Interaction between B7-H1 and PD-1 determines initiation and reversal of T-cell anergy.

نویسندگان

  • Fumihiko Tsushima
  • Sheng Yao
  • Tahiro Shin
  • Andrew Flies
  • Sarah Flies
  • Haiying Xu
  • Koji Tamada
  • Drew M Pardoll
  • Lieping Chen
چکیده

Although self-reactive T-cell precursors can be eliminated upon recognition of self-antigen presented in the thymus, this central tolerance process is often incomplete, and additional mechanisms are required to prevent autoimmunity. Recent studies indicates that the interaction between B7-H1 and its receptor PD-1 on activated T cells plays an important role in the inhibition of T-cell responses in peripheral organs. Here, we show that, before their exit to the periphery, T cells in lymphoid organs rapidly up-regulate PD-1 upon tolerogen recognition. Ablation of the B7-H1 and PD-1 interaction when T cells are still in lymphoid organs prevents anergy. Furthermore, blockade of B7-H1 and PD-1 interaction could render anergic T cells responsive to antigen. Our results thus reveal previously unappreciated roles of B7-H1 and PD-1 interaction in the control of initiation and reversion of T-cell anergy.

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IMMUNOBIOLOGY Interaction between B7-H1 and PD-1 determines initiation and reversal of T-cell anergy

Although self-reactive T-cell precursors can be eliminated upon recognition of self-antigen presented in the thymus, this central tolerance process is often incomplete, and additional mechanisms are required to prevent autoimmunity. Recent studies indicates that the interaction between B7-H1 and its receptor PD-1 on activated T cells plays an important role in the inhibition of T-cell responses...

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عنوان ژورنال:
  • Blood

دوره 110 1  شماره 

صفحات  -

تاریخ انتشار 2007