| Title | Antibody modulation of B cell responses-Incorporating positive and negative feedback. |
| Publication Type | Journal Article |
| Year of Publication | 2024 |
| Authors | Cyster JG, Wilson PC |
| Journal | Immunity |
| Volume | 57 |
| Issue | 7 |
| Pagination | 1466-1481 |
| Date Published | 2024 Jul 09 |
| ISSN | 1097-4180 |
| Keywords | Animals, Antibodies, Viral, Antibody Formation, B-Lymphocytes, COVID-19, Feedback, Physiological, Humans, Immunity, Humoral, Mice, Receptors, Fc, SARS-CoV-2 |
| 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. |
| DOI | 10.1016/j.immuni.2024.06.009 |
| Custom 1 | |
| Alternate Journal | Immunity |
| PubMed ID | 38986442 |
| PubMed Central ID | PMC11257158 |
| Grant List | 75N93019C00051 / AI / NIAID NIH HHS / United States R01 AI040098 / AI / NIAID NIH HHS / United States R37 AI040098 / AI / NIAID NIH HHS / United States |
