A broadly neutralizing macaque monoclonal antibody against the HIV-1 V3-Glycan patch

Author:

Wang Zijun1,Barnes Christopher O2,Gautam Rajeev3,Cetrulo Lorenzi Julio C1,Mayer Christian T1,Oliveira Thiago Y1,Ramos Victor1ORCID,Cipolla Melissa1,Gordon Kristie M1,Gristick Harry B2,West Anthony P2,Nishimura Yoshiaki3,Raina Henna3,Seaman Michael S4,Gazumyan Anna1,Martin Malcolm3,Bjorkman Pamela J2ORCID,Nussenzweig Michel C15,Escolano Amelia1ORCID

Affiliation:

1. Laboratory of Molecular Immunology, The Rockefeller University, New York, United States

2. Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States

3. Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, United States

4. Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Boston, United States

5. Howard Hughes Medical Institute. The Rockefeller University, New York, United States

Abstract

A small fraction of HIV-1- infected humans develop broadly neutralizing antibodies (bNAbs) against HIV-1 that protect macaques from simian immunodeficiency HIV chimeric virus (SHIV). Similarly, a small number of macaques infected with SHIVs develop broadly neutralizing serologic activity, but less is known about the nature of simian antibodies. Here, we report on a monoclonal antibody, Ab1485, isolated from a macaque infected with SHIVAD8 that developed broadly neutralizing serologic activity targeting the V3-glycan region of HIV-1 Env. Ab1485 neutralizes 38.1% of HIV-1 isolates in a 42-pseudovirus panel with a geometric mean IC50 of 0.055 µg/mLl and SHIVAD8 with an IC50 of 0.028 µg/mLl. Ab1485 binds the V3-glycan epitope in a glycan-dependent manner. A 3.5 Å cryo-electron microscopy structure of Ab1485 in complex with a native-like SOSIP Env trimer showed conserved contacts with the N332gp120 glycan and gp120 GDIR peptide motif, but in a distinct Env-binding orientation relative to human V3/N332gp120 glycan-targeting bNAbs. Intravenous infusion of Ab1485 protected macaques from a high dose challenge with SHIVAD8. We conclude that macaques can develop bNAbs against the V3-glycan patch that resemble human V3-glycan bNAbs.

Funder

NIH Center for HIV/AIDS Vaccine Immunology and Immunogen Discovery

National Institute of Allergy and Infectious Diseases

Bill and Melinda Gates Foundation

National Institutes of Health

Howard Hughes Medical Institute

Burroughs Wellcome Fund

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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