| Literature DB >> 28698369 |
James Badger Wing1, Yohko Kitagawa1, Michela Locci2, Hannah Hume1, Christopher Tay1, Takayoshi Morita1, Yujiro Kidani1, Kyoko Matsuda3, Takeshi Inoue4, Tomohiro Kurosaki4,5, Shane Crotty2, Cevayir Coban3, Naganari Ohkura1, Shimon Sakaguchi6,7.
Abstract
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.Entities:
Keywords: T-follicular regulatory cell; Tfh cell; Tfr cell; Treg cell; germinal center
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Year: 2017 PMID: 28698369 PMCID: PMC5547636 DOI: 10.1073/pnas.1705551114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205