Author Identifier

Lois Balmer: https://orcid.org/0000-0001-5618-0555

Document Type

Journal Article

Publication Title

Immunology and Cell Biology

Volume

102

Issue

10

First Page

935

Last Page

948

Publisher

Wiley

School

School of Medical and Health Sciences

RAS ID

72564

Funders

Canadian Institutes of Health Research (PPE-129119) / Natural Sciences and Engineering Research Council of Canada (2019-05047) / Natural Sciences and Engineering Research Council of Canada / La Fondation de l’Hopital Maisonneuve-Rosemont / Fonds de recherche du Quebec - Sante

Comments

Aubin, A. M., Vdovenko, D., Collin, R., Balmer, L., Coderre, L., Morahan, G., ... & Lesage, S. (2024). Variations in the germinal center response revealed by genetically diverse mouse strains. Immunology and Cell Biology, 102(10), 935-948. https://doi.org/10.1111/imcb.12823

Abstract

The humoral response is complex and involves multiple cellular populations and signaling pathways. Bacterial and viral infections, as well as immunization regimens, can trigger this type of response, promoting the formation of microanatomical cellular structures called germinal centers (GCs). GCs formed in secondary lymphoid organs support the differentiation of high-affinity plasma cells and memory B cells. There is growing evidence that the quality of the humoral response is influenced by genetic variants. Using 12 genetically divergent mouse strains, we assessed the impact of genetics on GC cellular traits. At steady state, in the spleen, lymph nodes and Peyer's patches, we quantified GC B cells, plasma cells and follicular helper T cells. These traits were also quantified in the spleen of mice following immunization with a foreign antigen, namely, sheep red blood cells, in addition to the number and size of GCs. We observed both strain- and organ-specific variations in cell type abundance, as well as for GC number and size. Moreover, we find that some of these traits are highly heritable. Importantly, the results of this study inform on the impact of genetic diversity in shaping the GC response and identify the traits that are the most impacted by genetic background.

DOI

10.1111/imcb.12823

Creative Commons License

Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.

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