Abstract
From mouse studies to recently published clinical trials, evidence has accumulated on the potential use of regulatory T cells (Treg) in preventing and treating graft-versus-host disease following hematopoietic-cell transplantation (HCT). However, controversies remain as to the phenotype and stability of various Treg subsets and their respective roles in vivo, the requirement of antigen-specificity of Treg to reduce promiscuous suppression, and the molecular mechanisms by which Treg suppress, particularly in humans. In this review, we discuss recent findings that support a heterogeneous population of human Treg, address advances in understanding how Treg function in the context of HCT, and present data on recent clinical trials that highlight the feasibility and limitations on Treg immunotherapy for graft-versus-host disease.
Introduction
Regulatory T cells (Treg) express the Forkhead box P3 (FOXP3) transcription factor and are indispensable for self-tolerance and the regulation of pathogenic immune responses [Sakaguchi et al. 2008]. They mainly do this by suppressing the proliferation and function of effector T cells [Vignali et al. 2008]. Given their ability to maintain and restore homeostasis in the immune system, Treg have the potential to ameliorate aberrant immune conditions such as autoimmunity and graft-versus-host disease (GvHD). It is feasible to isolate Treg based on key cell surface markers and to expand them to clinically relevant numbers. Administration of these cells in the murine model reduces GvHD, but their efficacy in humans is still uncertain. Correlative human studies to evaluate the association between in vivo Treg numbers and the incidence of GvHD have yielded varying results, although most studies suggest an inverse correlation between Treg numbers and GvHD (see Table 1). Recent clinical trials demonstrate the feasibility and general safety of adoptive transfer of Treg, but efficacy outcomes of GvHD and tumor immunity require further investigation. In this review, we provide insights into recent advances on the biology of Treg and discuss how these findings may impact the use of Treg in immunotherapy for GvHD.
Correlation between Treg numbers and incidence and severity of graft-versus-host disease.
GvHD, graft-versus-host disease; aGvHD, acute GvHD; cGvHD, chronic GvHD; PB, peripheral blood; PT, post-transplant; Treg, regulatory T cells.
Characterization of natural regulatory T cells
CD25
Sakaguchi and colleagues reported constitutive expression of a surface marker, CD25 (IL2Ralpha), on a subset of CD4 T cells that are suppressive [Sakaguchi et al. 1995]. These cells comprise approximately 1–10% of peripheral CD4 T cells in mice and humans. The level of CD25 expression correlates with suppressor function, with the top 5–10% representing the majority of the regulatory T cells. Hence, most early studies identified Treg as CD4CD25hi T cells, although the level of CD25 expression used to characterize or purify Treg is variable between studies, making comparisons of data and results less reliable. Nevertheless, CD4CD25hi T cells prevented and reduced autoimmunity, organ transplant rejection, and GvHD [Sakaguchi et al. 2008]. However, because T cells express CD25 upon activation, distinguishing regulatory T cells from activated effector T cells can be difficult based on this single marker.
FOXP3
The transcription factor, FOXP3, was found to be critical for Treg development and function in mouse models [Fontenot et al. 2003; Hori et al. 2003; Khattri et al. 2003], and hence provided a unique marker for Treg, although the intracellular localization of FOXP3 precludes its use in purifying Treg for functional studies. Activation of CD4+CD25- T cells does not lead to FOXP3 expression in the mouse, unlike CD25 [Khattri et al. 2003]. In humans, mutation of the FOXP3 gene causes a lymphoproliferative syndrome called IPEX (immune dysregulation, polyendocrinopathy, enterophy, and x-linked) [Sakaguchi et al. 2008]. However, FOXP3 expression in and of itself is inadequate to define human Treg, as naïve T cells without regulatory function can transiently upregulate FOXP3 upon activation [Gavin et al. 2006]. These findings have led to confusion on how to interpret results based on CD25 and FOXP3 expression in human Treg.
CD127 and CD45RA
CD127 (IL7 receptor alpha chain) and CD45RA have recently emerged as additional markers of Treg. In combination with high levels of CD25, low expression of CD127 is correlated with Treg that express FOXP3 [Liu et al. 2006; Seddiki et al. 2006]. However, conventional T cells can also reduce CD127 expression following activation ex vivo, limiting the ability to distinguish Treg from activated nonregulatory T cells [Mazzucchelli and Durum, 2007]. It is not clear whether this downregulation of CD127 occurs in vivo, particularly under inflammatory conditions such as GvHD. CD45RA and CD45RO are markers of maturity in human T cells and when used with CD25, define several subsets of Treg that share developmental origins but have distinct gene expression [Miyara et al. 2009]. CD4CD25intCD45RA+ and CD4CD25hiCD45RO have low and high FOXP3 expression and are defined as resting and activated Treg, respectively. Both Treg subsets are suppressive in vitro, but the resting Treg are resistant to apoptosis and can proliferate in culture, while activated Treg have a more differentiated effector phenotype and are hyporesponsive to TCR stimulation. Additional markers, such as CD31, ICOS, and HLA-DR define additional cell populations within the resting and activated Treg subsets that appear to have differential suppressor function [Miyara et al. 2009; Ito et al. 2008; Baecher-Allan et al. 2006]. Thus, it is becoming clear that there is a heterogeneous population of human Treg, but whose function and localization in vivo remain unclear.
Natural Treg versus inducible Treg
Natural Treg (nTreg) are generated in the thymus, while ‘inducible’ or ‘adaptive’ Treg (iTreg) are produced in secondary lymphoid organs and peripheral tissues upon exposure to transforming growth factor beta (TGFβ) and retinoic acid [Coombes et al. 2007]. Other agents have been studied to convert naïve CD4 T cells into iTreg. These include hypomethylating agents (i.e. decitabine), antithymocyte globulin, and vasoactive intestinal peptides, with further details provided in Table 2. Both Treg subsets are mediators of peripheral tolerance and homeostasis in mouse models, however, the relative extent to which nTreg and iTreg contribute in vivo is not clear. This has been in part due to the absence of definitive markers that distinguish these two Treg subsets. Based on microarray studies in the mouse, two markers have been identified to be more specific for nTreg compared with iTreg. These include Helios [Thornton et al. 2010], an intracellular molecule, and Neuropilin 1 (Nrp1) [Bruder et al. 2004], a surface protein. While increased expression of Helios is observed for both mouse and human nTreg, early studies indicate that Nrp1 is only specific for mouse but not human nTreg. These surface markers provide tools to characterize the likely phenotypic differences and functional specialization between nTreg and iTreg in vivo.
Strategies to induce or expand regulatory T cells and results in GvHD studies.
ECP, extracorporeal photophoresis; DC, dendritic cell; APC, antigen-presenting cell; PB, peripheral blood; GvHD, graft-versus-host disease; aGvHD, acute GvHD; cGvHD, chronic GvHD; Treg, regulatory T cells; iDC, immature dendritic cell; IL, interleukin; UCB, umbilical cord blood; TGF, transforming growth factor; IFN, interferon; BM, bone marrow.
In humans, the role of iTreg in vivo is not known. In vitro, human naïve CD4 T cells can be induced to express FOXP3 in the presence of TGFβ; however, these iTreg have reduced suppressor function in vitro and can secrete pro-inflammatory cytokines [Tran et al. 2007; Walker et al. 2005]. The addition of retinoic acid to the TGFβ condition appears to enhance stability and function of iTreg in vitro [Wang et al. 2009] however, whether this holds true in the in vivo setting, particularly under lymphopenic or inflammatory conditions, is not known. Also, these findings suggest that there may be other factors that are required to maintain stability of human iTreg.
Regulatory T-cell functional specialization
The mechanisms by which Treg suppress are complex, and include signaling via interleukin 10 (IL10), IL35, TGFβ, CD39, CTLA4, LAG3, Granzyme A and B, and perforin, among others. The details of these mechanisms are beyond the scope of this review, and were summarized recently [Vignali et al. 2008]. Most of the mechanistic studies were derived from mouse models. Our current understanding of how human Treg function remains limited to in vitro studies, which do not account for the importance of migration and localization in the development, differentiation, and function of Treg in vivo [Zhang et al. 2009]. Thus, questions remain on where adoptively transferred human Treg get primed, how they get there, and where they function. Some insights have been provided by mouse models of allogeneic tissue grafts [Zhang et al. 2009]. In these studies, nTreg enter the inflamed tissue before reaching the draining lymph node (LN). In contrast, iTreg first enter the LN before migrating to the site of inflammation. These observations suggest that nTreg and iTreg have different homing receptors at transfer that affect their site of priming and activation in vivo.
Recent studies indicate that there is a heterogeneous population of Treg with functional specialization [Campbell and Koch, 2011]. In particular, there are subsets of human Treg with distinct expression of transcription factors, cytokines, and chemokine receptors that parallel those expressed in subsets of helper T cells (Th). How and from whence these Treg develop and acquire similar phenotypic features of their Th counterpart requires further investigation. Preliminary studies suggest that nTreg responds to cytokines that are specific to the Th subset, for example, interferon gamma (IFNγ), and upregulate Tbet, a transcription factor normally expressed in Th1 cells, which promotes acquisition of homing receptors that allow accumulation of Treg at sites of Th1 mediated immunity [Koch et al. 2009]. These findings are relevant as we continue to define subsets of Treg that are most effective for different diseases.
As noted previously, nTreg and iTreg are developmentally different. Therefore, is not clear whether iTreg and nTreg share mechanisms of suppression. Because iTreg are generated by multiple pathways, some not dependent on FOXP3 expression, there are likely mechanisms of suppression that are unique to iTreg. One example is IL35, a cytokine consisting of IL27β and IL12α subunits, that are increased on Treg, but not conventional T cells. In both mouse and humans, IL35 induces iTreg, which continue to generate IL35 to sustain the iTreg population and function [Collison et al. 2010]. IL35-Treg do not express FOXP3 or IL10, but function in vivo with the same or higher suppressive capacity than nTreg. Other iTreg subsets that express FOXP3 are not as potent suppressor in vivo compared with nTreg and this is likely related to the functional dependence of these iTreg on FOXP3 expression, which is transient and unstable in vivo as described below. Under homeostatic conditions, IL35-Treg are not detected; they require very strong inflammatory conditions for induction and expansion [Collison et al. 2010]. Potential differences in nTreg and iTreg suppression suggest that they play nonoverlapping roles in vivo and therefore may have differential impact in different model systems.
The stability of the Treg phenotype and function in vivo remains in question [Sakaguchi, 2010]. Understanding this aspect of Treg biology is critical as we consider the subset(s) of Treg that can be used in adoptive transfer studies and in the clinical settings. In murine studies, nTreg appears to have a stable suppressor phenotype and function, even under inflammatory conditions [Rubtsov et al. 2010]. In contrast, both mouse and human studies indicate that FOXP3 expression in iTreg is more transient, and hence the suppressor function is inferior in vivo. This is particularly true under inflammatory or lymphopenic conditions, which are generally the setting under which iTreg would be adoptively transferred [Koenecke et al. 2009; Zhou et al. 2009; Tran et al. 2007; Walker et al. 2005]. Using FOXP3 lineage-tracer mice, it was shown that iTreg are less stable and become ‘ex-Treg’ that generate IFNγ and can induce diabetes in NOD mice [Zhou et al. 2009]. The plasticity of the iTreg must therefore be taken into account as we consider their use in vivo and in the clinical setting. iTreg subsets that are FOXP3 independent, however, can remain suppressive under inflammatory conditions such as the IL35 iTreg aforementioned.
GvHD, graft-versus-tumor, and Treg
Mouse studies
Early studies in various murine models of bone marrow transplantation indicate that adoptively transferred Treg can prevent and treat GvHD [Nguyen et al. 2007; Edinger et al. 2003; Jones et al. 2003; Cohen et al. 2002; Taylor et al. 2002]. The mechanisms by which Treg suppress GvHD is not entirely clear, but localization of Treg into secondary lymphoid organs [Taylor et al. 2004; Edinger et al. 2003] and peripheral tissues [Wysocki et al. 2005] are critical for their function. Bioluminescence imaging studies have provided insights into the kinetics of Treg in GvHD [Nguyen et al. 2007]. These studies demonstrate that Treg, purified as CD4+CD25hi cells, co-localize with conventional effector T cells (Tcon) in secondary lymphoid organs initially, where they expand robustly and then migrate into peripheral tissues such as the gut and skin. Their colocalization also led to the suppression of Tcon proliferation in both lymphoid and peripheral tissues. After approximately 7–10 days following transfer, there is a significant reduction in Treg numbers, which may due to a decreased inflammatory milieu. By bioluminescence imaging, these labeled Treg, although reduced, are still detectable 3 months following transfer and are found diffusely in peripheral tissues. These findings provided a framework for the design and development of some recent clinical trials for adoptive Treg transfer.
Correlative human studies
Many correlative studies have been published to establish an association between the level of Treg in various tissues and the incidence and/or severity of GvHD in patients. As detailed in Table 1, the results are conflicting and may be due to several reasons, particularly variability in the Treg phenotype, the time point at which they are analyzed, and the tissue from which they are extracted for analysis. Predominantly, most studies report on peripheral blood (PB) Treg number and percentages; however, the relevance of PB Treg and how they reflect Treg number and function in the tissue are not known, particularly in light of functional specialization and localization of different Treg subsets. Another caveat is that the kinetics of Treg and their role in causing or preventing disease in vivo cannot be captured by a single or even a few time points following transplantation. Therefore, it would difficult to determine whether low numbers of Treg in the gut of patients with GvHD can explain cause or effect based on these studies. Furthermore, strategies to purify or characterize ‘Treg’ are different between experiments or studies, complicating interpretation of the findings across studies. Nevertheless, the majority of the studies indicate an inverse correlation between Treg number or Treg:Tcon ratio and the incidence and severity of GvHD.
Phenotype and source of Treg for adoptive therapy
Most preclinical studies in transplantation transfer freshly isolated Treg. However, because Treg comprise a small fraction of CD4 T cells, a concern is an insufficient number of Treg that can be isolated for adoptive transfer in the clinical setting. To address this potential issue, based on preclinical data [Cohen et al. 2002; Taylor et al. 2002] current ongoing efforts are to expand nTreg under activating conditions with CD3/CD28 stimulation and IL2, or to induce naïve CD4+CD25- T cells under skewing conditions with high-dose TGFβ and/or retinoic acid that promote conversion into iTreg. Other strategies for expansion and conversion have recently been published and are detailed in Table 2. While expansion and conversion strategies generate significant numbers of Treg, there are issues of purity and in vivo functional stability for ex vivo expanded nTreg and iTreg, respectively.
As noted previously, multiple studies have demonstrated plasticity and lack of stability of the phenotype and function of iTreg in autoimmune models. Furthermore, in a recent study, iTreg generated ex vivo under TGFβ conditions reverted to a nonregulatory T-cell phenotype in vivo and failed to prevent GvHD in a murine model [Koenecke et al. 2009]. Thus, TGFβ-induced Treg do not appear to be a reliable source of suppressor cells for transfer under inflammatory and lymphopenic settings. However, as detailed in Table 2, there are a multitude of strategies that may induce a more stable phenotype but these strategies require further studies to confirm. For the induction of human Treg, several groups have demonstrated that a course of extracorporeal photopheresis could convert naïve T cells into iTreg in vivo [Rao et al. 2009; Biagi et al. 2007]. Other investigators showed stable iTreg induction with hypomethylating agents [Sanchez-Abarca et al. 2010], a promising strategy for translation in the clinical setting but requires further testing.
For ex vivo expanded nTreg, contamination with effector T cells in the culture system remains the major concern. In part, this is due to the imprecise selection of Treg based on CD25, since activated T cells also upregulate this marker. However, with additional markers such as CD127 and CD45RA as detailed previously, it may now be possible to increase the purity of sorted and expanded Treg for adoptive transfer studies [Hippen et al. 2011].
A second concern regarding expanded nTreg is the impact culturing may have on their homing and chemokine receptor expression, which could interfere with their effective entry into target tissues. In murine models of GvHD, expanded nTreg can suppress GvHD efficiently, albeit it appears that the major suppressive activity is due to the CD62Lhi Treg subset [Taylor et al. 2004]. Although one may postulate homing receptor expression would change with activation in vitro, a recent study and our own experience showed that activation of nTreg in vitro under CD3/CD28 costimulation does not significantly impact the chemokine receptor or selectin expression: CD62L expression remained high and there was no affect on the expression levels of CCR5, CCR6, CCR8, CLA, or CD103 [Cao et al. 2009]. Further studies are needed to confirm the in vivo homing capacity of expanded nTreg compared with freshly isolated Treg. Results may help determine the appropriate cell phenotype and dose for testing in the clinical trial setting since the ability of Treg to suppress in vivo depends on their ability to migrate to the right target tissue.
Until concerns of purity and stability of iTreg and expanded nTreg are addressed, freshly isolated nTreg are the most appropriate source for clinical trial. The optimal dose of Treg in the clinical setting is not known, but likely depends on the timing of adoptive transfer, the number effector T cells in the graft, and the tumor burden of the patient. While preclinical studies indicate that a 1:1 nTreg:Tcon ratio is effective in suppressing GvHD without abrogating the graft-versus-tumor response [Edinger et al. 2003; Cohen et al. 2002], it is not clear that this strategy would lead to similar outcomes in patients. Ongoing clinical trials of Treg immunotherapy will help establish this dose parameter.
Most preclinical studies and all clinical trials to date transfer polyclonal Treg into transplant recipients. Antigen-specific Treg (Ag-Treg) have been evaluated in autoimmune disease models to reduce nonspecific suppression of host immunity [Filippi et al. 2005]. For GvHD however, it is not currently possible to generate Ag-Treg given the lack of known immunodominant antigens and the multi-tissue expression of alloantigens and minor histocompatibility antigens that contribute \to the pathologic immune response. In models of GvHD, polyclonal Treg do not appear to compromise the GvT effect [Edinger et al. 2003; Cohen et al. 2002]. However, these studies were performed under contrived experimental conditions, with specific cell dose ratios and transplantable leukemia which may not be translatable to the clinical setting. Whether polyclonal Treg suppress tumor and microbial immunity following hematopoietic-cell transplantation (HCT) in the clinical setting remains unknown, and thus careful monitoring for relapse and infections are critical in trials incorporating Treg immunotherapy.
Clinical trials
Recently, two clinical trials reported on the outcomes of infusing Treg in patients undergoing haploidentical [Di Ianni et al. 2011] and double-cord HCT [Brunstein et al. 2011]. In the former study performed in Italy, 28 patients with hematological malignancies, primarily acute myeloid leukemia (AML), underwent myeloablative conditioning with total body irradiation (TBI), thiotepa, fludarabine, and cyclophosphamide followed by an infusion of freshly isolated CD4+CD25+ Treg from a haploidentical donor. After 4 days, the patient received infusions of CD34-selected progenitor cells and conventional CD3 T cells (Tcon) separately. This was a dose escalation phase I trial, with dose ratios of Treg:Tcon ranging from 4:1 to 2:1, with a maximum of 4 × 106/kg Treg given. The patients did not receive any post-transplant GvHD prophylaxis. With a median follow up of approximately 12 months, the authors report a reduction in GvHD compared with historical controls; no patients developed GvHD when 1 × 106/kg or less Tcon were given. Furthermore, donor immune reconstitution was timely, with earlier recovery of T cells specific to various opportunistic pathogens, including Aspergillus, cytomegalovirus (CMV), and adenovirus, congruent with preclinical data [Nguyen et al. 2008]. There were fewer CMV reactivations and no CMV-related mortality compared with their prior experience [Perruccio et al. 2005]. Overall, at a median follow up of 12 months, survival was 46%, with the majority of deaths due to infection, and the treatment related mortality (TRM) was 50%, which is higher than the reported 36.5% in their prior haploidentical HCT study [Aversa et al. 2005]. Leukemia relapse was not increased; however, longer follow up is required to determine the impact of Treg on the Graft versus leukemia (GvL) effect.
In the second clinical trial, Brunstein and colleagues reported results on the infusion of ex vivo expanded/activated umbilical-cord blood (UCB)-derived Treg [Brunstein et al. 2011]. A total of 23 patients with various leukemias underwent nonmyeloablative conditioning with low-dose TBI, cyclophosphamide, and fludarabine, followed by infusion of two HLA 4-6/6 UCB graft. From a third-party UCB, Treg were positively selected for CD25, expanded in culture with anti-CD3/anti-CD28 monoclonal antibody and recombinant IL2 over a 14-day period, and infused into the patient on day +1 of HCT. For 14 patients, a second infusion of Treg was given at day +15. This was a dose-escalation trial, with dose levels of 1, 3, 10, or 30 × 105 Treg/kg. GvHD prophylaxis consisted of mycophenolate mofetil (MMF) and cyclosporine in the first cohort, and MMF and sirolimus in a subsequent cohort based on reports that CsA may interfere with Treg function and survival [Coenen et al. 2006; Zeiser et al. 2006]. At a median follow up of approximately 1 year, Treg recipients had similar disease-free survival, long-term donor engraftment, and nonrelapse mortality compared with historical controls [Brunstein et al. 2007]. As with the trial by Di Ianni and colleagues, longer follow up is required to determine the impact of Treg on the GvL effect. While the incidence of grades II–IV acute GvHD was lowered in Treg-treated patients than historical controls, no difference was noted for grades III–IV acute GvHD. The role of Treg in chronic GvHD in this trial is not clear at the time of report given the short follow up.
Results from these two clinical trials indicate the feasibility of Treg infusions. However, the results also raise several questions of safety and efficacy. First, what are the reasons why relapse is not increased in Treg recipients? Overall, follow up in both studies is too short to conclude firmly. However, the infusion of Treg allowed the add-back of Tcon which may exert a GvL effect in the haploidentical HCT trial. In the UCB HCT, the authors show short-term survival of Treg of approximately 2 weeks following infusion; thus, perhaps the threshold of effector cells that survive are sufficient to mediate GvL. However, studies of the in vivo kinetics of Treg were limited to circulating Treg in the blood, and not in lymphoid or peripheral tissues where Treg reside and function. Thus, further investigation is needed to determine why Treg, particularly at the higher doses, do not impact tumor immunity in these two trials.
Second, in the haploidentical HCT trial, TRM was higher compared to historical controls, and are primarily due to opportunistic infections, even in the absence of standard immunosuppressive agents. Recent studies in viral infection models indicate that Treg can impair CD8 T-cell cytolytic activity, thus promoting chronic infection [Dietze et al. 2011]. It’s not clear whether Treg has similar effects on the mature donor Tcon which are important for early microbial immunity after transplant. However, differences in the preparative regimen and the patient population may also account for the increased TRM in this trial.
Third, in the UCB HCT clinical trial, the expanded Treg did not prevent high-grade acute GvHD compared with historical controls. This may be due to a variety of reasons, including timing of Treg infusion, differences in potency of fresh versus expanded Treg, the number and ratio of Treg relative to Tcon, and the purity of the Treg infused. In the haploidentical HCT trial, Treg were infused 4 days prior to Tcon, which likely increased the Treg:Tcon ratio based on Treg expansion during this lapsed time as shown in preclinical models [Nguyen et al. 2007]. In contrast, in the UCB HCT trial, Treg was infused 1 day after Tcon. In this situation, the earlier Tcon infusion may lead to early Tcon expansion, hence reducing the Treg:Tcon ratio. The timing of Treg therefore may have an impact on the final ratio of Treg:Tcon in vivo and affect GvHD outcomes. Furthermore, in the UBC HCT trial, the median proportion of CD4+CD25+ cells was 65% following CD25 selection, and the median proportion of CD4+CD127-FOXP3+ was 64% after culture. The ‘Treg’ product therefore likely consists of a significant proportion of Tcon which may offset the suppressive effects of Treg and may lead to outcomes that are more difficult to interpret. Improving the purity of the Treg population for adoptive transfer, either through flow-cytometric sorting or cultures under rapamycin conditions [Zeiser et al. 2008; Coenen et al. 2007; Battaglia et al. 2005] may address these concerns. Furthermore, performing a larger and randomized trial with long-term follow up will better at demonstrating the efficacy of Treg infusion.
Double UCB HCT typically leads to engraftment of a single unit at day 100 [Barker et al. 2005], suggesting rejection of the second unit by residual host cells, donor cells from the engrafted cord, or both. The biology of this engraftment dominance of a single unit is not well understood. In the UBC HCT trial by Brunstein and colleagues, the transferred Treg are derived from a third UCB unit. Analysis of the kinetics for the administered Treg indicates a reduction in both their absolute number and their percentage of total CD4 cells by day 14 post-HCT. While this decrease in Treg may be consistent with a reduction in inflammation further out from HCT, it does raise the question of whether third-party Treg are at risk for rejection by host residual cells or cells from the other two UCB units. Some preclinical findings suggest that third-party Treg may not be protective of engraftment [Gaidot et al. 2011; Joffre et al. 2004]; however, other studies in both mouse and xenogeneic models of GvHD show promise of third-party Treg as an effective ‘off-the-shelf’ therapy [Hippen et al. 2011; Steiner et al. 2006].
Ongoing trials are accessing the role of Treg in GvHD and other diseases, including diabetes and kidney transplant rejection. For diabetic patients, trials include adoptive transfer of polyclonal expanded autologous Treg (CD4+CD25+CD127lo) as a single infusion, or administration of low-dose IL2 to induce Treg in vivo. In the allogeneic HCT setting, studies include a phase 2 trial to test in vivo induction of Treg with low-dose IL2 as GvHD prophylaxis, and a phase 1 trial that transfers sorted freshly isolated polyclonal nTreg (CD4+CD25+CD127lo) into haploidentical graft recipients to allow higher doses of Tcon to be given without inducing GvHD.
Treg in evolving or established GvHD
Studies to date have primarily evaluated the role of Treg, given prophylactically, in reducing the incidence and severity of GvHD. The impact of Treg on established or evolving GvHD has been less studied [Nguyen et al. 2007; Jones et al. 2003]. When transferred into mice with established GvHD, Treg were less effective and while recipients of Treg had improved survival, end organ damage caused by GvHD was not reversed. In a case report, ex vivo expanded CD4+CD25+CD127- Treg were infused into two patients with steroid-refractory GvHD [Trzonkowski et al. 2009]. The first patient had grade IV acute GvHD and did not respond to three weekly infusions of 3 × 106 Treg/kg. The second patient with pulmonary chronic GvHD received a single dose of 1 × 105 Treg/kg, which lead to a reduction in symptoms and allowed tapering of multiple immunosuppressive agents. However, the long-term outcome of this patient is not known. These findings indicate that Treg immunotherapy may be optimal under prophylactic conditions.
Summary
Preclinical data indicate that Treg are a potent suppressor of GvHD that do not abrogate tumor and microbial immunity under specific dose ratios with Tcon. However, it remains unclear whether these outcomes would hold in the clinical setting, given our limited understanding of how human Treg function in vivo and challenges in achieving the desired cell dose ratios and purity. Moreover, unlike the mouse model, significant variability exists in our patients, including their genetics, disease, and the transplant and immunosuppressive regimens with which they are treated, all of which may have an impact on their response to Treg immunotherapy and other transplant outcomes. Two clinical trials offer preliminary observations which demonstrate the feasibility and safety of Treg infusion. However, long-term outcomes on efficacy and bystander effects on tumor and microbial immunity must be further addressed in randomized and larger trials. With emerging data on heterogeneous populations of human Treg with functional specialization, and as our ability to purify Treg advances with new markers, the benefit of Treg immunotherapy may rely on transferring specific subsets of Treg for different diseases, and even for different organs affected as is the case for GvHD. However, as with many cellular therapies, the labor- and cost-intensive process of generating the product may preclude their wide application to less-specialized centers and, as such, efforts to streamline this step must parallel our studies in understanding the biology and clinical use of Treg.
Footnotes
Acknowledgements
We thank Elizabeth Zale and Susan Cadle for their assistance in the preparation of the manuscript.
No funding/grant was provided for this work.
The authors declare no conflicts of interest in preparing this article.