A distinct subpopulation of CD25−T-follicular regulatory cells localizes in the germinal centers
Author(s) -
James B. Wing,
Yohko Kitagawa,
Michela Locci,
Hannah Hume,
Christopher Tay,
Takayoshi Morita,
Yujiro Kidani,
K. Matsuda,
Takeshi Inoue,
Tomohiro Kurosaki,
Shane Crotty,
Cevayir Coban,
Naganari Ohkura,
Shimon Sakaguchi
Publication year - 2017
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1705551114
Subject(s) - bcl6 , germinal center , il 2 receptor , cxcr5 , foxp3 , interleukin 21 , transcription factor , biology , microbiology and biotechnology , effector , follicular phase , antibody , immunology , gene , t cell , b cell , immune system , genetics
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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