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Université René Descartes Paris 5, INSERM U580, H?pital Necker-Enfants Malades, Paris, France.
Abstract
It is now well established that a distinct subset of T lymphocytes is essential for downregulating immune responses to both endogenous (self) and exogenous antigens. These Tregs are CD4+ and express high levels of CD25 (the chain of the IL-2 receptor) and the transcription factor Foxp3. The mechanisms determining the lifespan, homeostasis, and in vivo generation of these Tregs are still ill defined. A study by Vukmanovic-Stejic et al. in this issue of the JCI shows that in humans, Tregs are present throughout life but that despite their high throughput, they are short lived (see the related article beginning on page 2423). It is thus unlikely that all CD4+CD25hiFoxp3+ Tregs are generated as a separate lineage in the thymus. The authors propose that during adulthood, Tregs essentially emerge at the periphery from the memory T cell pool.
The existence in humans of naturally occurring CD4+CD25+ Tregs is highlighted by the rapid onset of a severe polyautoimmune syndrome in children genetically deficient for the transcription factor Foxp3, a lineage marker for this Treg subset. Based on this observation in humans and also on compelling experimental evidence obtained from the study of mice (1–4), it is postulated and generally accepted that Tregs are responsible for the control of autoreactive T cells, which react aggressively toward the host’s tissues and trigger autoimmune disease in the absence of effective T cell–mediated regulation.
A growing number of studies indicate that Tregs also play a significant role in downregulating the immune response to a variety of nonself antigens, such as microbial antigens, tumor antigens, and alloantigens (5–7). Some confusion persists, however, concerning the precise definition of the cell phenotype, functional capacity, and fine antigen specificity of the Tregs participating in these diverse contexts. The situation is further complicated by the fact that some studies argue for the participation of selective and distinct types of Tregs under each of these different conditions (8–13). In contrast, other studies adopt a more unifying view and propose that a single population of T cells, namely, thymus-derived CD4+CD25hiFoxp3+ T cells, gives rise to Tregs controlling the various immune responses (5).
It is apparent that these latter CD4+CD25hiFoxp3+ T cells have a predominant role in controlling autoimmune responses in normal individuals in a phenomenon known as physiological tolerance. It is probably an oversimplification, however, to infer that these cells play a role in the control of all other immune responses, especially since effective immune regulation is expected to last a lifetime. Because of thymic involution at the time of puberty, one would then have to postulate that all Tregs constitute a pool of self-perpetuating, long-term–surviving thymic emigrants. This appears unlikely, especially in humans.
Characteristics of adaptive Tregs in humans
It is this complex, though highly relevant, problem that Akbar’s group addresses in their study in this issue of the JCI (14). Akbar, Vukmanovic-Stejic, and colleagues present data showing that the proportion and functional integrity of CD4+CD25hiFoxp3+ Tregs are maintained in older (>70 years) human subjects and that these cells most probably do not derive from the thymic lineage of CD4+CD25hiFoxp3+ Tregs.
The authors used an original method based on the in vivo incorporation of deuterium-labeled glucose (or glucose derivatives) into the DNA of dividing cells, with ultimate follow-up of the labeled population and subsequent evaluation of cell replication and survival within phenotypically distinct peripheral T cell subsets (14). The results obtained convincingly show that throughout the individual’s whole life span, lymphocytes corresponding to the phenotypic and in vitro functional definition of Tregs are generated from the peripheral pool of CD4+CD45RO+CD25–Foxp3– memory T cells (Figure 1).
Figure 1
T lymphocytes originate from the thymus. Evidence has been accumulated to demonstrate that "natural" Tregs, whose major function is to control autoimmune responses, stem as a separate lineage in the thymus. These natural Tregs are CD4+, they express the transcription factor Foxp3, which represents a lineage marker, and high levels of CD25. Natural Tregs that migrate to the periphery keep their phenotypic and functional properties, which are essentially cytokine independent. In parallel, other subsets of CD4+ Tregs have been described that very effectively control immune responses not only to self antigens but also to a wide variety of nonself antigens (microbial, tumoral, and transplantation antigens). These Tregs are not present as such in the thymus; they derive from peripheral precursors that are CD4+CD25– and differentiate into functional Tregs following adequate stimulation (in the presence of the cognate antigen and specialized immunoregulatory cytokines, i.e., TGF-?, IL-10, and IL-4). They are generally termed "adaptive" Tregs. Once differentiated, adaptive Tregs, like natural Tregs, may express CD25 and Foxp3. However, one main feature that differentiates adaptive from natural Tregs is their unique cytokine dependence. The study by Vukmanovic-Stejic et al. in this issue of the JCI (14) proposes that, in humans, even at a very advanced age, adaptive Tregs essentially emerge from CD4+CD25– T cells belonging to the memory T cell pool (previously primed by cognate antigens). Presently, one cannot exclude, however, that especially in young adults, some adaptive Tregs may emerge from naive, peripheral CD4+CD25– T cells. Tr1, Treg type 1.
The distinction between "natural" Tregs of thymic origin and "adaptive" Tregs exclusively generated from peripheral CD25– lymphocytes following adequate conditions (including antigen stimulation and cytokine milieu) was suggested a few years ago from data obtained and validated in the mouse. It was then shown that peripheral CD25– T cells whose T cell receptor or coreceptors (e.g., CD4) are stimulated in the presence of TGF-? acquire regulatory properties that may be assessed both in vitro and in vivo (2, 4, 15, 16).
The results reported here by Vukmanovic-Stejic et al. (14) may represent the first indication of a similar dichotomy in human Tregs. If confirmed, 2 other sets of data are of particular interest, namely those showing that human Tregs have a shorter doubling time when compared with other subsets studied (e.g., peripheral classical memory and naive-type T cells) and that they appear particularly sensitive to apoptosis. Such observations may present a solid argument for the dependence of human adaptive Tregs on continuous antigen stimulation and/or the presence of growth factors in their immediate environment for their differentiation and survival. This could turn out to be an essential condition of their homeostasis.
Pending issues
These conclusions should be tempered, however, by an appreciation of the technical limitations of investigations performed in humans. The first concern is that the rationale of the work and its interpretations are based on the assumption that a high level of CD25 expression is a reliable marker for human Tregs. It is unquestionable that the CD4+CD25hi T cell subset concentrates both the majority of Foxp3+ cells and the essential part of functional regulatory capacity as assessed by in vitro coculture. However, how sure are we that these in vitro functional assays in humans reflect an in vivo regulatory functional capacity as shown in the mouse, using adoptive transfer experiments? Moreover, recent data suggest that the IL-7 receptor (CD127) is downregulated on a subset of human peripheral CD4+ T cells that are Foxp3+ and suppressive but that express no or low levels of CD25 (17). Additionally, one may consider whether Foxp3 in the human as opposed to the mouse is also expressed by activated T cells, independently of any regulatory function.
The second concern, closely linked to the first, is the critical issue of the antigen specificity of the Tregs studied, which is only very indirectly addressed (14). The results showing a biased T cell repertoire restricted to a given V? family (V?2 in this case) in a representative individual with persistent CMV infection are intriguing. However, the regulatory functional capacity of the CD4+CD25hiFoxp3+ cell subset detected in this V?2 anti-CMV population remains to be demonstrated.
To conclude, it appears plausible to extend to the human the dichotomy proposed in the mouse that distinguishes natural versus adaptive Tregs, which have distinct origins, namely, thymic-derived CD4+CD25+Foxp3+ cells in the case of natural regulatory lymphocytes versus peripheral memory–type CD4+CD25– precursors in the case of adaptive Tregs. In this context, it will be important to further experimentally dissect the adaptive Treg subset to more directly address whether or not the differences that have been proposed for each subset (e.g., Th2, Th3, Tr1, CD45RBlow T cells) in terms of phenotype and putative cytokine dependency are indeed a reflection of their belonging to distinct cell lineages.
References
Hori S., Takahashi T., Sakaguchi S.
2003. Control of autoimmunity by naturally arising regulatory CD4+ T cells. Adv. Immunol. 81:331–371.
Bach J.-F. 2003. Regulatory T cells under scrutiny. Nat. Rev. Immunol. 3:189–198.
Chatenoud L., Salomon B., Bluestone J.A. 2001. Suppressor T cells–they’re back and critical for regulation of autoimmunity! Immunol. Rev. 182:149–163.
Bluestone J.A. and Abbas A.K. 2003. Natural versus adaptive regulatory T cells. Nat. Rev. Immunol. 3:253–257.
Sakaguchi S. 2005. Naturally arising Foxp3-expressing CD25+CD4+ regulatory T cells in immunological tolerance to self and non-self. Nat. Immunol. 6:345–352.
Waldmann H., et al. 2006. Regulatory T cells in transplantation. Semin. Immunol. 18:111–119.
Coombes J.L., Robinson N.J., Maloy K.J., Uhlig H.H., Powrie F. 2005. Regulatory T cells and intestinal homeostasis. Immunol. Rev. 204:184–194.
Groux H., et al. 1997. A CD4+ T-cell subset inhibits antigen-specific T-cell responses and prevents colitis. Nature. 389:737–742.
Roncarolo M.G. and Levings M.K. 2000. The role of different subsets of T regulatory cells in controlling autoimmunity. Curr. Opin. Immunol. 12:676–683.
Levings M.K., et al. 2002. Human CD25+CD4+ T suppressor cell clones produce transforming growth factor beta, but not interleukin 10, and are distinct from type 1 T regulatory cells. J. Exp. Med. 196:1335–1346.
Weiner H.L., et al. 1994. Oral tolerance: immunologic mechanisms and treatment of animal and human organ-specific autoimmune diseases by oral administration of autoantigens. Annu. Rev. Immunol. 12:809–837.
Ochi H., et al. 2006. Oral CD3-specific antibody suppresses autoimmune encephalomyelitis by inducing CD4(+)CD25(-)LAP(+) T cells. Nat. Med. 12:627–635.
Tisch R., Wang B., Atkinson M.A., Serreze D.V., Friedline R. 2001. A glutamic acid decarboxylase 65-specific Th2 cell clone immunoregulates autoimmune diabetes in nonobese diabetic mice. J. Immunol. 166:6925–6936.
Vukmanovic-Stejic M., et al. 2006. Human CD4+ CD25hi Foxp3+ regulatory T cells are derived by rapid turnover of memory populations in vivo. J. Clin. Invest. 116:2423–2433 doi: 10.1172/JCI28941.
Chen W., et al. 2003. Conversion of peripheral CD4+CD25- naive T cells to CD4+CD25+ regulatory T cells by TGF-beta induction of transcription factor Foxp3. J. Exp. Med. 198:1875–1886.
Cobbold S.P., et al. 2004. Induction of foxP3+ regulatory T cells in the periphery of T cell receptor transgenic mice tolerized to transplants. J. Immunol. 172:6003–6010.
Liu W., et al. 2006. CD127 expression inversely correlates with FoxP3 and suppressive function of human CD4(+) T reg cells. J. Exp. Med. 203:1701–1711.