Abstract
IgM exists as both a monomer on the surface of B cells and a pentamer secreted by plasma cells. Both pre-immune “natural” and antigen-induced “immune” IgM antibodies are important for protective immunity and for immune regulation of autoimmune processes by recognizing pathogens and self-antigens. Effector proteins interacting with the Fc portion of IgM, such as complement and complement receptors, have thus far been proposed but fail to fully account for the IgM-mediated protection and regulation. A major reason for this deficit in our understanding of IgM function seems to be lack of data on a long elusive Fc receptor for IgM (FcμR). We have recently identified a bona fide FcμR in both humans and mice. In this article we briefly review what we have learned so far about FcμR.
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Acknowledgments
The studies described in this article are accomplished based on the earlier studies on FcμR by Dr. Tatsuharu Ohno and Dr. Tetsuya Nakamura in the laboratory of Dr. Max Cooper and the authors wish to express our gratitude to them for their solid work and to Dr. Max Cooper for his great mentorship. This work was supported in part by National Institute of Health, National Institute of Allergy and Infectious Diseases Grants AI52243, R56AI82249, and R21AI94624 (to HK). Regretfully, Dr. Toshio Miyawaki, Professor Emeritus of Toyama University, was diseased on February 26, 2014, and we would like to offer our deepest sympathy.
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Kubagawa, H., Oka, S., Kubagawa, Y. et al. The Long Elusive IgM Fc Receptor, FcμR. J Clin Immunol 34 (Suppl 1), 35–45 (2014). https://doi.org/10.1007/s10875-014-0022-7
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DOI: https://doi.org/10.1007/s10875-014-0022-7