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Reciprocal regulation of T follicular helper cells and dendritic cells drives colitis development.

Xue BaiSijie ChenXinxin ChiBowen XieXinyi GuoHan FengPeng WeiDi ZhangShan XieTian XieYongzhen ChenMengting GouQin QiaoXinwei LiuWei JinWei XuZixuan ZhaoQi XingXiaohu WangXuegong ZhangChen Dong
Published in: Nature immunology (2024)
The immunological mechanisms underlying chronic colitis are poorly understood. T follicular helper (T FH ) cells are critical in helping B cells during germinal center reactions. In a T cell transfer colitis model, a lymphoid structure composed of mature dendritic cells (DCs) and T FH cells was found within T cell zones of colonic lymphoid follicles. T FH cells were required for mature DC accumulation, the formation of DC-T cell clusters and colitis development. Moreover, DCs promoted T FH cell differentiation, contributing to colitis development. A lineage-tracing analysis showed that, following migration to the lamina propria, T FH cells transdifferentiated into long-lived pathogenic T H 1 cells, promoting colitis development. Our findings have therefore demonstrated the reciprocal regulation of T FH cells and DCs in colonic lymphoid follicles, which is critical in chronic colitis pathogenesis.
Keyphrases
  • induced apoptosis
  • dendritic cells
  • cell cycle arrest
  • endoplasmic reticulum stress
  • ulcerative colitis
  • regulatory t cells
  • oxidative stress