Journal article

Publication year: 1987

Pages: 737-743

Journal: Scandinavian Journal of Immunology

Volume number: 26

Issue number: 6

ISSN: 0300-9475

eISSN: 1365-3083

DOI Link: https://doi.org/10.1111/j.1365-3083.1987.tb02311.x

Publisher: Wiley

Abstract: 
Major histocompatibility complex (MHC) antibodies induce immune phagocytosis inhibition (IPI) which lasts for at least 7 days. IPI-inducing antibodies do not inhibit the phagocytosis mediated by the beta-glucan receptor. This corresponds well to recent findings that these antibodies do not interfere with the phagocytosis of deactivated saccharomyces, mediated by the mannose-fucose receptor, or polyacrylic acid particles, also mediated by non-Fc receptors. Substances that interact with certain MHC antigens or with Fc receptors, certain toxins that inhibit surface molecule mobility, and ciclosporin do not cause IPI and do not suppress the induction of IPI by MHC antibodies. These substances are: opioid peptides, insulin, penicillin G, immune complexes, aggregated IgG, Fc fragments, ciclosporin, botulinum C2 toxin, sodium azide. Some lectins and EDTA are inhibitory in a non-selective fashion, since the Fc receptor independent phagocytosis is also abrogated.

Harvard Citation style: NEPPERT, J. (1987) PERSISTENCE AND SELECTIVITY OF THE IMMUNE PHAGOCYTOSIS INHIBITION BY MAJOR HISTOCOMPATIBILITY COMPLEX ANTIBODIES, Scandinavian Journal of Immunology, 26(6), pp. 737-743. https://doi.org/10.1111/j.1365-3083.1987.tb02311.x

APA Citation style: NEPPERT, J. (1987). PERSISTENCE AND SELECTIVITY OF THE IMMUNE PHAGOCYTOSIS INHIBITION BY MAJOR HISTOCOMPATIBILITY COMPLEX ANTIBODIES. Scandinavian Journal of Immunology. 26(6), 737-743. https://doi.org/10.1111/j.1365-3083.1987.tb02311.x