FCRL4 Is an Fc Receptor for Systemic IgA, but Not Mucosal Secretory IgA

被引:15
|
作者
Liu, Yanling [1 ]
Goroshko, Sofiya [1 ]
Leung, Leslie Y. T. [1 ]
Dong, Shilan [1 ]
Khan, Srijit [1 ]
Campisi, Paolo [2 ]
Propst, Evan J. [2 ]
Wolter, Nikolaus E. [2 ]
Grunebaum, Eyal [3 ]
Ehrhardt, Gotz R. A. [1 ]
机构
[1] Univ Toronto, Dept Immunol, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Hosp Sick Children, Dept Otolaryngol Head & Neck Surg, Toronto, ON M5G 1X8, Canada
[3] Hosp Sick Children, Div Immunol & Allergy, Toronto, ON M5G 1X8, Canada
来源
JOURNAL OF IMMUNOLOGY | 2020年 / 205卷 / 02期
关键词
IMMUNOGLOBULIN (IG)A1; B-CELLS; EXPRESSION; TISSUE; IDENTIFICATION;
D O I
10.4049/jimmunol.2000293
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Fc receptor-like (FCRL) 4 is an immunoregulatory receptor expressed on a subpopulation of human memory B cells of mucosa-associated lymphoid tissue. Fc receptor function of FCRL4 was demonstrated by binding of IgA to FCRL4 following heat aggregation of the Ig. In this study, we demonstrate that FCRL4 recognizes J chain-linked systemic IgA in the absence of heat aggregation. We further demonstrate that mucosal secretory IgA is not recognized by FCRL4 and that systemic IgA binding can be competitively inhibited by recombinant secretory component protein. Finally, we provide evidence that primary FCRL4-bearing human memory B cells are constitutively bound to IgA. Our study provides a mechanism for the negative regulatory activity of FCRL4 on AgR-mediated B cell activation.
引用
收藏
页码:533 / 538
页数:6
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