Author:
Zhong Ziwen,Nan Ke,Weng Meilin,Yue Ying,Zhou Wenchang,Wang Zhiqiang,Chu Yiwei,Liu Ronghua,Miao Changhong
Abstract
B cells are well known as key mediators of humoral immune responses via the production of antibodies. Immunoglobulin A (IgA) is the most abundantly produced antibody isotype and provides the first line of immune protection at mucosal surfaces. However, IgA has long been a divisive molecule with respect to tumor progression. IgA exerts anti- or pro-tumor effect in different tumor types. In this review, we summarize emerging evidence regarding the production and effects of IgA and IgA+ cells in the tumor microenvironment (TME). Moreover, we discuss that the TME cytokines, host diet, microbiome, and metabolites play a pivotal role in controlling the class-switch recombination (CSR) of IgA. The analysis of intratumoral Ig repertoires and determination of metabolites that influence CSR may help establish novel therapeutic targets for the treatment of cancers.
Funder
Shanghai Rising-Star Program
National Natural Science Foundation of China
National Science and Technology Major Project
Subject
Immunology,Immunology and Allergy
Cited by
14 articles.
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