Abstract

Antibody responses are crucial for the control of virus infection. Understanding of the mechanism of antibody induction is important for the development of a vaccine eliciting effective anti-virus antibodies. Virus-specific B cell receptor (BCR)/antibody repertoires are different among individuals, but determinants for this difference remain largely unclear. We have recently reported that a germline BCR immunoglobulin (IgG) gene polymorphism (VH3.33_ET or VH3.33_VI) in rhesus macaques is the determinant for induction of potent B404-class anti-simian immunodeficiency virus (SIV) neutralizing antibodies in neutralization-sensitive SIVsmH635FC infection. In the present study, we examined whether neutralization-resistant SIVsmE543-3 infection can induce the anti-SIV neutralizing antibodies associated with the germline VH3.33 polymorphism. Anti-SIVsmE543-3 neutralizing antibodies were induced in all the macaques possessing the VH3.33_ET allele, but not in those without VH3.33_ET, in the chronic phase of SIVsmE543-3 infection. Next generation sequencing analysis of BCR VH genes found B404-class antibody sequences only in those with VH3.33_ET. These results indicate that anti-SIVsmE543-3 neutralizing antibody induction associated with the germline BCR IgG gene polymorphism can be triggered by infection with neutralization-resistant SIVsmE543-3. This animal model would be useful for the elucidation of the mechanism of potent antibody induction against neutralization-resistant viruses.

Highlights

  • Development of an effective vaccine is a key for global control of infectious diseases

  • We previously reported a potent monoclonal anti-simian immunodeficiency virus (SIV) B404, and related B404-class neutralizing antibodies (NAbs), induced in rhesus macaques infected with SIVsmH635FC, a NAb-sensitive SIV strain obtained by passage from NAbresistant SIVsmE543-3-infected macaques [12,13]

  • Next-generation sequencing (NGS) analysis of B cell receptor (BCR) VH genes detected B404-class antibody sequences only in those macaques with VH3.33_ET. These results indicate that NAb induction associated with the germline Ig VH3.33 polymorphism can occur in NAb-resistant SIVsmE543-3 infection

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Summary

Introduction

Development of an effective vaccine is a key for global control of infectious diseases. We previously reported a potent monoclonal anti-simian immunodeficiency virus (SIV) B404, and related B404-class neutralizing antibodies (NAbs), induced in rhesus macaques infected with SIVsmH635FC, a NAb-sensitive SIV strain obtained by passage from NAbresistant SIVsmE543-3-infected macaques [12,13]. Infection of macaques possessing the VH3.33_ET allele with NAb-sensitive SIVsmH635FC induced B404-class antibodies that neutralize NAb-sensitive SIV strains, and NAb-resistant SIVsmE543-3. We examined the effect of the germline Ig VH3.33 polymorphism on antibody induction in neutralization-resistant SIVsmE543-3 infection. Next-generation sequencing (NGS) analysis of BCR VH genes detected B404-class antibody sequences only in those macaques with VH3.33_ET These results indicate that NAb induction associated with the germline Ig VH3.33 polymorphism can occur in NAb-resistant SIVsmE543-3 infection

Animal Experiments
Analysis of Plasma Neutralizing Activity
NGS Analysis of BCR IgG VH cDNAs
Results
Neutralizing Antibody Responses in SIVsmE543-3-Infected Rhesus Macaques
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