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

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...

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Detalles Bibliográficos
Autores principales: Moody, M. Anthony, Liao, Hua-Xin, Alam, S. Munir, Scearce, Richard M., Plonk, M. Kelly, Kozink, Daniel M., Drinker, Mark S., Zhang, Ruijun, Xia, Shi-Mao, Sutherland, Laura L., Tomaras, Georgia D., Giles, Ian P., Kappes, John C., Ochsenbauer-Jambor, Christina, Edmonds, Tara G., Soares, Melina, Barbero, Gustavo, Forthal, Donald N., Landucci, Gary, Chang, Connie, King, Steven W., Kavlie, Anita, Denny, Thomas N., Hwang, Kwan-Ki, Chen, Pojen P., Thorpe, Philip E., Montefiori, David C., Haynes, Barton F.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856026/
https://www.ncbi.nlm.nih.gov/pubmed/20368576
http://dx.doi.org/10.1084/jem.20091281
Descripción
Sumario: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.