- 1Department of Microbiology and Immunology, University of Montreal, Montreal, QC, Canada
- 2Research Center, Maisonneuve-Rosemont Hospital, Montreal, QC, Canada
- 3Department of Medicine, University of Montreal, Montreal, QC, Canada
- 4Division of Hematology and Oncology, Maisonneuve-Rosemont Hospital, Montreal, QC, Canada
A central objective in organ transplantation and the treatment or prevention of autoimmune disease is the achievement of antigen-specific immune tolerance. An additional challenge in bone marrow transplantation for the treatment of hematological malignancies is the prevention of graft-vs-host disease (GVHD) while maintaining graft-vs-tumor activity. Interestingly, CD4-CD8- (double negative, DN) T cells, which exhibit a unique antigen-specific immunoregulatory potential, appear to exhibit all of the properties to respond to these challenges. Herein, we review the therapeutic potential of immunoregulatory DN T cells in various immunopathological settings, including graft tolerance, GVHD, cancer, and autoimmunity.
Introduction
CD4-CD8- double negative (DN) T cells compose approximately 1–3% of total T cells in both mice and humans (Strober et al., 1989; Abraham et al., 1992; Fischer et al., 2005). Phenotypically, this rare T cell subset expresses a polyclonal αβT cell receptor (TCR) repertoire, lacks the expression of Foxp3 as well as natural killer (NK) cell markers and mostly presents with a naïve T cell phenotype (recently reviewed; Hillhouse and Lesage, 2012). Interestingly, their distinct phenotype, namely the lack of CD4 and CD8 co-receptors, is also believed to influence the method by which DN T cells recognize antigens and subsequently signal through their TCR. In fact, major histocompatibility complex (MHC) restriction is the cardinal feature of antigen recognition by T cells, where the CD4 and CD8 co-receptors respectively facilitate the interaction with MHC class II and I molecules. As DN T cells lack both CD4 and CD8 co-receptors, the means by which the αβTCR on the DN T cell recognizes MHC ligands with sufficient affinity and avidity to provide activation of DN T cells is unclear. It has been recently proposed that DN T cells recognize non-MHC ligands. Indeed, using quad-deficient mice that lack the expression of CD4 and CD8 co-receptors as well as MHC class I and II expression, Van Laethem et al. (2007) demonstrated that T cell development could proceed in an MHC-independent manner. In fact, in the absence of CD4 or CD8 co-receptor expression, the intracellular tyrosine kinase Lck is no longer sequestered by the co-receptors and is thus available to promote MHC-independent TCR signaling in thymocytes. Subsequently, these thymocytes develop into mature DN T cells that enter the periphery (Van Laethem et al., 2007). The ability of DN T cells to recognize non-MHC ligands is also supported by the finding that mature DN T cells from quad-deficient mice proliferate vigorously against both MHC-sufficient and MHC-deficient stimulator cells, but not in the absence of stimulator cells (Van Laethem et al., 2007; Tikhonova et al., 2012). In fact, a recent study has revealed the native self-protein CD155 as at least one of the ligands recognized by quad-deficient DN T cells via their TCR and in the absence of antigen-processing (Tikhonova et al., 2012). Therefore, the quad-deficient mouse model has helped to demonstrate that DN T cell differentiation can proceed in the thymus and that DN T cell activation can occur independently of co-receptors.
Double negative T cells have not only been observed in quad-deficient mice. For instance, an increased number of DN T cells has been observed in many TCR transgenic models (Hillhouse and Lesage, 2012). In these TCR transgenic models, due to forced expression of an αβTCR transgene, the DN T cells do recognize peptide–MHC complexes in the absence of co-receptor expression, suggesting that they exhibit a high affinity for these antigenic complexes. Moreover, in the absence of CD28 co-stimulation which is required for clonal deletion of thymocytes (Punt et al., 1994; Kishimoto and Sprent, 1997; Lesage et al., 1997), some thymocytes that strongly recognize self-ligands survive negative selection and ultimately develop into mature thymic DN T cells (Pobezinsky et al., 2012). Together, these results suggest that DN T cells may exhibit a relatively strong affinity toward their cognate ligands. This property is reminiscent of CD4+ Foxp3+ regulatory T cells (Tregs) and NKT cells, two immunoregulatory T cell subsets which undergo agonist selection in the thymus (Baldwin et al., 2004).
In addition to their distinct phenotype, DN T cells also exhibit a unique antigen-specific immunoregulatory potential. Indeed, the immunoregulatory function of DN T cells was first identified almost 25 years ago, when Strober et al. (1989) successfully cloned DN T cells from mice and subsequently demonstrated that DN T cells mediate suppressor activity in a mixed-lymphocyte reaction (MLR). Subsequently, Dr. Zhang’s group was the first to reveal the antigen-specific immunoregulatory potential of DN T cells (Zhang et al., 2000). Specifically, they showed that DN T cells from 2C TCR transgenic mice suppress the proliferation and cytotoxic activity of 2C TCR CD8+ T cells in vitro, but not of CD8+ T cells carrying other antigen specificities (Zhang et al., 2000; Young and Zhang, 2002). Moreover, the antigen-specific property of 2C TCR DN T cells is conferred, at least in part, by their ability to acquire peptide–MHC complexes from antigen presenting cells (Zhang et al., 2000; Priatel et al., 2001; Young and Zhang, 2002; Ford McIntyre et al., 2008), a process known as trogocytosis (Joly and Hudrisier, 2003). Notably, the in vitro antigen-specific suppressive activity of 2C TCR DN T cells toward CD8+ T cells was replicated using non-transgenic mice and humans (Zhang et al., 2000; Young and Zhang, 2002; Fischer et al., 2005). Together, these observations described a unique antigen-specific mode of immunoregulation provided by DN T cells, leading to the antigen-specific elimination of CD8+ T cells (Zhang et al., 2000; Young and Zhang, 2002).
The immunoregulatory potential of DN T cells has since been shown to extend beyond T cells. Indeed, TCR transgenic and non-transgenic DN T cells can also inhibit NK cells (He et al., 2007; Su et al., 2012), B cells (Zhang et al., 2006; Hillhouse et al., 2010; Ford McIntyre et al., 2011), and dendritic cells (Gao et al., 2011). The combination of their distinct phenotypic characteristics and their unique antigen-specific immunoregulatory properties toward multiple cellular targets has prompted investigators to examine the role of DN T cells in various disease models. Herein, we will review the promising therapeutic potential of DN T cells in the context of various disease settings. More specifically, we will describe the impact of DN T cell transfer on the induction of graft tolerance and the prevention of autoimmunity as well as present their dual role in preventing graft-vs-host disease (GVHD) while promoting graft-vs-tumor (GvT) responses.
Graft Tolerance
Although better known for their use in hematopoietic cell transplantation to establish donor chimerism or treat neoplastic relapse, donor leukocyte infusions (DLI) have also been shown to improve allograft survival after solid organ transplantation (Fehr and Sykes, 2004). Among possible mechanisms linking donor leukocyte transfer and allograft tolerance, DN T cells have been shown to increase allograft acceptance in various experimental settings. In an attempt to understand why DLI has a positive outcome on allograft survival, Dr. Zhang’s group took advantage of the antigen-specific 2C TCR transgenic model (Yang et al., 1998, 1999), where the 2C TCR is alloreactive to the Ld MHC class I molecule (Sha et al., 1988). Predictably, skin grafts bearing a single MHC-mismatch at Ld are thus rapidly rejected by the 2C TCR recipient mice due to the expression of Ld MHC class I molecule on the donor skin cells (Yang et al., 1998, 1999; Figure 1A). However, the injection of donor spleen cells to the 2C TCR recipient mice prior to the skin graft efficiently induced antigen-specific allograft tolerance (Yang et al., 1998, 1999; Figure 1B). The antigen-specific tolerance to skin allografts induced by the transfer of donor T cells was proposed to be mediated by 2C TCR transgenic DN T cells as only the 2C TCR transgenic DN T cell subset, but not the 2C CD4+ or 2C CD8+ T cell subset, was able to suppress an MLR response in vitro (Zhang et al., 2000). Accordingly, Zhang’s group showed that the injection of 2C TCR F1 DN T cell clones was sufficient to induce both prolonged survival of both skin and cardiac allografts (Zhang et al., 2000; Chen et al., 2003b; Figure 1C). Importantly, the allograft tolerance was antigen-specific, as full MHC-mismatched third party grafts were rapidly rejected (Zhang et al., 2000; Figure 1C). Collectively, these data demonstrate that 2C DN T cells are sufficient to induce both skin and cardiac allograft survival, suggesting that immunoregulatory DN T cells contribute to the benefits of DLI on allograft survival.
FIGURE 1. Induction of allograft tolerance by the pre-transplantation infusion of donor-specific spleen cells or DN T cells. This model takes advantage of the antigen-specific 2C TCR transgenic system and skin grafts to facilitate the study of allograft tolerance, where the 2C TCR transgene is alloreactive to the Ld MHC class I molecule. (A) C57BL/6 (H2b) mice are bred to BALB/c (H2d) mice to generate F1 mice (H2b,d) thus bearing the Ld MHC molecule (black mouse). C57BL/6 2C transgenic mice (H-2b) are bred to BALB/c (H2dm2) mice, which are a BALB/c Ld loss mutant (H2d, Ld-; Rubocki et al., 1986), to generate 2CF1 mice (H2b,d, Ld-) bearing the anti-Ld TCR (white mouse). Due to a single MHC-mismatch, skin grafts from Ld+ F1 mice are rapidly rejected by the 2CF1 mice. (B) However, the transfer of donor spleen cells from Ld+F1 mice to 2CF1 mice (Ld-) prior to the Ld+ skin graft transplantation results in graft survival. (C) Immunoregulatory 2C DN T cell clones obtained from 2CF1 TCR transgenic mice (Ld-) prevent the rejection of single MHC-mismatch, allogeneic (Ld+, in black) skin grafts. However, full MHC-mismatch, third party grafts (in gray) were rejected.
To further understand the mechanism by which 2C DN T cells promote antigen-specific allograft tolerance, Young et al. (2002) undertook the examination of the leukocytes found within the tolerated skin grafts. In doing so, they discovered that 2C DN T cells are the predominant leukocyte found within the accepted skin allografts. Moreover, the 2C DN T cells isolated from mice which had received donor spleen cells prior to the skin graft demonstrate an enhanced suppressive function toward 2C CD8+ T cells in vitro (Young et al., 2002). Finally, the comparison of transcriptome profiles between 2C TCR F1 DN T cells clones that are able or unable to confer cardiac allograft tolerance revealed FcRγ as a potential molecule involved in defining the tolerogenic potential of 2C DN T cells (Lee et al., 2005). The importance of FcRγ expression on 2C DN T cells for the induction of allograft tolerance was confirmed as the adoptive transfer of FcRγ-sufficient, but not FcRγ-deficient, 2C DN T cells prior to transplantation increased skin allograft survival (Thomson et al., 2006). Altogether, these results demonstrate that 2C DN T cells participate in allograft tolerance, likely by inhibiting pathogenic 2C CD8+ T cell responses, at least in the MHC class I-restricted graft tolerance model (Hillhouse and Lesage, 2012).
Importantly, these observations were not limited to the 2C TCR transgenic setting. Indeed, the injection of allogeneic donor spleen cells bearing a single MHC class I mismatch prior to skin transplantation in the non-transgenic setting also resulted in prolonged allograft survival (Yang et al., 1999; Young et al., 2002; Zhang et al., 2002). Analogous to the 2C TCR model, DN T cells from non-transgenic mice that are activated in vivo following the injection of donor spleen cells preferentially accumulate within the skin allograft and eliminate CD8+ T cells in an antigen-specific manner in vitro (Young et al., 2002). In a full MHC-mismatch heart allograft, injection of non-transgenic DN T cells further promoted rapamycin-induced graft tolerance (Zhang et al., 2011b). In addition, in vitro-generated DN T cells can also provide antigen-specific skin and pancreatic islet allograft tolerance (Zhang et al., 2007, 2011a). Moreover, with regards to xenografts, the injection of non-transgenic rat donor spleen cells in mice prevented CD4+ T cell-mediated cardiac xenograft rejection (Chen et al., 2003a, 2005). Similar to the transgenic setting, xenograft tolerance was induced by DN T cells, as the transfer of DN T cells that had been isolated from mice which had received xenogeneic donor spleen cells, was sufficient to ensure cardiac xenograft tolerance (Chen et al., 2003a). In this xenogeneic model, DN T cells efficiently suppressed the proliferation of both CD4+ and CD8+ T cell anti-donor reactive cells (Chen et al., 2003a, 2005). Using a variant of this cardiac xenograft model, it was also shown that DN T cells can eliminate B cells, leading to a reduction in anti-donor-specific antibody levels and delayed graft rejection (Ma et al., 2008). Taken together, these findings suggest that, as opposed to the MHC class I-restricted 2C TCR DN T cells, DN T cells from non-transgenic mice can suppress CD4+ and CD8+ T cells as well as B cells in an antigen-specific manner and potently suppress both skin and cardiac allograft, as well as cardiac xenograft, rejection.
Fas–FasL interactions have been proposed as the molecular mechanism by which DN T cells eliminate anti-donor T cells, while the elimination of B cells is considered to be perforin-mediated (Zhang et al., 2000, 2006; Priatel et al., 2001; Ma et al., 2008; Ford McIntyre et al., 2011). Interestingly, an accumulation of DN T cells is observed in both Fas- and FasL-deficient mice (Watanabe-Fukunaga et al., 1992; Takahashi et al., 1994), suggesting that the Fas–FasL pathway may regulate the number of DN T cells in vivo. By taking advantage of lpr mice, which exhibit a Fas-deficiency, Ford et al. (2002) demonstrated that DN T cells from lpr mice can mediate their immunoregulatory function through the Fas pathway as long as the target T cells express a functional Fas protein. Indeed, DN T cells from lpr mice could effectively delay both single MHC class I- and single MHC class II-mismatched skin allograft rejection (Ford et al., 2002). In summary, DN T cells can clearly induce an antigen-specific tolerance to both allografts and xenografts by eliminating or inhibiting the function of various target immune cells.
Autoimmunity
The antigen-specific immunoregulatory potential of DN T cells in graft tolerance suggests that they may also participate in the induction of immune tolerance in various autoimmune settings. As a result, the role of DN T cells has been mostly explored in autoimmune lymphoproliferative syndrome (ALPS), systemic lupus erythematosus (SLE) and mouse models of type 1 diabetes (T1D), as described below.
Autoimmune Lymphoproliferative Syndrome
Autoimmune lymphoproliferative syndrome is a rare disorder characterized by mutations in either Fas or FasL (Rieux-Laucat et al., 1995; Del-Rey et al., 2006), which results in defective Fas-mediated apoptosis and, consequently, the abnormal accumulation of activated lymphocytes. ALPS patients on average present with a 10-fold increase in DN T cell proportion (Bleesing et al., 2001a; Bristeau-Leprince et al., 2008; Magerus-Chatinet et al., 2009) and a sizeable proportion of DN T cells can also be found in the lymphoid organs of the murine models for ALPS, namely lpr/lpr (Fas-deficient) and gld/gld (FasL-deficient) mice (Cohen and Eisenberg, 1992; Watanabe-Fukunaga et al., 1992; Takahashi et al., 1994). Moreover, a greater proportion of DN T cells from ALPS patients, in comparison to healthy controls, express the B cell antigen, B220 (Bleesing et al., 2001a), which is consistent with findings in lpr/lpr mice (Davidson et al., 1986). Accordingly, B220 expression is a general feature of proliferating T cells (Bleesing et al., 2001b), which explains why B220+ DN T cells can also be found in healthy individuals. Although it cannot be denied that a drastic increase in the proportion of DN T cells can be observed in lpr/lpr and gld/gld mice, as well as ALPS patients, there is arguably no evidence to suggest that the accumulation of DN T cells is pathogenic. Indeed, Fas-deficient DN T cells found in lpr/lpr mice, but not FasL-deficient DN T cells found in gld/gld mice, remain functional and, as mentioned above, can efficiently induce graft tolerance (Ford et al., 2002). Hence, as DN T cell-mediated suppression depends on interactions between FasL on DN T cells and Fas on target T cells (Ford et al., 2002), it has been suggested that DN T cells accumulate in an attempt to compensate for their inability to suppress autoimmune T cells in lpr/lpr mice (Ford et al., 2002).
Systemic Lupus Erythematosus
Similar to ALPS patients, DN T cells are also found in greater numbers in the peripheral blood of patients with SLE (Crispin et al., 2008). However, in the case of SLE, these DN T cells are major producers of IL-17 (Crispin and Tsokos, 2009), which is pathogenic in this disease (Wong et al., 2000; Doreau et al., 2009). Moreover, IL-17-producing DN T cells can be found in the kidney sections of patients with lupus nephritis (Crispin et al., 2008). These results lead Crispin et al. (2008) to suggest that DN T cells themselves are pathogenic in SLE. Yet, it must be noted that, in these studies, DN T cells were defined as CD4-CD8-TCRαβ+ cells, which may contain contaminating CD4-CD8- NKT cells expressing a TCR restricted to CD1d molecules (Hillhouse and Lesage, 2012). Of relevance, NKT cells do indeed include a subset of CD4-NK1.1- IL-17-producing cells (Coquet et al., 2008). Moreover, NKT cells have been implicated in SLE pathogenesis where the activation of NKT cells through the administration of α-GalCer exacerbated disease whereas the inhibition of NKT cell activation using an anti-CD1d blocking antibody resulted in disease amelioration (Zeng et al., 2003). Thus, NKT cells cannot be ruled out as the true IL-17-producing cell subset in this particular study. Nevertheless, IL-17-producing DN T cells have also been shown to play a protective role against bacterial infections (Cowley et al., 2005; Riol-Blanco et al., 2010). Altogether, an uncertain, yet possible, role for DN T cells in patients with SLE remains to be defined.
Type 1 Diabetes
Type 1 diabetes occurs as a result of the antigen-specific elimination of pancreatic insulin-producing β cells. It thus presents as a relevant model to investigate the antigen-specific immunoregulatory potential of DN T cells.
The tolerogenic role of DN T cells in the prevention of T1D was first revealed using the P14/RIP-gp transgenic mouse model (Ohashi et al., 1991), where the MHC class I-restricted P14 TCR transgene recognizes the lymphocytic choriomeningitis virus (LCMV) protein, gp33–41 (gp33), which is expressed under the rat insulin promoter (RIP) forcing its expression in the pancreatic tissue. RIP-gp mice that are crossed to P14 mice carry a very high percentage of gp33-reactive T cells, yet the resulting P14 TCR:RIP-gp mice do not spontaneously develop diabetes on the C57BL/6 background (Ohashi et al., 1991). Indeed, P14/RIP-gp transgenic mice rapidly develop diabetes upon treatment with gp33 peptide and anti-CD40 agonistic antibody, which results in the infiltration of pancreatic islets by activated CD8+ T cells and the subsequent destruction of the insulin-producing β cells (Garza et al., 2000). Using this model, it was shown that the transfer of gp33 activated P14 DN T cells 1 day prior to diabetes induction can inhibit diabetes development (Ford et al., 2007). These results were the first indication that DN T cells may participate in the prevention of a CD8+ T cell-driven T1D pathology, further lending support for a potential role for DN T cells toward the elimination of CD8+ T cells in vivo.
The protective role of DN T cells in diabetes development was further investigated by our group using the 3A9 TCR:insHEL transgenic system, in which the MHC class II-restricted 3A9 TCR transgene recognizes a peptide from hen egg lysozyme (HEL) presented by I-Ak, while the insHEL transgene forces the expression of HEL in the pancreatic tissue. Although TCR:insHEL BALB.K mice are relatively resistant to T1D, CD47-deficient TCR:insHEL BALB.K mice have a high and spontaneous incidence of diabetes. Using this model of spontaneous T1D, a single transfer of 3A9 DN T cells in the TCR:insHEL CD47-deficient BALB.K transgenic model was able to significantly inhibit the development of T1D (Dugas et al., 2010). Notably, a 3A9 DN T cell transfer led to a significant reduction in antigen-specific autoantibody serum levels (Dugas et al., 2010), suggesting the in vivo elimination of autoreactive B cells. We subsequently demonstrated that 3A9 DN T cells efficiently eliminate HEL-loaded B cells in vitro (Hillhouse et al., 2010). Although this model is imperfect in that it is a CD47-deficient model, where CD47 is implicated in apoptosis, phagocytosis, cell migration, and T cell responses (Oldenborg, 2004; Chao et al., 2012), it is nevertheless a spontaneous model of T1D wherein the results complement the findings of Ford et al. (2007) suggesting that DN T cells may be of therapeutic interest for T1D.
Interestingly, the proportion of DN T cells is significantly reduced in diabetes-prone mice in comparison to diabetes-resistant mice in both the transgenic and non-transgenic systems (Dugas et al., 2010). It is of relevance that both the non-transgenic and TCR:insHEL transgenic diabetes-prone non-obese diabetic (NOD) mouse models exhibit a low number of DN T cells relative to other diabetes-resistant strains as it suggests that low DN T cell numbers are associated with diabetes susceptibility. Despite a reduction in cell number, 3A9 DN T cells from 3A9 TCR transgenic NOD. H2k mice carrying a diabetes-prone genetic background (Lesage et al., 2002) exhibit an equally potent cytotoxic function in comparison to 3A9 DN T cells from diabetes-resistant 3A9 TCR transgenic B10.Br mice (Hillhouse et al., 2010). Therefore, the association of DN T cells with diabetes susceptibility is due to a deficiency in DN T cell number rather than function. Altogether, these results further suggest that the restoration of DN T cell number can prevent T1D development in otherwise diabetes-susceptible mice.
The role of DN T cells in the prevention of T1D was also recently evaluated using non-transgenic DN T cells. Indeed, Duncan et al. (2010) have demonstrated that non-transgenic DN T cells can protect from autoimmune diabetes. Specifically, diabetes induction was inhibited if DN T cells were transferred into recipient NOD.SCID (severe combined immunodeficiency) mice 1 month prior to co-infusion with diabetogenic spleen cells, whereas the simultaneous co-infusion of diabetogenic spleen cells and DN T cells does not protect from disease (Duncan et al., 2010). However, as NKT cells were not fully excluded from the cellular preparation, additional studies using NKT cell-depleted non-transgenic DN T cells are warranted to firmly establish the biological function of these cells in the prevention of autoimmune diabetes in diabetes-susceptible NOD mice. Notably, further investigation is still needed to verify the role of DN T cells in T1D development using non-lymphopenic NOD mice, thus under more physiological and spontaneous conditions. Nevertheless, these results do provide useful information regarding the critical time of treatment initiation as well as evidence that non-transgenic DN T cells may exhibit the potential to inhibit T1D development in non-transgenic mice.
A more recent study further evaluated the role of non-transgenic DN T cells in T1D. Here, it was shown that 50% of CD4+ T cells isolated from an MLR had been converted to CD4-CD8- T cells. These CD4+ T cell-converted DN T cells sorted by flow cytometry were shown to delay T1D onset when adoptively transferred to NOD.SCID mice in combination with diabetogenic T cells (Zhang et al., 2011a). This delay was further enhanced when using GAD65 antigen to stimulate the CD4+ T cells, thereby likely generating a higher proportion of GAD65-specific DN T cells. Moreover, a single transfer of GAD65-specific DN T cells specificity was able to prevent diabetes development in 5-week-old NOD mice and decrease blood glucose levels in new-onset diabetic NOD mice (Zhang et al., 2011a). Therefore, this study offers a potentially translatable therapeutic approach for the generation of antigen-specific DNT cells in the prevention and treatment of T1D.
Altogether, these findings point toward an antigen-specific immunoregulatory role for DN T cells in autoimmune diseases. The therapeutic potential of these cells certainly merits further investigation in additional pre-clinical models.
Graft-vs-Host Disease and Cancer
In the treatment of hematological malignancies, allogeneic hematopoietic cell transplantation (AHCT) can eradicate several blood cancers that are incurable by chemotherapy alone. Despite indisputable successes, the efficacy of AHCT is still limited by cancer recurrence and the development of GVHD (Raiola et al., 2003). While the acute form of GVHD is triggered by direct T cell recognition of histocompatibility antigens, the pathophysiology of chronic GVHD remains more elusive and relies on several immune cell types (Shlomchik, 2007). Currently, 40–80% of patients develop chronic GVHD after AHCT, which brings substantial morbidity and mortality (Lee, 2005). Several lines of evidence suggest that immunoregulatory immune cells are paramount to GVHD prevention. Indeed, both CD4+ Tregs and NKT cells have been suggested as major contributors of allotolerance in hematopoietic cell transplantation (Hoffmann et al., 2002; Kohrt et al., 2010; Di Ianni et al., 2011; Chaidos et al., 2012). However, the ability of Tregs to maintain their anti-tumor T cell responses remains controversial (Onizuka et al., 1999; Shimizu et al., 1999; Liyanage et al., 2002; Somasundaram et al., 2002; Kohrt et al., 2010). Here, we review the potential of DN T cells at inhibiting GVHD while specifically promoting anti-tumor responses.
Graft-vs-Host Disease
Mouse models of GVHD, although they admittedly do not fully replicate human disease, facilitate the examination of the cellular process amid the allogeneic responses which give rise to a GVHD-like pathology in vivo (Shlomchik, 2007). A potential role for DN T cells in the prevention of GVHD can be traced back to over two decades ago when Bruley-Rosset et al. (1990) demonstrated that transfer of spleen cells from pre-immunized mice was able to inhibit GVHD only when DN T cells were included in the cellular preparations. Although the DN T cells were not void of contaminating NKT cells, these results still suggested that DN T cells play a role in GVHD prevention. Because of their prominent antigen-specific immunoregulatory potential as well as their ability to promote allotolerance, the contribution of DN T cells at preventing GVHD was later investigated using the 2C TCR single MHC-mismatch model (Young et al., 2003a), for which DN T cells have been shown to effectively prevent allograft rejection (Zhang et al., 2000; Young et al., 2002; Chen et al., 2003b; Figure 1). Specifically, mice bearing a single MHC-mismatch (Ld) injected with Ld-specific 2C TCR transgenic spleen cells survived for more than 150 days without any clinical or histological signs of acute or chronic GVHD (Young et al., 2003a; Figure 2A). The tolerance of donor spleen cells may be explained, at least in part, by the accumulation of 2C TCR DN T cells, which can effectively inhibit pathogenic CD8+ T cell responses, in recipient mice (Young et al., 2003a). Subsequently, the role of non-transgenic DN T cells in both parent to F1 and fully MHC-mismatched bone marrow (BM) transplantation following either a myeloablative (He et al., 2007) or non-myeloablative regimen (Su et al., 2012) was investigated (Figure 2B). In stark contrast to CD4+ and CD8+ T cells, the co-injection of non-transgenic DN T cells with T cell-depleted BM into a sublethally irradiated host ensured prolonged recipient survival in the absence of clinical signs of GVHD (He et al., 2007; Su et al., 2012; Figure 2B), indicating that DN T cells are not alloreactive nor pathogenic in this context. Moreover, this led to stable mixed chimerism and, as opposed to BM transplantation alone, promoted donor allotolerance (He et al., 2007; Su et al., 2012; Figure 2B). Together, these findings demonstrate that, as opposed to CD4+ or CD8+ T cells, the transfer of allogeneic DN T cells does not cause GVHD. Rather, DN T cells prevent GVHD, induce mixed chimerism and promote donor-specific allotolerance.
FIGURE 2. Double negative T cells promote tolerance while inhibiting GVHD. (A) Immunodeficient SCID F1 mice (H2b,d, Ld+) were sublethally irradiated and reconstituted with 2CF1 (H2b,dm2, Ld-) Ld-specific spleen cells. Three weeks later, recipient mice were given skin grafts from F1 (Ld+, in white) and full MHC-mismatch, third party (in gray) mice. The third party skin graft was rejected, whereas the skin graft from the F1 (Ld+) donor mouse was accepted. Importantly, the recipient mice showed no signs of GVHD and exhibited a prominent increase in the levels of donor-derived DN T cells over time. (B) BALB/c (H2d) mice underwent myeloablative (top panel, sublethal irradiation) or non-myeloablative (bottom panel, busulfan treatment) conditioning prior to being reconstituted with a combination of C57BL/6 (H2b) DN T cells and T cell-depleted (TCD) C57BL/6 (H2b) bone marrow (BM) cells. Subsequently, recipient mice received skin grafts from donor C57BL/6 (H2b, in black) and third party (H2k, in gray) mice. Regardless of the type of conditioning regimen utilized, the recipient mice accepted all C57BL/6 (H2b, in black) donor grafts while third party (H2k, in gray) grafts were rejected.
Notably, there is accrued evidence that DN T cells also prevent GVHD in humans upon AHCT. Indeed, the stem cells used for AHCT are currently most commonly obtained from the peripheral blood mononuclear cells of granulocyte colony-stimulating factor (G-CSF)-treated donors, where G-CSF is used to mobilize CD34+ hematopoietic stem cells into the blood (Shlomchik, 2007). Interestingly, in addition to skewing toward a Th2 phenotype, G-CSF treatment also results in an increase in the proportion of immunoregulatory DN T cells in the blood (Kusnierz-Glaz et al., 1997). The combination of these two phenotypes may explain why the transfer of CD34+ stem cells isolated following G-CSF treatment does not increase the incidence of acute GVHD relative to classical BM transplants. More recently, two studies also noted a clear correlation between an elevated proportion of DN T cells and a low incidence of GVHD development following AHCT (McIver et al., 2008; Ye et al., 2011). Together, these observations support the view that human DN T cells may prevent GVHD.
The Anti-Tumor Response
In addition to preventing GVHD, DN T cells demonstrate an anti-tumor activity without causing GVHD in recipient mice (Young et al., 2001, 2003b). Indeed, >90% of sublethally irradiated immunodeficient SCID mice that were co-infused with a lethal dose of A20 lymphoma cells together with allogeneic 2C TCR transgenic spleen cells survived indefinitely in the absence of GVHD. Interestingly, recipient mice exhibited a 15-fold increase in the number of DN T cells in their spleen (Young et al., 2003b), suggesting an association between DN T cells and the inhibition of GVHD as well as tumor growth. Accordingly, Young et al. (2003b) demonstrated that the injection of either 2C DN T cell clones or non-transgenic DN T cells was sufficient to prevent A20 lymphoma tumor growth, without inducing clinical or histological signs of GVHD. Altogether, these results further demonstrate the anti-tumoral potential of DN T cells.
To further define the potential use of DN T cells in the treatment of hematological malignancies, Merims et al. (2011) performed a pre-clinical study in acute myeloid leukemia (AML) patients undergoing complete remission following standard chemotherapy. In this study, they demonstrate that DN T cells can be readily isolated from the blood of AML patients. Moreover, the isolated DN T cells maintain their phenotype following a proficient cellular expansion reaching nearly 500-fold in 2 weeks (Merims et al., 2011). Of interest, the DN T cells isolated and expanded in vitro demonstrated efficient cytolytic activity toward the autologous leukemic cells in six out of seven patients (Merims et al., 2011). Importantly, the anti-tumoral activity of DN T cells may extend beyond hematological malignancies, as melanoma-reactive DN T cells have also been successfully isolated from a previously immunized melanoma patient (Voelkl et al., 2009). The mechanism by which DN T cells are able to confer antigen-specific immune tolerance all the while providing an anti-tumor response is counterintuitive and certainly merits further investigation.
Conclusion
Immunoregulatory DN T cells, which compose approximately 1–3% of T cells in human PBMCs (Fischer et al., 2005), demonstrate a unique antigen-specific therapeutic potential, such that they provide a favorable outcome in graft tolerance, autoimmunity and GVHD. In addition, DN T cells exhibit an interesting anti-tumoral potential. This seemingly broad applicability of DN T cells at conferring antigen-specific immune tolerance must be interpreted with caution. Indeed, DN T cells compose a heterogeneous subset of cells, which include all CD4-CD8-CD3+ T cell subsets, namely TCRγδ T cells, NKT cells and immunoregulatory TCRαβ DN T cells (Hillhouse and Lesage, 2012). Despite the heterogeneity in the description of DN T cells in various studies, which do not always exclude TCRγδ and/or NKT cells, most studies in TCR transgenic and non-transgenic mice as well as in humans point toward an immunoregulatory role for DN T cells. A few notable exceptions to this are the description of pathogenic IL-17-producing DN T cells in SLE (Crispin and Tsokos, 2009) and the characterization of IL-23 responsive DN T cells controlling bacterial infections (Cowley et al., 2005, 2010; Riol-Blanco et al., 2010). Clearly, additional studies aimed at identifying unique markers for these unique cell types will help clarify which specific cellular subset contributes to each specific biological setting.
In conclusion, immunoregulatory DN T cells exhibit great potential as a cellular therapy for various models of disease, with exciting advances in the pre-clinical setting. As the function of DN T cells is mainly antigen-specific, the use of DN T cells in immunotherapy should lead to fewer side-effects and a decreased risk of infections, which is a major concern in the application of broad immunosuppressive regimens. Moreover, DN T cells exhibit a potent immunosuppressive potential in multiple model systems, from transplantation to autoimmunity, suggesting a vast array of applicability of DN T cells in cellular therapy.
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.
Acknowledgments
Erin E. Hillhouse is recipient of a Diabète Québec scholarship and was recipient of a PhD scholarship from the Canadian Institutes of Health Research. Jean-Sébastien Delisle is an awardee from the Fonds de recherche du Québec - Santé (FRQS) Junior-1 clinician-scientist and is supported by the Leukemia/Lymphoma Society of Canada. Sylvie Lesage holds a Canadian Institutes of Health Research New Investigator scholarship. Sylvie Lesage and Jean-Sébastien Delisle are both independently funded by the Foundation of the Maisonneuve-Rosemont Hospital and National Sciences and Engineering Research Council of Canada.
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Keywords: graft-vs-host disease, autoimmunity, cancer, graft tolerance, immunoregulation, double negative T cells
Citation: Hillhouse EE, Delisle J-S and Lesage S (2013) Immunoregulatory CD4-CD8- T cells as a potential therapeutic tool for transplantation, autoimmunity, and cancer. Front. Immun. 4:6. doi: 10.3389/fimmu.2013.00006
Received: 09 November 2012; Paper pending published: 02 January 2013;
Accepted: 05 January 2013; Published online: 24 January 2013.
Edited by:
Lucienne Chatenoud, Université Paris Descartes, FranceCopyright: © 2013 Hillhouse, Delisle and Lesage. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
*Correspondence: Sylvie Lesage, Research Center, Maisonneuve-Rosemont Hospital, 5415 Boulevard de l’Assomption, Montreal, QC H1T 2M4, Canada. e-mail: sylvie.lesage@umontreal.ca, sylvie.lesage@gmail.com