Potent and broad neutralization of HIV-1 by a llama antibody elicited by immunization

Author:

McCoy Laura E.11,Quigley Anna Forsman11,Strokappe Nika M.2,Bulmer-Thomas Bianca11,Seaman Michael S.3,Mortier Daniella4,Rutten Lucy2,Chander Nikita11,Edwards Carolyn J.11,Ketteler Robin1,Davis David4,Verrips Theo2,Weiss Robin A.11

Affiliation:

1. Wohl Virion Centre and Medical Research Council (MRC) Centre for Medical Molecular Virology, Division of Infection and Immunity; and MRC Laboratory for Molecular Cell Biology; University College London, London WC1E 6BT, England, UK

2. Biomolecular Imaging, Department of Biology, Institute of Biomembranes, Faculty of Science, Utrecht University, 3584 CH Utrecht, Netherlands

3. Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215

4. Department of Virology, Biomedical Primate Research Centre, 2280 GH Rijswijk, Netherlands

Abstract

Llamas (Lama glama) naturally produce heavy chain–only antibodies (Abs) in addition to conventional Abs. The variable regions (VHH) in these heavy chain–only Abs demonstrate comparable affinity and specificity for antigens to conventional immunoglobulins despite their much smaller size. To date, immunizations in humans and animal models have yielded only Abs with limited ability to neutralize HIV-1. In this study, a VHH phagemid library generated from a llama that was multiply immunized with recombinant trimeric HIV-1 envelope proteins (Envs) was screened directly for HIV-1 neutralization. One VHH, L8CJ3 (J3), neutralized 96 of 100 tested HIV-1 strains, encompassing subtypes A, B, C, D, BC, AE, AG, AC, ACD, CD, and G. J3 also potently neutralized chimeric simian-HIV strains with HIV subtypes B and C Env. The sequence of J3 is highly divergent from previous anti–HIV-1 VHH and its own germline sequence. J3 achieves broad and potent neutralization of HIV-1 via interaction with the CD4-binding site of HIV-1 Env. This study may represent a new benchmark for immunogens to be included in B cell–based vaccines and supports the development of VHH as anti–HIV-1 microbicides.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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