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Co‐receptor and accessory regulation of B‐cell antigen receptor signal transduction
Author(s) -
Buhl Anne Matte,
Cambier John C.
Publication year - 1997
Publication title -
immunological reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.839
H-Index - 223
eISSN - 1600-065X
pISSN - 0105-2896
DOI - 10.1111/j.1600-065x.1997.tb01033.x
Subject(s) - b cell receptor , receptor , biology , microbiology and biotechnology , signal transduction , immune receptor , antigen , cd19 , b cell , immune system , immunology , antibody , biochemistry
Summary: The development and function of the immune system is precisely regulated to assure the generation of protective immune responses while avoiding autoimmunity. This regulation is accomplished by the engagement of a multitude of cell‐surface receptors which transduce signals that activate or regulate cell differentiative and proliferative pathways. In some cases biologic responses reflect the integration of signals generated by co‐aggregation of multiple receptors by complex ligands. For example, B‐cell responses to antigen receptor aggregation can be modulated by co‐aggregation of receptors for immunoglobulin G (FcγRIIB1), complement components (CR2). and 4aL2,6‐sialoglycoproteins (CD22). Here we review our recent studies of molecular mechanisms underlying co‐receptor modulation of B‐cell antigen receptor signaling. Our results define interesting circuitry involving interactions among the B‐cell antigen receptor, CD 19 and FcγRIIB1. CD 19 may function as an important integrator of positive and negative signals that regulate B‐cell antigen receptor signal output.