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Antigen-specific CD8+ T cell feedback activates NLRP3 inflammasome in antigen-presenting cells through perforin.

Yikun YaoSiyuan ChenMengtao CaoXing FanTao YangYin HuangXinyang SongYongqin LiLilin YeNan ShenYufang ShiXiaoxia LiFeng WangYoucun Qian
Published in: Nature communications (2017)
The connection between innate and adaptive immunity is best exemplified by antigen presentation. Although antigen-presenting cells (APCs) are required for antigen receptor-mediated T-cell activation, how T-cells feedback to APCs to sustain an antigen-specific immune response is not completely clear. Here we show that CD8+ T-cell (also called cytotoxic T lymphocytes, CTL) feedback activates the NLRP3 inflammasome in APCs in an antigen-dependent manner to promote IL-1β maturation. Perforin from antigen-specific CTLs is required for NLRP3 inflammasome activation in APCs. Furthermore, such activation of NLRP3 inflammasome contributes to the induction of antigen-specific antitumour immunity and pathogenesis of graft-versus-host diseases. Our study reveals a positive feedback loop between antigen-specific CTLs and APC to amplify adaptive immunity.
Keyphrases
  • nlrp inflammasome
  • immune response
  • induced apoptosis
  • cell cycle arrest
  • case report
  • transcription factor
  • signaling pathway
  • endoplasmic reticulum stress
  • cell death
  • cell proliferation