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Thymic self-reactivity selects natural interleukin 17-producing T cells that can regulate peripheral inflammation.


ABSTRACT: Interleukin 17 (IL-17)-producing CD4(+) helper T cells (T(H)-17 cells) share a developmental relationship with Foxp3(+) regulatory T cells (T(reg) cells). Here we show that a T(H)-17 population differentiates in the thymus in a manner influenced by recognition of self antigen and by the cytokines IL-6 and transforming growth factor-beta (TGF-beta). Like previously described T(H)-17 cells, the T(H)-17 cells that developed in the thymus expressed the transcription factor RORgamma t and the IL-23 receptor. These cells also expressed alpha(4)beta(1) integrins and the chemokine receptor CCR6 and were recruited to the lung, gut and liver. In the liver, these cells secreted IL-22 in response to self antigen and mediated host protection during inflammation. Thus, T(H)-17 cells, like T(reg) cells, can be selected by self antigens in the thymus.

SUBMITTER: Marks BR 

PROVIDER: S-EPMC2751862 | biostudies-literature | 2009 Oct

REPOSITORIES: biostudies-literature

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Thymic self-reactivity selects natural interleukin 17-producing T cells that can regulate peripheral inflammation.

Marks Benjamin R BR   Nowyhed Heba N HN   Choi Jin-Young JY   Poholek Amanda C AC   Odegard Jared M JM   Flavell Richard A RA   Craft Joe J  

Nature immunology 20090906 10


Interleukin 17 (IL-17)-producing CD4(+) helper T cells (T(H)-17 cells) share a developmental relationship with Foxp3(+) regulatory T cells (T(reg) cells). Here we show that a T(H)-17 population differentiates in the thymus in a manner influenced by recognition of self antigen and by the cytokines IL-6 and transforming growth factor-beta (TGF-beta). Like previously described T(H)-17 cells, the T(H)-17 cells that developed in the thymus expressed the transcription factor RORgamma t and the IL-23 r  ...[more]

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