B-Cell Memory Responses to Variant Viral Antigens

被引:9
|
作者
White, Harry N. [1 ]
机构
[1] Univ Exeter, Dept Biosci, Geoffrey Pope Bldg,Stocker Rd, Exeter EX4 4QD, Devon, England
来源
VIRUSES-BASEL | 2021年 / 13卷 / 04期
关键词
virus mutation; antibody; immune memory; vaccine; dengue; influenza; coronavirus; ANTIBODY-DEPENDENT ENHANCEMENT; DENGUE VIRUS-INFECTION; GERMINAL-CENTER; CROSS-REACTIVITY; DOMAIN-III; BINDING; IMMUNODOMINANCE; DIVERSITY; SELECTION; RNA;
D O I
10.3390/v13040565
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A central feature of vertebrate immune systems is the ability to form antigen-specific immune memory in response to microbial challenge and so provide protection against future infection. In conflict with this process is the ability that many viruses have to mutate their antigens to escape infection- or vaccine-induced antibody memory responses. Mutable viruses such as dengue virus, influenza virus and of course coronavirus have a major global health impact, exacerbated by this ability to evade immune responses through mutation. There have been several outstanding recent studies on B-cell memory that also shed light on the potential and limitations of antibody memory to protect against viral antigen variation, and so promise to inform new strategies for vaccine design. For the purposes of this review, the current understanding of the different memory B-cell (MBC) populations, and their potential to recognize mutant antigens, will be described prior to some examples from antibody responses against the highly mutable RNA based flaviviruses, influenza virus and SARS-CoV-2.
引用
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页数:11
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