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A distinct subpopulation of CD25- T-follicular regulatory cells localizes in the germinal centers.

James Badger WingYohko KitagawaMichela LocciHannah HumeChristopher TayTakayoshi MoritaYujiro KidaniKyoko MatsudaTakeshi InoueTomohiro KurosakiShane CrottyCevayir CobanNaganari OhkuraShimon Sakaguchi
Published in: Proceedings of the National Academy of Sciences of the United States of America (2017)
T-follicular helper (Tfh) cells differentiate through a multistep process, culminating in germinal center (GC) localized GC-Tfh cells that provide support to GC-B cells. T-follicular regulatory (Tfr) cells have critical roles in the control of Tfh cells and GC formation. Although Tfh-cell differentiation is inhibited by IL-2, regulatory T (Treg) cell differentiation and survival depend on it. Here, we describe a CD25- subpopulation within both murine and human PD1+CXCR5+Foxp3+ Tfr cells. It is preferentially located in the GC and can be clearly differentiated from CD25+ non-GC-Tfr, Tfh, and effector Treg (eTreg) cells by the expression of a wide range of molecules. In comparison to CD25+ Tfr and eTreg cells, CD25- Tfr cells partially down-regulate IL-2-dependent canonical Treg features, but retain suppressive function, while simultaneously up-regulating genes associated with Tfh and GC-Tfh cells. We suggest that, similar to Tfh cells, Tfr cells follow a differentiation pathway generating a mature GC-localized subpopulation, CD25- Tfr cells.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • endoplasmic reticulum stress
  • signaling pathway
  • oxidative stress
  • cell death
  • mass spectrometry
  • poor prognosis
  • regulatory t cells
  • immune response