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Immune tolerance. Regulatory T cells generated early in life play a distinct role in maintaining self-tolerance.


ABSTRACT: Aire is an important regulator of immunological tolerance, operating in a minute subset of thymic stromal cells to induce transcripts encoding peptides that guide T cell selection. Expression of Aire during a perinatal age window is necessary and sufficient to prevent the multiorgan autoimmunity characteristic of Aire-deficient mice. We report that Aire promotes the perinatal generation of a distinct compartment of Foxp3(+)CD4(+) regulatory T (Treg) cells, which stably persists in adult mice. This population has a role in maintaining self-tolerance, a transcriptome and an activation profile distinguishable from those of Tregs produced in adults. Underlying the distinct Treg populations are age-dependent, Aire-independent differences in the processing and presentation of thymic stromal-cell peptides, resulting in different T cell receptor repertoires. Our findings expand the notion of a developmentally layered immune system.

SUBMITTER: Yang S 

PROVIDER: S-EPMC4710357 | biostudies-literature | 2015 May

REPOSITORIES: biostudies-literature

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Immune tolerance. Regulatory T cells generated early in life play a distinct role in maintaining self-tolerance.

Yang Siyoung S   Fujikado Noriyuki N   Kolodin Dmitriy D   Benoist Christophe C   Mathis Diane D  

Science (New York, N.Y.) 20150319 6234


Aire is an important regulator of immunological tolerance, operating in a minute subset of thymic stromal cells to induce transcripts encoding peptides that guide T cell selection. Expression of Aire during a perinatal age window is necessary and sufficient to prevent the multiorgan autoimmunity characteristic of Aire-deficient mice. We report that Aire promotes the perinatal generation of a distinct compartment of Foxp3(+)CD4(+) regulatory T (Treg) cells, which stably persists in adult mice. Th  ...[more]

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