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

M. Anthony Moody(International Vaccine Institute), Hua-Xin Liao(International Vaccine Institute), S. Munir Alam(International Vaccine Institute), Richard M. Scearce(International Vaccine Institute), M. Kelly Plonk(International Vaccine Institute), Daniel M. Kozink(International Vaccine Institute), Mark S. Drinker(International Vaccine Institute), Ruijun Zhang(International Vaccine Institute), Shi-Mao Xia(International Vaccine Institute), Laura L. Sutherland(International Vaccine Institute), Georgia D. Tomaras(International Vaccine Institute), Ian Giles(University College London), John C. Kappes(University of Alabama at Birmingham), Christina Ochsenbauer‐Jambor(University of Alabama at Birmingham), Tara G. Edmonds(University of Alabama at Birmingham), Melina Soares(The University of Texas Southwestern Medical Center), Gustavo Barbero(The University of Texas Southwestern Medical Center), Donald N. Forthal(University of California, Irvine), Gary Landucci(University of California, Irvine), Connie Y. Chang(Avid Bioservices (United States)), Steven W. King(Avid Bioservices (United States)), Anita Kavlie, Thomas N. Denny(International Vaccine Institute), Kwan-Ki Hwang(International Vaccine Institute), Pojen P. Chen(University of California, Los Angeles), Philip E. Thorpe(The University of Texas Southwestern Medical Center), David C. Montefiori(Duke Medical Center), Barton F. Haynes(International Vaccine Institute)
The Journal of Experimental Medicine
April 5, 2010
Cited by 55Open Access
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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 approximately 10 microg/ml. Anti-phospholipid mAbs inhibited PBMC HIV-1 infection in vitro by mechanisms involving binding to monocytes and triggering the release of MIP-1alpha and MIP-1beta. The release of these beta-chemokines explains both the specificity for R5 HIV-1 and the activity of these mAbs in PBMC cultures containing both primary lymphocytes and monocytes.


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