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The Journal of Immunology, Vol 132, Issue 2 622-626, Copyright © 1984 by American Association of Immunologists


ARTICLES

Modulation of human B cell immunoglobulin secretion by the C3b component of complement

GC Tsokos, M Berger and JE Balow

The human C3b component of complement was found to inhibit the differentiation of human B lymphocytes into immunoglobulin-secreting cells in vitro. Pokeweed mitogen (PWM)-induced plaque-forming cell (PFC) responses were inhibited by C3-coated zymosan particles and by purified human C3b. C3b inhibited the PWM-driven responses in a dose- dependent fashion, and it was necessary for C3b to be present in the early phases of the cultures. C3b acted directly on B cells rather than on helper T cells because it inhibited the PFC responses of MNC depleted of T cells and subsequently stimulated with a T cell- independent Epstein Barr virus mitogen. Furthermore, C3b failed to stimulate the generation of suppressor lymphocytes and/or monocytes that might have been responsible for the inhibition of B cell responses. Our results indicate that C3b or its fragments exert negative modulatory effects on human B lymphocyte responses.


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M. Jozsi, J. Prechl, Z. Bajtay, and A. Erdei
Complement Receptor Type 1 (CD35) Mediates Inhibitory Signals in Human B Lymphocytes
J. Immunol., March 15, 2002; 168(6): 2782 - 2788.
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