Multiple layers of B cell memory with different effector functions
Abstract
Memory B cells are at the center of longstanding controversies regarding the presence of antigen for their survival and their re-engagement in germinal centers after secondary challenge. Using a new mouse model of memory B cell labeling dependent on the cytidine deaminase AID, we show that after immunization with a particulate antigen, B cell memory appeared in several subsets, comprising clusters of immunoglobulin M-positive (IgM(+)) and IgG1(+) B cells in germinal center-like structures that persisted up to 8 months after immunization, as well as IgM(+) and IgG1(+) B cells with a memory phenotype outside of B cell follicles. After challenge, the IgG subset differentiated into plasmocytes, whereas the IgM subset reinitiated a germinal center reaction. This model, in which B cell memory appears in several layers with different functions, reconciles previous conflicting propositions.
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Germinal centre responses induced by more robust adjuvants such as sheep red blood cells, complete Freund's adjuvant or saponin-based adjuvants tend to peak at 2-4 weeks after vaccination and can persist at low frequencies for several months.
“Germinal centre responses induced by immunization with more robust adjuvants such as sheep red blood cells, complete Freund’s adjuvant or saponin-based adjuvants tend to peak slightly later, at 2–4 weeks after vaccination, and can persist at low frequencies for several months27–33.”
From SARS-CoV-2 mRNA vaccines induce persistent human germinal centre responses (2021) · cites this paper as [28]
Antigen-specific germinal centre B cells have been found to persist for at least one year, albeit at very low levels.
“antigen-specific germinal centre B cells have been found to persist for at least one year, albeit at very low levels28,30.”
From SARS-CoV-2 mRNA vaccines induce persistent human germinal centre responses (2021) · cites this paper as [28]
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- Authors
- Dogan, I., Bertocci, B., Vilmont, V., Delbos, F., Mégret, J., Storck, S., Reynaud, C.-A., & Weill, J.-C.
- Affiliations
- Hôpital Necker-Enfants Malades (FR)
- Corresponding author
- Reynaud, Claude-Agnès
- Weill, Jean-Claude
- Venue
- Nature Immunology
- Published
- 2009-10-25
- Volume
- 10
- Issue
- 12
- Pages
- 1292-1299
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- OpenAlex
- W2053095572
- Cited by
- 635
- References
- 45
- Citations by year
- 2026: 22 · 2025: 22 · 2024: 37 · 2023: 32 · 2022: 27 · 2021: 45 · 2020: 53 · 2019: 44 · 2018: 48 · 2017: 49 · 2016: 37 · 2015: 51 · 2014: 35 · 2013: 35 · 2012: 40
- FWCI
- 14.07
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- memory B cells, IgM memory B cells, germinal center, cytidine deaminase, secondary immune response, B cell follicles
- MeSH terms
- Animals, B-Lymphocytes, Cell Differentiation, Cytidine Deaminase, Immunoglobulin G, Immunoglobulin M, Immunologic Memory, Mutation, Phenotype, Germinal Center, Models, Animal, Mice
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