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Follicular regulatory T cells: a novel target for immunotherapy?

Yao HuangZhe ChenHui WangXin BaPan ShenWeiji LinYu WangKai QinYing HuangSheng-Hao Tu
Published in: Clinical & translational immunology (2020)
High-affinity antibodies are produced during multiple processes in germinal centres (GCs), where follicular helper T (Tfh) cells interact closely with B cells to support B-cell survival, differentiation and proliferation. Recent studies have revealed that a specialised subset of regulatory T cells, follicular regulatory T (Tfr) cells, especially fine-tune Tfh cells and GC B cells, ultimately regulating GC reactions. Alterations in frequencies or function of Tfr cells may result in multiple autoantibody-mediated or autoantibody-associated diseases. This review discusses recent insights into the physiology and pathology of Tfr cells, with a special emphasis on their potential roles in human diseases. Discrepancies are common among studies, reflecting the limited understanding of Tfr cells. Further exploration of the mechanisms of Tfr cells in these diseases and thus targeting Tfr cells may help reinstate immune homeostasis and provide novel immunotherapy.
Keyphrases
  • induced apoptosis
  • regulatory t cells
  • cell cycle arrest
  • signaling pathway
  • cell death
  • dendritic cells
  • transcription factor
  • cell proliferation
  • air pollution
  • single cell
  • high resolution
  • risk assessment