Cardiolipin Polyspecific Autoreactivity in Two Broadly Neutralizing HIV-1 Antibodies

Author:

Haynes Barton F.123,Fleming Judith123,St. Clair E. William123,Katinger Herman123,Stiegler Gabriela123,Kunert Renate123,Robinson James123,Scearce Richard M.123,Plonk Kelly123,Staats Herman F.123,Ortel Thomas L.123,Liao Hua-Xin123,Alam S. Munir123

Affiliation:

1. Duke University School of Medicine, Durham, NC 27710, USA.

2. Institute of Applied Microbiology, University of Agriculture, Vienna, Austria.

3. Tulane University School of Medicine, New Orleans, LA 70112, USA.

Abstract

The design of a human immunodeficiency virus–1 (HIV-1) immunogen that can induce broadly reactive neutralizing antibodies is a major goal of HIV-1 vaccine development. Although rare human monoclonal antibodies (mAbs) exist that broadly neutralize HIV-1, HIV-1 envelope immunogens do not induce these antibody specificities. Here we demonstrate that the two most broadly reactive HIV-1 envelope gp41 human mAbs, 2F5 and 4E10, are polyspecific autoantibodies reactive with the phospholipid cardiolipin. Thus, current HIV-1 vaccines may not induce these types of antibodies because of autoantigen mimicry of the conserved membrane-proximal epitopes of the virus. These results may have important implications for generating effective neutralizing antibody responses by using HIV-1 vaccines.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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