Open AccessREGULATION OF ANTIBODY RESPONSE BY AN IgG-ANTI-Ig AUTOANTIBODY OCCURRING DURING ALLOIMMUNIZATION
Author(s) -
Peter Terness,
Gerhard Opelz
Publication year - 1992
Publication title -
transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.45
H-Index - 204
eISSN - 1534-6080
pISSN - 0041-1337
DOI - 10.1097/00007890-199207000-00016
Subject(s) - autoantibody , antibody , antigen , immunology , spleen , b cell , immunoglobulin g , microbiology and biotechnology , chemistry , immunoglobulin fc fragments , immunoglobulin e , biology
We have shown previously that alloimmunized rats develop a broadly reactive IgG-antiimmunoglobulin autoantibody in addition to antidonor antibodies. The findings presented herein demonstrate that this "physiological" antibody suppresses antigen receptor-induced IgM production of B cells derived from rats of the same strain. When affinity-purified IgG-anti-Ig was added to cell cultures, the antibody production of B cells was maximally inhibited at the minute concentration of 0.9 pg/10(6) cells. Higher or lower IgG-anti-Ig concentrations resulted in weaker suppression. The same result was obtained when spleen lymphocytes were used instead of purified B cells. Based on the molecular weight of IgG and Avogadro's number, our results indicate that a few molecules of IgG-anti-Ig are sufficient to inhibit the antibody production of a single B cell. Activity at this minuscule concentration demonstrates that IgG-anti-Ig antibodies are exquisitely active immunoregulatory molecules. In addition to the stimulatory effect of IgM-anti-Ig rheumatoid factors reported by others, our findings define the second component of an immunoregulatory mechanism: suppression of the B cell response by an IgG-anti-Ig autoantibody produced during alloimmunization.