Spatiotemporal regulation of peripheral T cell tolerance
Author(s) -
Chrysothemis C. Brown,
Alexander Y. Rudensky
Publication year - 2023
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.adg6425
Subject(s) - peripheral tolerance , biology , immune tolerance , self tolerance , effector , immune system , central tolerance , immunology , function (biology) , antigen , oral tolerance , immunologic tolerance , t cell , microbiology and biotechnology , holobiont , clonal deletion , genetics , t cell receptor , bacteria , symbiosis
The incomplete removal of T cells that are reactive against self-proteins during their differentiation in the thymus requires mechanisms of tolerance that prevent their effector function within the periphery. A further challenge is imposed by the need to establish tolerance to the holobiont self, which comprises a highly complex community of commensal microorganisms. Here, we review recent advances in the investigation of peripheral T cell tolerance, focusing on new insights into mechanisms of tolerance to the gut microbiota, including tolerogenic antigen-presenting cell types and immunomodulatory lymphocytes, and their layered ontogeny that underlies developmental windows for establishing intestinal tolerance. While emphasizing the intestine as a model tissue for studying peripheral T cell tolerance, we highlight overlapping and distinct pathways that underlie tolerance to self-antigens versus commensal antigens within a broader framework for immune tolerance.
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