| Literature DB >> 26004919 |
Xiangjun Chen1, Gen Li2, Zhengpeng Wan2, Ce Liu2, Yingyue Zeng2, Wanli Liu3.
Abstract
Antibody memory is critical for protection against many human infectious diseases and is the basis for nearly all current human vaccines. Isotype switched immunoglobulin (Ig) G-expressing memory B cells are considered as one of the fundaments for the rapid, high affinity and high-titered memory antibody response. The detailed molecular mechanism of the enhanced activation of IgG-switched memory B cells upon BCR engagement with antigens has been an elusive question in immunology. In this review, we tried to discuss all the exciting new advances revealing the molecular mechanisms of the transmembrane signaling through mIgG cytoplasmic tail in IgG-switched memory B cells.Entities:
Keywords: B cell receptor; CD22; Grb2; Memory B cell; SAP97; mIgG cytoplasmic tail
Mesh:
Substances:
Year: 2015 PMID: 26004919 DOI: 10.1016/j.pbiomolbio.2015.04.010
Source DB: PubMed Journal: Prog Biophys Mol Biol ISSN: 0079-6107 Impact factor: 3.667