Transcriptional regulation of B cell class-switch recombination: the role in development of noninfectious complications

被引:4
作者
Vlachiotis, Stelios [1 ]
Abolhassani, Hassan [1 ,2 ]
机构
[1] Karolinska Inst, Dept Biosci & Nutr, Huddinge, Sweden
[2] Univ Tehran Med Sci, Res Ctr Immunodeficiencies, Pediat Ctr Excellence, Childrens Med Ctr, Tehran, Iran
关键词
Primary immunodeficiency; inborn errors of immunity; humoral immunity; B cell; class switch recombination; cytokines; transcription factors; ACTIVATION-INDUCED DEAMINASE; INDUCED CYTIDINE DEAMINASE; RNA-POLYMERASE-II; HUMAN NAIVE; PLASMA-CELL; DNA RECOMBINATION; HISTONE MODIFICATION; CLINICAL PHENOTYPE; DOWN-REGULATION; AID EXPRESSION;
D O I
10.1080/1744666X.2022.2123795
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction The process of immunoglobulin class switch recombination (CSR) occurs in secondary lymphoid organs. This highly regulated process is essential for the development of different antibody isotype maturation and long-life memory/plasma cell generation. Patients with impaired CSR present heterogeneous noninfectious complications. Areas covered We provide an overview of recent advancements in the tight regulation of B cells before and during the CSR at different levels of cytokine stimulations, intracellular signaling, transcription-factor activation, gene transcription, and epigenetic controls. Expert opinion Besides recurrent infections which result from the lack of production of class-switched immunoglobulins, intrinsic B cell signaling pathways and regulatory component defects have distinct roles in other immune-related clinical manifestations including autoimmunity, atopy, lymphoproliferation, and cancer.
引用
收藏
页码:1145 / 1154
页数:10
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