| Literature DB >> 28756897 |
Jodi L Karnell1, Varsha Kumar1, Jingya Wang1, Shu Wang1, Elisaveta Voynova1, Rachel Ettinger2.
Abstract
A growing body of evidence suggests that when B cells are chronically stimulated, a phenotypically unique subset expands. Data suggest that this atypical population contains B cell receptor (BCR) specificities capable of binding the antigen, or sets of antigens that initiated the expansion of these cells. These B cells have been given various names, including double negative B cells, atypical memory B cells, tissue-like memory B cells, or age associated B cells (ABCs). However, on close inspection these reports described B cell subsets that closely resemble B cells we refer to as CD11c+ B cells that often express T-bet. Here we will review the human studies that describe atypical memory B cells and compare and contrast their phenotype and suggested function in health and disease.Entities:
Keywords: ABCs; Autoimmunity; B cells; CD11c; Infection; T-bet
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Year: 2017 PMID: 28756897 DOI: 10.1016/j.cellimm.2017.05.008
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868