Abstract

Antigen-specific IgG antibodies, passively administered together with large particulate antigens such as erythrocytes, can completely suppress the antigen-specific antibody response. The mechanism behind has been elusive. Herein, we made the surprising observation that mice immunized with IgG anti-sheep red blood cells (SRBC) and SRBC, in spite of a severely suppressed anti-SRBC response, have a strong germinal center (GC) response. This occurred regardless of whether the passively administered IgG was of the same allotype as that of the recipient or not. Six days after immunization, the GC size and the number of GC B cells were higher in mice immunized with SRBC alone than in mice immunized with IgG and SRBC, but at the other time points these parameters were similar. GCs in the IgG-groups had a slight shift toward dark zone B cells 6 days after immunization and toward light zone B cells 10 days after immunization. The proportions of T follicular helper cells (TFH) and T follicular regulatory cells (TFR) were similar in the two groups. Interestingly, mice immunized with allogeneic IgG anti-SRBC together with SRBC mounted a vigorous antibody response against the passively administered suppressive IgG. Thus, although their anti-SRBC response was almost completely suppressed, an antibody response against allogeneic, and probably also syngeneic, IgG developed. This most likely explains the development of GCs in the absence of an anti-SRBC antibody response.

Highlights

  • Antibodies, passively administered together with their specific antigen, have the ability to modulate the specific antibody response

  • Specific IgG limits the amount of sheep red blood cells (SRBC) reaching the spleen [21, 24], and it seemed possible that IgG would limit the induction of splenic germinal center (GC)

  • BALB/c mice were immunized with SRBC ± IgGb anti-SRBC, and the GC response was followed for 4–14 days after immunization

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Summary

Introduction

Antibodies, passively administered together with their specific antigen, have the ability to modulate the specific antibody response This phenomenon is known as antibody feedback regulation [1,2,3]. IgG, passively administered together with erythrocytes, can completely suppress the erythrocyte-specific antibody response [13,14,15,16]. This has been used in the clinic since the 1960s to prevent immunization of RhD− mothers carrying RhD+ fetuses [17, 18]. RhD prophylaxis has dramatically decreased the incidence of hemolytic disease of the fetus and newborn [19]

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