Recapitulation of HIV-1 Neutralization Breadth in Plasma by the Combination of Two Broadly Neutralizing Antibodies from Different Lineages in the Same SHIV-Infected Rhesus Macaque

Author:

Gai Yanxin1,Gao Nan1,Mou Zhaoyang1,Yang Chumeng1,Wang Libian1,Ji Wanshan1,Gu Tiejun1,Yu Bin1,Wang Chu1ORCID,Yu Xianghui12ORCID,Gao Feng134

Affiliation:

1. National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University, Changchun 130012, China

2. Key Laboratory for Molecular Enzymology and Engineering, The Ministry of Education, School of Life Sciences, Jilin University, Changchun 130012, China

3. Institute of Molecular and Medical Virology, School of Medicine, Jinan University, Guangzhou 510632, China

4. Key Laboratory of Viral Pathogenesis & Infection Prevention and Control, Jinan University, Ministry of Education, Guangzhou 510632, China

Abstract

Viral infection generally induces polyclonal neutralizing antibody responses. However, how many lineages of antibody responses can fully represent the neutralization activities in sera has not been well studied. Using the newly designed stable HIV-1 Env trimer as hook, we isolated two distinct broadly neutralizing antibodies (bnAbs) from Chinese rhesus macaques infected with SHIV1157ipd3N4 for 5 years. One lineage of neutralizing antibodies (JT15 and JT16) targeted the V2-apex in the Env trimers, similar to the J038 lineage bnAbs identified in our previous study. The other lineage neutralizing antibody (JT18) targeted the V3 crown region in the Env, which strongly competed with human 447-52D. Each lineage antibody neutralized a different set of viruses. Interestingly, when the two neutralizing antibodies from different lineages isolated from the same macaque were combined, the mixture had a neutralization breath very similar to that from the cognate sera. Our study demonstrated that a minimum of two different neutralizing antibodies can fully recapitulate the serum neutralization breadth. This observation can have important implications in AIDS vaccine design.

Funder

National Key Research and Development Program of China

the Research Fund for International Scientists of National Natural Science Fund of China

the National Natural Science Foundation of China

the Science and Technology Development Project of Jilin Province

the “Medicine + X” Interdisciplinary Innovation Team of Norman Bethune Health Science Center of Jilin University

Publisher

MDPI AG

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