Antigen Modulation Confers Protection to Red Blood Cells from Antibody through Fcγ Receptor Ligation
Author(s) -
Sean R. Stowell,
Justine S. Liepkalns,
Jeanne E. Hendrickson,
Kathryn R. GirardPierce,
Nicole H. Smith,
Connie M. Arthur,
James C. Zimring
Publication year - 2013
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.1300885
Subject(s) - ligation , antibody , autoantibody , immunology , complement fixation test , receptor , antigen , complement receptor , microbiology and biotechnology , complement system , chemistry , biology , biochemistry , serology
Autoantibodies and alloantibodies can damage self-tissue or transplanted tissues through either fixation of complement or ligation of FcγRs. Several pathways have been described that imbue self-tissues with resistance to damage from complement fixation, as a protective measure against damage from these Abs. However, it has been unclear whether parallel pathways exist to provide protection from FcγR ligation by bound Abs. In this article, we describe a novel pathway by which cell surface Ag is specifically decreased as a result of Ab binding (Ag modulation) to the extent of conferring protection to recognized cells from Fcγ-dependent clearance. Moreover, the Ag modulation in this system requires FcγR ligation. Together, these findings provide unique evidence of self-protective pathways for FcγR-mediated Ab damage.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom