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Antibody modulation of B cell responses-Incorporating positive and negative feedback.
Cyster, Jason G; Wilson, Patrick C.
Affiliation
  • Cyster JG; Howard Hughes Medical Institute and Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: jason.cyster@ucsf.edu.
  • Wilson PC; Drukier Institute for Children's Health, Department of Pediatrics, Weill Cornell Medicine, New York, NY, USA. Electronic address: pcw4001@med.cornell.edu.
Immunity ; 57(7): 1466-1481, 2024 Jul 09.
Article in En | MEDLINE | ID: mdl-38986442
ABSTRACT
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: B-Lymphocytes / SARS-CoV-2 / COVID-19 Limits: Animals / Humans Language: En Journal: Immunity Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: B-Lymphocytes / SARS-CoV-2 / COVID-19 Limits: Animals / Humans Language: En Journal: Immunity Year: 2024 Document type: Article