| Literature DB >> 25609381 |
Adnan R Khan1, Emily Hams1, Achilleas Floudas1, Tim Sparwasser2, Casey T Weaver3, Padraic G Fallon4.
Abstract
Specific B-cell subsets can regulate T-cell immune responses, and are termed regulatory B cells (Breg). The majority of Breg cells described in mouse and man have been identified by IL-10 production and are known to suppress allergy and autoimmunity. However, Breg cell mediated immune suppression, independent of IL-10, also occurs. Here we show that Breg cells play a critical role in regulating humoral immunity mediated by CD4(+)CXCR5(+)PD-1(+) follicular helper T cells, and can suppress inflammation in autoimmune disease through elevated expression of PD-L1. We have also identified that these B cells are resistant to αCD20 B-cell depletion. This work describes how Breg cells are critical in humoral homoeostasis and may have implications for the regulation of autoimmune diseases.Entities:
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Year: 2015 PMID: 25609381 DOI: 10.1038/ncomms6997
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919