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IgG-mediated suppression of antibody responses: Hiding or snatching epitopes?

Journal

SCANDINAVIAN JOURNAL OF IMMUNOLOGY
Volume 92, Issue 4, Pages -

Publisher

WILEY
DOI: 10.1111/sji.12921

Keywords

B cells; blood epitope masking; complement; experimental animals; Fc receptors; Fc-gamma receptor; Rhesus; suppression; trogocytosis

Categories

Funding

  1. Uppsala University
  2. Swedish Research Council
  3. China Scholarship Council (CSC)
  4. Ellen, Walter, and Lennart Hesselman's Foundation
  5. King Gustaf V:s 80 Years Foundation
  6. Ollie and Elof Ericsson's Foundation
  7. Agnes and Mac Rudberg's Foundation
  8. Hans von Kantzow's Foundation

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Antibodies forming a complex with antigen in vivo can dramatically change the antibody response to this antigen. In some situations, the response will be a 100-fold stronger than in animals immunized with antigen alone, and in other situations, the response will be completely suppressed. IgG is known to suppress the antibody response, for example to erythrocytes, and this is used clinically in Rhesus prophylaxis. The mechanism behind IgG-mediated immune suppression is still not understood. Here, we will review studies performed in experimental animal models and discuss the various hypotheses put forward to explain the profound suppressive effect of IgG. We conclude that an exclusive role for negative regulation of B cells through Fc gamma RIIB, increased clearance of erythrocytes from the circulation or complement-mediated lysis is unlikely. Epitope masking, where IgG hides the epitope from B cells, or trogocytosis, where IgG removes the epitope from the erythrocyte, is compatible with many observations. These two mechanisms are not mutually exclusive. Moreover, it cannot be ruled out that clearance, in combination with other mechanisms, plays a role.

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