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Journal ArticleDOI

Naturally Arising CD4+ Regulatory T Cells for Immunologic Self-Tolerance and Negative Control of Immune Responses

Shimon Sakaguchi
- 19 Mar 2004 - 
- Vol. 22, Iss: 1, pp 531-562
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TLDR
How naturally arising CD25+CD4+ regulatory T cells contribute to the maintenance of immunologic self-tolerance and negative control of various immune responses, and how they can be exploited to prevent and treat autoimmune disease, allergy, cancer, and chronic infection, or establish donor-specific transplantation tolerance are discussed.
Abstract
▪ Abstract Naturally occurring CD4+ regulatory T cells, the majority of which express CD25, are engaged in dominant control of self-reactive T cells, contributing to the maintenance of immunologic self-tolerance. Their depletion or functional alteration leads to the development of autoimmune disease in otherwise normal animals. The majority, if not all, of such CD25+CD4+ regulatory T cells are produced by the normal thymus as a functionally distinct and mature subpopulation of T cells. Their repertoire of antigen specificities is as broad as that of naive T cells, and they are capable of recognizing both self and nonself antigens, thus enabling them to control various immune responses. In addition to antigen recognition, signals through various accessory molecules and via cytokines control their activation, expansion, and survival, and tune their suppressive activity. Furthermore, the generation of CD25+CD4+ regulatory T cells in the immune system is at least in part developmentally and genetically contro...

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Citations
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Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells.

TL;DR: It is shown that IL-6, an acute phase protein induced during inflammation, completely inhibits the generation of Foxp3+ Treg cells induced by TGF-β, and the data demonstrate a dichotomy in thegeneration of pathogenic (TH17) T cells that induce autoimmunity and regulatory (Foxp3+) T Cells that inhibit autoimmune tissue injury.
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Naturally arising Foxp3-expressing CD25+CD4+ regulatory T cells in immunological tolerance to self and non-self.

TL;DR: Naturally arising CD25+CD4+ regulatory T cells actively maintain immunological self-tolerance, and are a good target for designing ways to induce or abrogate immunological tolerance to self and non-self antigens.
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Transforming growth factor-beta regulation of immune responses.

TL;DR: This review highlights the findings that have advanced the understanding of TGF-beta in the immune system and in disease.
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A function for interleukin 2 in Foxp3-expressing regulatory T cells

TL;DR: Gene expression analysis showed that IL-2 signaling was required for maintenance of the expression of genes involved in the regulation of cell growth and metabolism, which seems to be critically required for maintaining the homeostasis and competitive fitness of Treg cells in vivo.
References
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Journal ArticleDOI

Human CD25+CD4+ T Suppressor Cell Clones Produce Transforming Growth Factor β, but not Interleukin 10, and Are Distinct from Type 1 T Regulatory Cells

TL;DR: It is demonstrated at the clonal level that Tr1 and CD25+CD4+ T cells are two distinct subsets of regulatory cells with different cytokine production profiles, which indicates that naturally occurring human CD25–CD4–T cells are distinct from IL-10–producing Tr1 cells.
Journal ArticleDOI

Origin of major histocompatibility complex polymorphism: the trans-species hypothesis.

TL;DR: The sphinx of immunology, the major histocompatibility complex (MHC), has revealed most of her secrets except the two most profound ones: what is the true MHC function, andWhat is the origin and significance of MHC polymorphism?
Journal ArticleDOI

Generation of Anergic and Potentially Immunoregulatory CD25+CD4 T Cells In Vivo After Induction of Peripheral Tolerance with Intravenous or Oral Antigen

TL;DR: The DO11.10 TCR transgenic adoptive transfer system was used to show that cells of similar phenotype may also arise in the course of peripheral tolerance induction, and emerged within 1 wk following Ag exposure and correlated negatively with the number of initial cell divisions.
Journal ArticleDOI

Major Histocompatibility Complex Class II–Positive Cortical Epithelium Mediates the Selection of Cd4+25+ Immunoregulatory T Cells

TL;DR: It is found that CD4+25+ T cells are present in the thymus and periphery of K14-Aβ b and H2-DMα–deficient mice and, like their wild-type counterparts, suppress the proliferation of cocultured CD4-25− effector T cells.
Journal ArticleDOI

In vivo dynamics of antigen-specific regulatory T cells not predicted from behavior in vitro.

TL;DR: It is found that regulatory T cells maintained their phenotype in the absence of antigen, were not anergic in vivo, and proliferated as extensively as naive CD4+ T cells after immunization without losing their suppressive function in vivo and in vitro.
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