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

نویسندگان

  • James Badger Wing
  • Yohko Kitagawa
  • Michela Locci
  • Hannah Hume
  • Christopher Tay
  • Takayoshi Morita
  • Yujiro Kidani
  • Kyoko Matsuda
  • Takeshi Inoue
  • Tomohiro Kurosaki
  • Shane Crotty
  • Cevayir Coban
  • Naganari Ohkura
  • Shimon Sakaguchi
چکیده

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.

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عنوان ژورنال:
  • Proceedings of the National Academy of Sciences of the United States of America

دوره 114 31  شماره 

صفحات  -

تاریخ انتشار 2017