Anti-phospholipid human monoclonal antibodies inhibit CCR5-tropic HIV-1 and induce β-chemokines

Author:

Moody M. Anthony11,Liao Hua-Xin11,Alam S. Munir111,Scearce Richard M.1,Plonk M. Kelly1,Kozink Daniel M.1,Drinker Mark S.1,Zhang Ruijun1,Xia Shi-Mao1,Sutherland Laura L.1,Tomaras Georgia D.122,Giles Ian P.3,Kappes John C.445,Ochsenbauer-Jambor Christina4,Edmonds Tara G.4,Soares Melina6,Barbero Gustavo6,Forthal Donald N.7,Landucci Gary7,Chang Connie8,King Steven W.8,Kavlie Anita9,Denny Thomas N.1,Hwang Kwan-Ki1,Chen Pojen P.10,Thorpe Philip E.6,Montefiori David C.2,Haynes Barton F.112

Affiliation:

1. Duke Human Vaccine Institute and Department of Pediatrics, Department of Medicine, Department of Pathology

2. Department of Surgery, and Department of Immunology, Duke University Medical Center, Durham, NC, 27710

3. Centre for Rheumatology Research, University College London Division of Medicine and Medical Molecular Biology Unit, Institute of Child Health, University College, WC1E 6BT London, England, UK

4. Department of Medicine and Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35233

5. Veterans Affairs Medical Center Research Service, Birmingham, AL 35233

6. Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX 75390

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

8. Peregrine Pharmaceuticals, Inc., Tustin, CA 92780

9. Affitech AS, 0373 Oslo, Norway

10. Department of Medicine, University of California, Los Angeles, Los Angeles, CA 90095

Abstract

Traditional antibody-mediated neutralization of HIV-1 infection is thought to result from the binding of antibodies to virions, thus preventing virus entry. However, antibodies that broadly neutralize HIV-1 are rare and are not induced by current vaccines. We report that four human anti-phospholipid monoclonal antibodies (mAbs) (PGN632, P1, IS4, and CL1) inhibit HIV-1 CCR5-tropic (R5) primary isolate infection of peripheral blood mononuclear cells (PBMCs) with 80% inhibitory concentrations of <0.02 to ∼10 µg/ml. Anti-phospholipid mAbs inhibited PBMC HIV-1 infection in vitro by mechanisms involving binding to monocytes and triggering the release of MIP-1α and MIP-1β. The release of these β-chemokines explains both the specificity for R5 HIV-1 and the activity of these mAbs in PBMC cultures containing both primary lymphocytes and monocytes.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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