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FCRL4 Is an Fc Receptor for Systemic IgA, but Not Mucosal Secretory IgA
Author(s) -
Yanling Liu,
Sofiya Goroshko,
Leslie Y. T. Leung,
Shilan Dong,
Srijit Khan,
Paolo Campisi,
Evan J. Propst,
Nikolaus E. Wolter,
Eyal Grunebaum,
Götz R. A. Ehrhardt
Publication year - 2020
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.2000293
Subject(s) - secretory iga , recombinant dna , receptor , secretory component , immunoglobulin a , antibody , immunology , chemistry , biology , biochemistry , immunoglobulin g , gene
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.

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