4.7 Article

IL-1β and IL-2 convert human Treg into TH17 cells

期刊

CLINICAL IMMUNOLOGY
卷 131, 期 2, 页码 298-307

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.clim.2008.12.008

关键词

Treg; T(H)17; IL-1 beta; IL-2

资金

  1. Ludwig Institute for Cancer Research (USA)
  2. Cancer Research Institute (USA)
  3. Institut National de la Sante et de la Recherche Medicale (France)
  4. Institut National du Cancer (France)
  5. Conseil Regional des Pays de (a Loire (France)
  6. European Structural Funds (FEDER program)

向作者/读者索取更多资源

Natural CD4(+)CD25(+) regulatory T cells (Treg) and interleukin 17 (IL-17)-producing T helper cells (T(H)17) carry out opposite functions, the former maintaining self-tolerance and the latter being involved in inflammation and autoimmunity. We report here that stimulation of human Natural Treg under T(H)17 polarizing conditions in the presence of IL-2 converts them into T(H)17 cells. Conversion of Tregs into T(H)17 cells occurs both from natural naive Tregs (NnTregs) and, to a higher extent, from memory Tregs (MTregs). Among antigen presenting cells, fresh monocytes activated by microbial stimuli were the most efficient inducers of T(H)17 cells from Tregs. Conversion of Treg into T(H)17 cells was induced by IL-1 beta and involved down-regulation of the Treg lineage transcription factor FOXP3 and suppressive functions. Our results indicate that, under inflammatory conditions, in the presence of IL-2, Treg can be converted into pro-inflammatory T(H)17 cells and establish a functional link between inflammation and autoimmunity. (C) 2009 Elsevier Inc. All. rights reserved.

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