Broadly Neutralizing Monoclonal Antibodies 2F5 and 4E10 Directed against the Human Immunodeficiency Virus Type 1 gp41 Membrane-Proximal External Region Protect against Mucosal Challenge by Simian-Human Immunodeficiency Virus SHIV Ba-L

Author:

Hessell Ann J.1,Rakasz Eva G.2,Tehrani David M.1,Huber Michael1,Weisgrau Kimberly L.2,Landucci Gary3,Forthal Donald N.3,Koff Wayne C.4,Poignard Pascal14,Watkins David I.2,Burton Dennis R.15

Affiliation:

1. Department of Immunology and Microbial Science and the International AIDS Vaccine Initiative Neutralizing Antibody Center, The Scripps Research Institute, La Jolla, California 92037

2. Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, Wisconsin 53711

3. Division of Infectious Diseases, Department of Medicine, University of California, Irvine, School of Medicine, Irvine, California 92697

4. International AIDS Vaccine Initiative, New York, New York

5. Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology, and Harvard University, Boston, Massachusetts 02114

Abstract

ABSTRACT The membrane-proximal external region (MPER) of HIV-1, located at the C terminus of the gp41 ectodomain, is conserved and crucial for viral fusion. Three broadly neutralizing monoclonal antibodies (bnMAbs), 2F5, 4E10, and Z13e1, are directed against linear epitopes mapped to the MPER, making this conserved region an important potential vaccine target. However, no MPER antibodies have been definitively shown to provide protection against HIV challenge. Here, we show that both MAbs 2F5 and 4E10 can provide complete protection against mucosal simian-human immunodeficiency virus (SHIV) challenge in macaques. MAb 2F5 or 4E10 was administered intravenously at 50 mg/kg to groups of six male Indian rhesus macaques 1 day prior to and again 1 day following intrarectal challenge with SHIV Ba-L . In both groups, five out of six animals showed complete protection and sterilizing immunity, while for one animal in each group a low level of viral replication following challenge could not be ruled out. The study confirms the protective potential of 2F5 and 4E10 and supports emphasis on HIV immunogen design based on the MPER region of gp41.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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