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OX40 signaling favors the induction of T(H)9 cells and airway inflammation.

Xiang Xiao | Savithri Balasubramanian | Wentao Liu | Xiufeng Chu | Haibin Wang | Elizabeth J Taparowsky | Yang-Xin Fu | Yongwon Choi | Matthew C Walsh | Xian Chang Li
Nature immunology | 2012

The mechanisms that regulate the T(H)9 subset of helper T cells and diseases mediated by T(H)9 cells remain poorly defined. Here we found that the costimulatory receptor OX40 was a powerful inducer of T(H)9 cells in vitro and T(H)9 cell-dependent airway inflammation in vivo. In polarizing conditions based on transforming growth factor-β (TGF-β), ligation of OX40 inhibited the production of induced regulatory T cells and the T(H)17 subset of helper T cells and diverted CD4(+)Foxp3(-) T cells to a T(H)9 phenotype. Mechanistically, OX40 activated the ubiquitin ligase TRAF6, which triggered induction of the kinase NIK in CD4(+) T cells and the noncanonical transcription factor NF-κB pathway; this subsequently led to the generation of T(H)9 cells. Thus, our study identifies a previously unknown mechanism for the induction of T(H)9 cells and may have important clinical implications in allergic inflammation.

Pubmed ID: 22842344

Research resources used in this publication

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Associated grants

  • Agency: NIAID NIH HHS, United States
    Id: R01 AI064909
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI070315
  • Agency: NIAID NIH HHS, United States
    Id: R56 AI070315

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