SLAM family receptors control pro-survival effectors in germinal center B cells to promote humoral immunity

Author:

Zhong Ming-Chao1ORCID,Lu Yan1ORCID,Qian Jin1ORCID,Zhu Yingzi12ORCID,Dong Lingli2ORCID,Zahn Astrid3ORCID,Di Noia Javier M.3456ORCID,Karo-Atar Danielle7ORCID,King Irah L.78ORCID,Veillette André156ORCID

Affiliation:

1. Laboratory of Molecular Oncology, Institut de recherches cliniques de Montréal, Montréal, Québec, Canada

2. Department of Rheumatology and Immunology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

3. Laboratory of Mechanisms of Genetic Diversity, Institut de recherches cliniques de Montréal, Montréal, Québec, Canada

4. Department of Biochemistry and Molecular Medicine, University of Montréal, Montréal, Québec, Canada

5. Department of Medicine, University of Montréal, Montréal, Québec, Canada

6. Department of Medicine, McGill University, Montréal, Québec, Canada

7. Meakins-Christie Laboratories, Department of Medicine, McGill University Health Centre, Montréal, Québec, Canada

8. Department of Microbiology and Immunology, McGill University, Montréal, Québec, Canada

Abstract

Expression of the signaling lymphocytic activation molecule (SLAM)–associated protein (SAP) is critical for the germinal center (GC) reaction and T cell–dependent antibody production. However, when SAP is expressed normally, the role of the associated SLAM family receptors (SFRs) in these processes is nebulous. Herein, we established that in the presence of SAP, SFRs suppressed the expansion of the GC reaction but facilitated the generation of antigen-specific B cells and antibodies. SFRs favored the generation of antigen-reactive B cells and antibodies by boosting expression of pro-survival effectors, such as the B cell antigen receptor (BCR) and Bcl-2, in activated GC B cells. The effects of SFRs on the GC reaction and T cell–dependent antibody production necessitated expression of multiple SFRs, both in T cells and in B cells. Hence, while in the presence of SAP, SFRs inhibit the GC reaction, they are critical for the induction of T cell–mediated humoral immunity by enhancing expression of pro-survival effectors in GC B cells.

Funder

Canadian Institutes of Health Research

National Natural Science Foundation of China

China Scholarship Council

Fonds de Recherche Santé de Québec

Canada Research Chair

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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