Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States.
Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.
Front Immunol. 2019 Jan 15;9:3064. doi: 10.3389/fimmu.2018.03064. eCollection 2018.
Memory B cells that are generated during an infection or following vaccination act as sentinels to guard against future infections. Upon repeat antigen exposure memory B cells differentiate into new antibody-secreting plasma cells to provide rapid and sustained protection. Some pathogens evade or suppress the humoral immune system, or induce memory B cells with a diminished ability to differentiate into new plasma cells. This leaves the host vulnerable to chronic or recurrent infections. Single cell approaches coupled with next generation antibody gene sequencing facilitate a detailed analysis of the pathogen-specific memory B cell repertoire. Monoclonal antibodies that are generated from antibody gene sequences allow a functional analysis of the repertoire. This review discusses what has been learned thus far from analysis of diverse pathogen-specific memory B cell compartments and describes major differences in their repertoires. Such information may illuminate ways to advance the goal of improving vaccine and therapeutic antibody design.
在感染或接种疫苗期间产生的记忆 B 细胞充当哨兵,以防止未来的感染。在重复抗原暴露后,记忆 B 细胞分化为新的抗体分泌浆细胞,以提供快速和持续的保护。一些病原体逃避或抑制体液免疫系统,或诱导记忆 B 细胞分化为新浆细胞的能力减弱。这使宿主容易受到慢性或复发性感染。单细胞方法结合下一代抗体基因测序,有助于对病原体特异性记忆 B 细胞库进行详细分析。从抗体基因序列中产生的单克隆抗体允许对库进行功能分析。这篇综述讨论了迄今为止从对各种病原体特异性记忆 B 细胞隔室的分析中学到的内容,并描述了它们库之间的主要差异。这些信息可能为如何推进提高疫苗和治疗性抗体设计的目标提供启示。