control of parasitic infections (25). In addition, dendritic cell (DC)-derived IL-23 and IL-1β cytokines induce the release of IL-22 and IL-17 by ILC3 (26–29). In turn, these ILC3-derived cytokines promote the production of antimicrobial molecules and neutrophil recruitment, enhancing the response against extracellular bacteria and fungi (14, 27, 30, 31) (Figure 1). In humans, the role played by ILC2 and ILC3 in defenses against pathogens is still undefined (10). Notably, patients experiencing helminthic infections show increases in ILC2 proportions; however, the role of ILC2 in anti-parasitic responses needs further investigation to be precisely clarified (8). Besides their antimicrobial function, ILCs are also involved in processes of tissues remodeling/repair. In particular, ILC2 appear to be involved in resolution of damages caused by viral or parasitic infections in lung tissues. Indeed, in response to IL-33, ILC2 also produce amphiregulin that promotes airway epithelial cell repair (32). Fetal LTi cells were the first ILC3 population to be described. LTi cells coordinate lymphoid organogenesis through their interaction with stromal cells by means of the LTαβ/LTβ receptor, leading to the upregulation of ICAM-1 and VCAM adhesion molecules on stromal cells (33). More recently, postnatal ILC3 have been shown to promote both survival and proliferation of stromal cells, following lymphoid tissue damage caused by viral infection and/or irradiation (34) (Figure 1). In addition, ILC3-derived IL-22 exerts a protective role on intestinal epithelial stem cells, particularly in the context of tissue damage caused by irradiation and/or acute GvHD (35, 36).
ILC and HSCT
So far, only a limited number of studies addressed the role of helper-ILC in the context of HSCT (35–37).
Reconstitution
Chemotherapy and radiotherapy treatment before HSCT induces extensive tissue damages in the host, including severe intestinal mucositis (38). Such damages can be even worse after allo-HSCT, if donor T lymphocytes attack the recipient intestinal epithelium (GvH reaction) (39). In a murine model of acute GvHD, Hanash and coworkers showed that host-derived IL-22 could substantially limit the development of GvHD (35). They could identify intestinal ILC3 subset as a main producers of IL-22 after total body irradiation treatment. In particular, IL-22 seemed to play a crucial role in the protection against epithelial cell damage and in preserving intestinal stem cells. These data are further supported by the finding that treatment with IL-22, in mice receiving bone marrow transplantation, resulted in increased intestinal stem cell recovery, in enhanced epithelial cell regeneration, and in reduction of intestinal GvHD (36). Given the role of ILC3 in lymphoid organogenesis and in lymphoid tissue remodeling, a role for these cells could also be envisaged in the regeneration of lymphoid tissues damaged by radiations (38, 40). Of note, ILC3-derived IL-22 can also favor the recovery of thymic epithelial cells, thus allowing a more efficient and rapid reconstitution of T-cell compartment (Table 1) (41). Conversely, it remains to be determined whether ILC3 also contribute to the regeneration of secondary lymphoid organs. In this context, it is recently shown that gamma irradiation used in conditioning regimen before HSCT may exert a long-lasting effect on secondary lymphoid organ structure and function (40). Also, ILC2 appear to be involved in epithelial tissue repair, particularly in lung tissues; however, no data are available to support an actual protection exerted by these cells in GvHD-induced tissue damages (42).
Table 1. This table summarizes the main function exerted by distinct ILC subsets and the possible role exerted by these cells in the context of HSCT.
Graft-versus-Host Disease
In the context of human HSCT, only a single study investigated the possible role of ILCs in the protection from GvHD. It was suggested that both host and donor ILCs might exert a protective role (37). The expression of activation markers and of gut and skin homing receptors on host ILCs, detected prior to HSCT, correlated with a lower incidence of both mucositis and GvHD. Notably, after HSCT, ILCs detectable in peripheral blood (PB) are of donor origin. An early appearance of activated NCR+ILC3 correlated with reduced risk of developing GvHD. In light of these finding, it is conceivable that the induction of a rapid ILC3 expansion/generation after HSCT may protect from GvHD. In this context, we have recently shown that granulocyte-colony-stimulating factor (G-CSF) could affect ILC3 and NK cell differentiation (43). Of note, G-CSF is used in UCB transplantation to accelerate engraftment and neutrophil recovery and is also used as a potent HSC mobilizing agent, before collection of HSC from donor PB (2, 44). Accordingly, we observed that HSC recovered after G-CSF-induced mobilization display a delayed and lower ILC3 and NK cell differentiation in vitro as compared to HSC isolated from bone marrow or UCB (43). These findings suggest that pre- and posttransplant treatment with G-CSF may affect ILC3 generation. Further studies should confirm these results in vivo and establish possible correlations with the occurrence of GvHD. Of note, it has been shown that ILC development may be impaired in patients with acute myeloid leukemia (AML) (45). Thus, after HSCT, ILC development might be affected by the presence of high residual leukemia burden or leukemia relapse. Indeed, it has been shown that HSC, when cultured in the presence of IL-1β-releasing AML blasts, display an impaired ability to differentiate toward ILC3 (46). Although in these culture setting the generation of NK cells seemed to be favored over ILC3, the final number of NK cells recovered was dramatically lower than those recovered in control cultures. Thus, if this inhibitory effect occurs also in vivo, it could have a negative impact on the NK-mediated GvL in haplo-HSCT. Of note, NK cell generation and differentiation after HSCT may be affected by immune-suppressor drugs, such as calcineurin inhibitors, used for treatment of GvHD (47, 48). On the other hand, helper-ILC reconstitution does not seem to be affected by cyclosporine or corticosteroids (37).
Opportunistic Infections
Studies in mice revealed that ILC might contribute to host defenses against different pathogens. In particular, while they are crucial in the control of infections in immune-compromised mice (18, 28, 49, 50), their actual role in the presence of a functional T-cell compartment seems to be marginal [as in the case of ILC3 during Citrobacter rodentium infection (51)]. However, as discussed above, patients transplanted with UCB cells or recipients of T-cell depleted haploidentical allograft experience a delayed recovery of both T-cell and B-cell adaptive responses, thus suggesting a possible relevant role of ILC in these transplantation settings. Accordingly, a rapid ILC differentiation after HSCT could guarantee an efficient host defense against opportunistic infections. Whether ILC1, ILC2, and ILC3 may indeed play a role in the control of infections in immune-compromised host, such as HSCT patients, has not been addressed yet. In contrast, clear evidence exists that patients with NK cell deficiencies and patients with functional NK cell defects display a higher susceptibility to viral infections [reviewed in Ref. (52)]. Moreover, in humanized mouse models, NK cells are required to effectively control Epstein–Barr virus (EBV) reactivation even in the presence of CD8+ T-cells (53). NK cells also contribute to host protection against cytomegalovirus (CMV) (20, 54) also in the context of HSCT (55). In particular, NK cell involvement in CMV control is suggested by the finding that certain KIR haplotypes correlate with decreased CMV reactivation after transplantation (56). On the other hand, CMV, similar to other viral infections, can dramatically shape the NK cell repertoire (57–68). In humans, CMV infection is accompanied by a rapid NK cell maturation, the acquisition of KIR and CD57, and a selective expansion of a NKG2C+ NK subset (62, 63, 67).
Concluding Remarks
Information available on ILC development and function derives primarily from studies performed in mice. Although these studies could provide reliable models of ILC differentiation, further analyses are required to address the dynamics of helper-ILC reconstitution after HSCT, the influence of HSC source, and the possible interference of cytokines produced by leukemia cells with ILC development. In addition, it will be crucial to clarify the role of specific ILC subsets in response to infections. Key information is still lacking in humans, not only on the role of ILC during infections but also in lymphoid tissue homeostasis. The possible exploitation of ILC in the context of HSCT requires a deeper knowledge of the mechanisms regulating their function and of the stimuli that drive their development.
Author Contributions
All the authors provided data reported in this review. PV, EM, CV, and LM wrote and revised the manuscript.
Conflict of Interest Statement
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.
Funding
This work was supported by AIRC: IG2010 project n.10225 (LM), IG2014 project n.15283 (LM), and “Special Program Molecular Clinical Oncology 5 × 1000” project n.9962 (LM and FL). Ministero della Salute: RO strategici 8/07 (MM) and PRIN [(Progetti di Rilevante Interesse Nazionale), FL].
References
1. Copelan EA. Hematopoietic stem-cell transplantation. N Engl J Med (2006) 354:1813–26. doi:10.1056/NEJMra052638
2. Danby R, Rocha V. Improving engraftment and immune reconstitution in umbilical cord blood transplantation. Front Immunol (2014) 5:68. doi:10.3389/fimmu.2014.00068
3. Locatelli F, Pende D, Mingari MC, Bertaina A, Falco M, Moretta A, et al. Cellular and molecular basis of haploidentical hematopoietic stem cell transplantation in the successful treatment of high-risk leukemias: role of alloreactive NK cells. Front Immunol (2013) 4:15. doi:10.3389/fimmu.2013.00015
4. Ruggeri L, Capanni M, Urbani E, Perruccio K, Shlomchik WD, Tosti A, et al. Effectiveness of donor natural killer cell alloreactivity in mismatched hematopoietic transplants. Science (2002) 295:2097–100. doi:10.1126/science.1068440
5. Moretta L, Locatelli F, Pende D, Marcenaro E, Mingari MC, Moretta A. Killer Ig-like receptor-mediated control of natural killer cell alloreactivity in haploidentical hematopoietic stem cell transplantation. Blood (2011) 117:764–71. doi:10.1182/blood-2010-08-264085
6. Diefenbach A, Colonna M, Koyasu S. Development, differentiation, and diversity of innate lymphoid cells. Immunity (2014) 41:354–65. doi:10.1016/j.immuni.2014.09.005
7. Seillet C, Belz GT, Huntington ND. Development, homeostasis, and heterogeneity of NK cells and ILC1. Curr Top Microbiol Immunol (2015) 395:37–61. doi:10.1007/82_2015_474
8. Halim TY. Group 2 innate lymphoid cells in disease. Int Immunol (2016) 28:13–22. doi:10.1093/intimm/dxv050
9. Montaldo E, Juelke K, Romagnani C. Group 3 innate lymphoid cells (ILC3s): origin, differentiation, and plasticity in humans and mice. Eur J Immunol (2015) 45:2171–82. doi:10.1002/eji.201545598
10. Montaldo E, Vacca P, Vitale C, Moretta F, Locatelli F, Mingari MC, et al. Human innate lymphoid cells. Immunol Lett (2016). doi:10.1016/j.imlet.2016.01.007
11. Renoux VM, Zriwil A, Peitzsch C, Michaelsson J, Friberg D, Soneji S, et al. Identification of a human natural killer cell lineage-restricted progenitor in fetal and adult tissues. Immunity (2015) 43:394–407. doi:10.1016/j.immuni.2015.07.011
12. Montaldo E, Teixeira-Alves LG, Glatzer T, Durek P, Stervbo U, Hamann W, et al. Human RORgammat(+)CD34(+) cells are lineage-specified progenitors of group 3 RORgammat(+) innate lymphoid cells. Immunity (2014) 41:988–1000. doi:10.1016/j.immuni.2014.11.010
13. McKenzie AN, Spits H, Eberl G. Innate lymphoid cells in inflammation and immunity. Immunity (2014) 41:366–74. doi:10.1016/j.immuni.2014.09.006
14. Sonnenberg GF, Artis D. Innate lymphoid cells in the initiation, regulation and resolution of inflammation. Nat Med (2015) 21:698–708. doi:10.1038/nm.3892
15. Bernink JH, Peters CP, Munneke M, te Velde AA, Meijer SL, Weijer K, et al. Human type 1 innate lymphoid cells accumulate in inflamed mucosal tissues. Nat Immunol (2013) 14:221–9. doi:10.1038/ni.2534
16. Fuchs A, Vermi W, Lee JS, Lonardi S, Gilfillan S, Newberry RD, et al. Intraepithelial type 1 innate lymphoid cells are a unique subset of IL-12- and IL-15-responsive IFN-gamma-producing cells. Immunity (2013) 38:769–81. doi:10.1016/j.immuni.2013.02.010
17. Vacca P, Montaldo E, Croxatto D, Loiacono F, Canegallo F, Venturini PL, et al. Identification of diverse innate lymphoid cells in human decidua. Mucosal Immunol (2015) 8:254–64. doi:10.1038/mi.2014.63
18. Klose CS, Flach M, Mohle L, Rogell L, Hoyler T, Ebert K, et al. Differentiation of type 1 ILCs from a common progenitor to all helper-like innate lymphoid cell lineages. Cell (2014) 157:340–56. doi:10.1016/j.cell.2014.03.030
19. Horowitz A, Stegmann KA, Riley EM. Activation of natural killer cells during microbial infections. Front Immunol (2012) 2:88. doi:10.3389/fimmu.2011.00088
20. Lanier LL. Evolutionary struggles between NK cells and viruses. Nat Rev Immunol (2008) 8:259–68. doi:10.1038/nri2276
21. Moretta L, Pietra G, Montaldo E, Vacca P, Pende D, Falco M, et al. Human NK cells: from surface receptors to the therapy of leukemias and solid tumors. Front Immunol (2014) 5:87. doi:10.3389/fimmu.2014.00087
22. Moro K, Yamada T, Tanabe M, Takeuchi T, Ikawa T, Kawamoto H, et al. Innate production of T(H)2 cytokines by adipose tissue-associated c-Kit(+)Sca-1(+) lymphoid cells. Nature (2010) 463:540–4. doi:10.1038/nature08636
23. Neill DR, Wong SH, Bellosi A, Flynn RJ, Daly M, Langford TK, et al. Nuocytes represent a new innate effector leukocyte that mediates type-2 immunity. Nature (2010) 464:1367–70. doi:10.1038/nature08900
24. Price AE, Liang HE, Sullivan BM, Reinhardt RL, Eisley CJ, Erle DJ, et al. Systemically dispersed innate IL-13-expressing cells in type 2 immunity. Proc Natl Acad Sci U S A (2010) 107:11489–94. doi:10.1073/pnas.1003988107
25. Maizels RM, Hewitson JP, Smith KA. Susceptibility and immunity to helminth parasites. Curr Opin Immunol (2012) 24:459–66. doi:10.1016/j.coi.2012.06.003
26. Cella M, Fuchs A, Vermi W, Facchetti F, Otero K, Lennerz JK, et al. A human natural killer cell subset provides an innate source of IL-22 for mucosal immunity. Nature (2009) 457:722–5. doi:10.1038/nature07537
27. Gladiator A, Wangler N, Trautwein-Weidner K, LeibundGut-Landmann S. Cutting edge: IL-17-secreting innate lymphoid cells are essential for host defense against fungal infection. J Immunol (2013) 190:521–5. doi:10.4049/jimmunol.1202924
28. Satoh-Takayama N, Vosshenrich CA, Lesjean-Pottier S, Sawa S, Lochner M, Rattis F, et al. Microbial flora drives interleukin 22 production in intestinal NKp46+ cells that provide innate mucosal immune defense. Immunity (2008) 29:958–70. doi:10.1016/j.immuni.2008.11.001
29. Sonnenberg GF, Monticelli LA, Elloso MM, Fouser LA, Artis D. CD4(+) lymphoid tissue-inducer cells promote innate immunity in the gut. Immunity (2011) 34:122–34. doi:10.1016/j.immuni.2010.12.009
30. Zheng Y, Valdez PA, Danilenko DM, Hu Y, Sa SM, Gong Q, et al. Interleukin-22 mediates early host defense against attaching and effacing bacterial pathogens. Nat Med (2008) 14:282–9. doi:10.1038/nm1720
31. Croxatto D, Micheletti A, Montaldo E, Orecchia P, Loiacono F, Canegallo F, et al. Group 3 innate lymphoid cells regulate neutrophil migration and function in human decidua. Mucosal Immunol (2016). doi:10.1038/mi.2016.10
32. Monticelli LA, Sonnenberg GF, Abt MC, Alenghat T, Ziegler CG, Doering TA, et al. Innate lymphoid cells promote lung-tissue homeostasis after infection with influenza virus. Nat Immunol (2011) 12:1045–54. doi:10.1031/ni.2131
33. Finke D. Fate and function of lymphoid tissue inducer cells. Curr Opin Immunol (2005) 17:144–50. doi:10.1016/j.coi.2005.01.006
34. Scandella E, Bolinger B, Lattmann E, Miller S, Favre S, Littman DR, et al. Restoration of lymphoid organ integrity through the interaction of lymphoid tissue-inducer cells with stroma of the T cell zone. Nat Immunol (2008) 9:667–75. doi:10.1038/ni.1605
35. Hanash AM, Dudakov JA, Hua G, O’Connor MH, Young LF, Singer NV, et al. Interleukin-22 protects intestinal stem cells from immune-mediated tissue damage and regulates sensitivity to graft versus host disease. Immunity (2012) 37:339–50. doi:10.1016/j.immuni.2012.05.028
36. Lindemans CA, Calafiore M, Mertelsmann AM, O’Connor MH, Dudakov JA, Jenq RR, et al. Interleukin-22 promotes intestinal-stem-cell-mediated epithelial regeneration. Nature (2015) 528:560–4. doi:10.1038/nature16460
37. Munneke JM, Bjorklund AT, Mjosberg JM, Garming-Legert K, Bernink JH, Blom B, et al. Activated innate lymphoid cells are associated with a reduced susceptibility to graft-versus-host disease. Blood (2014) 124:812–21. doi:10.1182/blood-2013-11-536888
38. Mohty M, Malard F, Savani BN. High-dose total body irradiation and myeloablative conditioning before allogeneic hematopoietic cell transplantation: time to rethink? Biol Blood Marrow Transplant (2015) 21:620–4. doi:10.1016/j.bbmt.2014.09.010
40. Rangel-Moreno J, de la Luz Garcia-Hernandez M, Ramos-Payan R, Biear J, Hernady E, Sangster MY, et al. Long-lasting impact of neonatal exposure to total body gamma radiation on secondary lymphoid organ structure and function. Radiat Res (2015) 184:352–66. doi:10.1667/RR14047.1
41. Dudakov JA, Hanash AM, Jenq RR, Young LF, Ghosh A, Singer NV, et al. Interleukin-22 drives endogenous thymic regeneration in mice. Science (2012) 336:91–5. doi:10.1126/science.1218004
42. Konya V, Mjosberg J. Innate lymphoid cells in graft-versus-host disease. Am J Transplant (2015) 15:2795–801. doi:10.1111/ajt.13394
43. Moretta F, Petronelli F, Lucarelli B, Pitisci A, Bertaina A, Locatelli F, et al. The generation of human innate lymphoid cells is influenced by the source of hematopoietic stem cells and by the use of G-CSF. Eur J Immunol (2016) 46:1271–8. doi:10.1002/eji.201546079
44. Bendall LJ, Bradstock KF. G-CSF: from granulopoietic stimulant to bone marrow stem cell mobilizing agent. Cytokine Growth Factor Rev (2014) 25:355–67. doi:10.1016/j.cytogfr.2014.07.011
45. Trabanelli S, Curti A, Lecciso M, Salome B, Riether C, Ochsenbein A, et al. CD127+ innate lymphoid cells are dysregulated in treatment naive acute myeloid leukemia patients at diagnosis. Haematologica (2015) 100:e257–60. doi:10.3324/haematol.2014.119602
46. Vitale C, Ambrosini P, Montaldo E, Ballerini F, Moretta L, Mingari MC. IL-1beta-releasing human acute myeloid leukemia blasts modulate natural killer cell differentiation from CD34+ precursors. Haematologica (2015) 100:e42–5. doi:10.3324/haematol.2014.110494
47. Vitale C, Chiossone L, Morreale G, Lanino E, Cottalasso F, Moretti S, et al. Analysis of the activating receptors and cytolytic function of human natural killer cells undergoing in vivo differentiation after allogeneic bone marrow transplantation. Eur J Immunol (2004) 34:455–60. doi:10.1002/eji.200324668
48. Wang H, Grzywacz B, Sukovich D, McCullar V, Cao Q, Lee AB, et al. The unexpected effect of cyclosporin A on CD56+CD16- and CD56+CD16+ natural killer cell subpopulations. Blood (2007) 110:1530–9. doi:10.1182/blood-2006-10-048173
49. Rankin LC, Groom JR, Chopin M, Herold MJ, Walker JA, Mielke LA, et al. The transcription factor T-bet is essential for the development of NKp46+ innate lymphocytes via the Notch pathway. Nat Immunol (2013) 14:389–95. doi:10.1038/ni.2545
50. Satoh-Takayama N, Serafini N, Verrier T, Rekiki A, Renauld JC, Frankel G, et al. The chemokine receptor CXCR6 controls the functional topography of interleukin-22 producing intestinal innate lymphoid cells. Immunity (2014) 41:776–88. doi:10.1016/j.immuni.2014.10.007
51. Rankin LC, Girard-Madoux MJ, Seillet C, Mielke LA, Kerdiles Y, Fenis A, et al. Complementarity and redundancy of IL-22-producing innate lymphoid cells. Nat Immunol (2016) 17:179–86. doi:10.1038/ni.3332
52. Orange JS. Natural killer cell deficiency. J Allergy Clin Immunol (2013) 132:515–25. doi:10.1016/j.jaci.2013.07.020 quiz 526
53. Chijioke O, Muller A, Feederle R, Barros MH, Krieg C, Emmel V, et al. Human natural killer cells prevent infectious mononucleosis features by targeting lytic Epstein-Barr virus infection. Cell Rep (2013) 5:1489–98. doi:10.1016/j.celrep.2013.11.041
54. Della Chiesa M, Sivori S, Carlomagno S, Moretta L, Moretta A. Activating KIRs and NKG2C in viral infections: toward NK cell memory? Front Immunol (2015) 6:573. doi:10.3389/fimmu.2015.00573
55. Foley B, Felices M, Cichocki F, Cooley S, Verneris MR, Miller JS. The biology of NK cells and their receptors affects clinical outcomes after hematopoietic cell transplantation (HCT). Immunol Rev (2014) 258:45–63. doi:10.1111/imr.12157
56. Palmer JM, Rajasekaran K, Thakar MS, Malarkannan S. Clinical relevance of natural killer cells following hematopoietic stem cell transplantation. J Cancer (2013) 4:25–35. doi:10.7150/jca.5049
57. Beck JC, Wagner JE, DeFor TE, Brunstein CG, Schleiss MR, Young JA, et al. Impact of cytomegalovirus (CMV) reactivation after umbilical cord blood transplantation. Biol Blood Marrow Transplant (2010) 16:215–22. doi:10.1016/j.bbmt.2009.09.019
58. Beziat V, Dalgard O, Asselah T, Halfon P, Bedossa P, Boudifa A, et al. CMV drives clonal expansion of NKG2C+ NK cells expressing self-specific KIRs in chronic hepatitis patients. Eur J Immunol (2012) 42:447–57. doi:10.1002/eji.201141826
59. Beziat V, Liu LL, Malmberg JA, Ivarsson MA, Sohlberg E, Bjorklund AT, et al. NK cell responses to cytomegalovirus infection lead to stable imprints in the human KIR repertoire and involve activating KIRs. Blood (2013) 121:2678–88. doi:10.1182/blood-2012-10-459545
60. Bjorkstrom NK, Lindgren T, Stoltz M, Fauriat C, Braun M, Evander M, et al. Rapid expansion and long-term persistence of elevated NK cell numbers in humans infected with hantavirus. J Exp Med (2011) 208:13–21. doi:10.1084/jem.20100762
61. Bjorkstrom NK, Svensson A, Malmberg KJ, Eriksson K, Ljunggren HG. Characterization of natural killer cell phenotype and function during recurrent human HSV-2 infection. PLoS One (2011) 6:e27664. doi:10.1371/journal.pone.0027664
62. Della Chiesa M, Falco M, Bertaina A, Muccio L, Alicata C, Frassoni F, et al. Human cytomegalovirus infection promotes rapid maturation of NK cells expressing activating killer Ig-like receptor in patients transplanted with NKG2C-/- umbilical cord blood. J Immunol (2014) 192:1471–9. doi:10.4049/jimmunol.1302053
63. Della Chiesa M, Falco M, Podesta M, Locatelli F, Moretta L, Frassoni F, et al. Phenotypic and functional heterogeneity of human NK cells developing after umbilical cord blood transplantation: a role for human cytomegalovirus? Blood (2012) 119:399–410. doi:10.1182/blood-2011-08-372003
64. Foley B, Cooley S, Verneris MR, Curtsinger J, Luo X, Waller EK, et al. Human cytomegalovirus (CMV)-induced memory-like NKG2C(+) NK cells are transplantable and expand in vivo in response to recipient CMV antigen. J Immunol (2012) 189:5082–8. doi:10.4049/jimmunol.1201964
65. Foley B, Cooley S, Verneris MR, Pitt M, Curtsinger J, Luo X, et al. Cytomegalovirus reactivation after allogeneic transplantation promotes a lasting increase in educated NKG2C+ natural killer cells with potent function. Blood (2012) 119:2665–74. doi:10.1182/blood-2011-10-386995
66. Guma M, Angulo A, Vilches C, Gomez-Lozano N, Malats N, Lopez-Botet M. Imprint of human cytomegalovirus infection on the NK cell receptor repertoire. Blood (2004) 104:3664–71. doi:10.1182/blood-2004-05-2058
67. Muccio L, Bertaina A, Falco M, Pende D, Meazza R, Lopez-Botet M, et al. Analysis of memory-like natural killer cells in human cytomegalovirus-infected children undergoing αβ+T- and B-cell depleted HSCT for hematological malignancies. Haematologica (2016) 101:371–81. doi:10.3324/haematol.2015.134155
Keywords: hematopoietic stem cell transplantation, innate lymphoid cells, NK cells, GVHD
Citation: Vacca P, Montaldo E, Croxatto D, Moretta F, Bertaina A, Vitale C, Locatelli F, Mingari MC and Moretta L (2016) NK Cells and Other Innate Lymphoid Cells in Hematopoietic Stem Cell Transplantation. Front. Immunol. 7:188. doi: 10.3389/fimmu.2016.00188
Received: 19 February 2016; Accepted: 02 May 2016;
Published: 18 May 2016
Edited by:
Luigi Daniele Notarangelo, Harvard Medical School, USAReviewed by:
Andrew Gennery, Newcastle University, UKMette D. Hazenberg, Academic Medical Centre, Netherlands
Copyright: © 2016 Vacca, Montaldo, Croxatto, Moretta, Bertaina, Vitale, Locatelli, Mingari and Moretta. 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) or licensor 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: Paola Vacca, cGFvbGEudmFjY2EmI3gwMDA0MDt1bmlnZS5pdA==;
Lorenzo Moretta, bG9yZW56by5tb3JldHRhJiN4MDAwNDA7b3BiZy5uZXQ=
†Paola Vacca and Elisa Montaldo contributed equally.