TY - JOUR
T1 - SLAM family receptors control pro-survival effectors in germinal center B cells to promote humoral immunity
AU - Zhong, Ming Chao
AU - Lu, Yan
AU - Qian, Jin
AU - Zhu, Yingzi
AU - Dong, Lingli
AU - Zahn, Astrid
AU - Di Noia, Javier M.
AU - Karo-Atar, Danielle
AU - King, Irah L.
AU - Veillette, André
N1 - Funding Information:
This work was supported by the Canadian Institutes of Health Research (grants MT-14429, MOP-82906, and FDN-143338 to A. Veillette, grant PJT-166028 to J.M. Di Noia, and grant FRN-153048 to I.L. King). It was also supported by the National Natural Science Foundation of China (grant 81771754 to L. Dong). Y. Zhu is supported by a scholarship from the China Scholarship Council. J.M. Di Noia is a Chercheur-boursier de mérite from the Fonds de Recherche Santé de Québec. A. Veillette holds the Canada Research Chair on Signaling in the Immune System.
Publisher Copyright:
© 2020 Zhong et al.
PY - 2021/3/1
Y1 - 2021/3/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85096816080&partnerID=8YFLogxK
U2 - 10.1084/JEM.20200756
DO - 10.1084/JEM.20200756
M3 - Article
C2 - 33237304
AN - SCOPUS:85096816080
SN - 0022-1007
VL - 218
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 3
M1 - e20200756
ER -