4.7 Article

A dominant function for interleukin 27 in generating interleukin 10-producing anti-inflammatory T cells

期刊

NATURE IMMUNOLOGY
卷 8, 期 12, 页码 1380-1389

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NATURE PUBLISHING GROUP
DOI: 10.1038/ni1541

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资金

  1. NIAID NIH HHS [R01 AI073542-01, R01 AI073542, R01AI073542-01, AI043458] Funding Source: Medline
  2. NINDS NIH HHS [1R01NS046414, 2R01NS35685-06, 1P01NS38037-04, 2R37NS30843-11, 1R01NS045937-01, NS038037, R01 NS059996] Funding Source: Medline
  3. PHS HHS [2P01A139671-07, 1R01A144880-03] Funding Source: Medline

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Regulatory T cells (T-reg cells) expressing the transcription factor Foxp3 are key in maintaining the balance of immune homeostasis. However, distinct induced T regulatory type 1 ( Tr1) cells that lack Foxp3 expression also regulate T cell function, mainly by producing the immunosuppressive cytokine interleukin 10 (IL-10). However, the factors required for the induction of IL-10-producing suppressive T cells are not fully understood. Here we demonstrate that dendritic cells modified by Treg cells induced the generation of IL-10-producing Tr1 cells. The differentiation of naive CD4(+) T cells into IL-10-producing cells was mediated by IL-27 produced by the T-reg cell-modified dendritic cells, and transforming growth factor-beta amplified the generation of induced IL-10(+) Tr1 cells by IL-27. Thus, IL-27 and transforming growth factor-beta promote the generation of IL-10-producing Tr1 cells.

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