Howard Hughes Medical Institute and Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA, USA.
Drukier Institute for Children's Health, Department of Pediatrics, Weill Cornell Medicine, New York, NY, USA.
Immunity. 2024 Jul 9;57(7):1466-1481. doi: 10.1016/j.immuni.2024.06.009.
Antibodies are powerful modulators of ongoing and future B cell responses. While the concept of antibody feedback has been appreciated for over a century, the topic has seen a surge in interest due to the evidence that the broadening of antibody responses to SARS-CoV-2 after a third mRNA vaccination is a consequence of antibody feedback. Moreover, the discovery that slow antigen delivery can lead to more robust humoral immunity has put a spotlight on the capacity for early antibodies to augment B cell responses. Here, we review the mechanisms whereby antibody feedback shapes B cell responses, integrating findings in humans and in mouse models. We consider the major influence of epitope masking and the diverse actions of complement and Fc receptors and provide a framework for conceptualizing the ways antigen-specific antibodies may influence B cell responses to any form of antigen, in conditions as diverse as infectious disease, autoimmunity, and cancer.
抗体是调节正在进行和未来 B 细胞反应的强大调节剂。尽管抗体反馈的概念已经存在了一个多世纪,但由于证据表明,第三次 mRNA 疫苗接种后对 SARS-CoV-2 的抗体反应的扩大是抗体反馈的结果,因此该主题的兴趣大增。此外,发现缓慢的抗原递呈会导致更强大的体液免疫,这使得人们关注早期抗体增强 B 细胞反应的能力。在这里,我们综述了抗体反馈调节 B 细胞反应的机制,整合了人类和小鼠模型中的发现。我们考虑了表位掩蔽的主要影响以及补体和 Fc 受体的多种作用,并为概念化抗原特异性抗体可能影响任何形式的抗原的 B 细胞反应的方式提供了一个框架,包括传染病、自身免疫和癌症等各种情况下。