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Fc‐Dependent IgG‐Mediated Suppression of the Antibody Response: Fact or Artefact?
Author(s) -
HEYMAN B.
Publication year - 1990
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1111/j.1365-3083.1990.tb02811.x
Subject(s) - epitope , antibody , monoclonal antibody , antigen , immunology , blocking antibody , effector , microbiology and biotechnology , biology , receptor , chemistry , biochemistry
IgG antibodies have been shown to suppress the antibody response to all epitopes of their specific antigen as well as those the IgG do not bind to, so‐called ‘non‐epitope‐specific suppression‘. The present study was undertaken to clarify whether there is a true IgG‐mediated Fc‐dependent suppression of Ihe antibody response. This question is of fundamental importance to the understanding of the mechanism behind this phenomenon. It is demonstrated that F(ab') 2 fragments of a monoclonal TNP (trinitrophenyl)‐specific IgG2a antibody are unable to suppress the murine in vitro non‐epitope‐specific plaque‐forming cell response against SRBC (sheep erythrocytes) when SRBC‐TNP is used as antigen. The same monoclonal IgG aniibody. when administered in intact form, is able lo induce up to 98% suppression of the SRBC‐specific antibody response. The lack of suppression is not due to mitogenic effects of pepsin in the F(ab') 2 fractions or increased breakdown of F(ab'); fragments, as compared with intact antibody, in the cultures. These data clearly demonstrate that there is indeed a highly efficient, Fc‐dependent, nonepitope‐specific suppressive mechanism mediated by IgG aniibodies and support a hypothesis involving binding of the anligcn‐anlibody complexes lo Fc receptors as a step in the effector mechanism.