Abstract

ABSTRACTRecombinant soluble HIV-1 envelope glycoprotein (Env) SOSIP trimers are a design platform for inducing broadly neutralizing antibodies (bNAbs) by vaccination. To date, these and alternative designs of native-like trimers, given singly or in pairs, have not induced bNAbs in test animals such as rabbits or macaques. Here, we have evaluated whether trivalent and tetravalent combinations of SOSIP trimers from clades A, B, and C, delivered simultaneously or sequentially, induce better neutralizing antibody responses in rabbits than when given alone. None of the tested formulations led to the induction of bNAbs. We found that BG505 clade A trimers dominated the autologous NAb responses induced by combinations, which probably relates to the presence of immunodominant glycan holes on the BG505 trimer. Furthermore, autologous NAb responses to all individual trimers were reduced when they were delivered in combinations compared with when delivered alone, suggesting that immunogen interference had occurred. Finally, in a sequential regimen, a heterologous clade C trimer cross-boosted NAb responses that were primed by earlier immunizations with clade A and B trimers. Taken together, these findings should allow us to improve the design of immunization regimens based on native-like HIV-1 Env trimers.IMPORTANCE A successful HIV-1 vaccine most probably requires a trimeric envelope glycoprotein (Env) component, as Env is the only viral protein on the surface of the virus and therefore the only target for neutralizing antibodies. Native-like Env trimers can induce strain-specific neutralizing antibodies but not yet broadly neutralizing antibodies. To try to broaden the antibody response, we immunized rabbits with soluble native-like Env trimers from three different clades using monovalent, multivalent, and sequential regimens. We found that the neutralizing antibody response against each immunogen was reduced when the immunogens were delivered in combination or sequentially compared to the monovalent regimen. In contrast, when the Env trimers from different clades were delivered sequentially, the neutralizing antibody response could be cross-boosted. Although the combination of native-like Env trimers from different clades did not induce broadly neutralizing antibodies, the results provide clues on how to use native-like trimers in vaccination experiments.

Highlights

  • Recombinant soluble HIV-1 envelope glycoprotein (Env) SOSIP trimers are a design platform for inducing broadly neutralizing antibodies by vaccination

  • Sequential and cocktail immunization strategies have previously been explored for HIV-1 Env immunogens using DNA vaccines, recombinant gp120, or uncleaved gp140 immunogens [15,16,17,18,19,20]

  • These studies showed that cocktail and sequential immunization regimens induced higher neutralizing antibodies (NAbs) responses against easy-to-neutralize viruses than monovalent vaccines, and our findings are consistent with this (Fig. 5A to C)

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Summary

Introduction

Recombinant soluble HIV-1 envelope glycoprotein (Env) SOSIP trimers are a design platform for inducing broadly neutralizing antibodies (bNAbs) by vaccination. To date, these and alternative designs of native-like trimers, given singly or in pairs, have not induced bNAbs in test animals such as rabbits or macaques. Soluble native-like envelope glycoprotein (Env) trimers that mimic the native HIV spike and that can induce neutralizing antibodies (NAbs) against relatively neutralizationresistant (tier 2) autologous viruses are a design platform for immunogens intended to induce bNAbs. Since the description of the prototype native-like trimer, BG505 SOSIP.664, many more SOSIP or derivative designs have been described [1,2,3,4,5]. The principal goal, to induce neutralization breadth, has not yet been achieved, but one strategy is to try to build on the narrow-specificity autologous responses [4]

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