<p>The aberrant accumulation of intracellular disulfides promotes cancer cell disulfidptosis; however, how disulfide stress influences tumour-infiltrating CD8<sup>+</sup> T cell function remains unknown. Here we demonstrate that lactate dehydrogenase B (LDHB) facilitates intratumoural CD8<sup>+</sup> T cell disulfidptosis and exhaustion, leading to impaired antitumour immunity. SLC7A11-mediated cystine uptake by CD8<sup>+</sup> T cells induces disulfidptosis, which plays critical roles in the development of exhausted CD8<sup>+</sup> T cells. LDHB restricts glucose-6-phosphate dehydrogenase (G6PD) activity in exhausted CD8<sup>+</sup> T cells by interacting with G6PD, causing NADPH depletion and consequently triggering disulfidptosis. Accordingly, the loss of LDHB in T cells prevents disulfidptosis-dependent CD8<sup>+</sup> T cell exhaustion and improves antitumour immunity. Mechanistically, STAT3 directs LDHB expression to limit G6PD activity and mediate disulfidptosis in exhausted CD8<sup>+</sup> T cells. Our results highlight the distinct roles of disulfidptosis and ferroptosis in driving CD8<sup>+</sup> T cell exhaustion and suggest a potential therapeutic strategy to target LDHB in cancer immunotherapy.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Lactate dehydrogenase B facilitates disulfidptosis and exhaustion of tumour-infiltrating CD8+ T cells

  • Jie Wan,
  • Jian-Hong Shi,
  • Min Shi,
  • Haiyan Huang,
  • Zhen Zhang,
  • Wenyan Li,
  • Chenyue Guo,
  • Rujuan Bao,
  • Xiaoyan Yu,
  • Qiaoqiao Han,
  • Xian Du,
  • Song Li,
  • Youqiong Ye,
  • Xingang Cui,
  • Xia Li,
  • Jing-Hua Li,
  • Qiang Zou

摘要

The aberrant accumulation of intracellular disulfides promotes cancer cell disulfidptosis; however, how disulfide stress influences tumour-infiltrating CD8+ T cell function remains unknown. Here we demonstrate that lactate dehydrogenase B (LDHB) facilitates intratumoural CD8+ T cell disulfidptosis and exhaustion, leading to impaired antitumour immunity. SLC7A11-mediated cystine uptake by CD8+ T cells induces disulfidptosis, which plays critical roles in the development of exhausted CD8+ T cells. LDHB restricts glucose-6-phosphate dehydrogenase (G6PD) activity in exhausted CD8+ T cells by interacting with G6PD, causing NADPH depletion and consequently triggering disulfidptosis. Accordingly, the loss of LDHB in T cells prevents disulfidptosis-dependent CD8+ T cell exhaustion and improves antitumour immunity. Mechanistically, STAT3 directs LDHB expression to limit G6PD activity and mediate disulfidptosis in exhausted CD8+ T cells. Our results highlight the distinct roles of disulfidptosis and ferroptosis in driving CD8+ T cell exhaustion and suggest a potential therapeutic strategy to target LDHB in cancer immunotherapy.