Neutralization titer biomarker for antibody-mediated prevention of HIV-1 acquisition

Peter B. Gilbert(Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa), Yunda Huang(University of Washington), Allan C. deCamp(Fred Hutch Cancer Center), Shelly Karuna(Fred Hutch Cancer Center), Yuanyuan Zhang(Fred Hutch Cancer Center), Craig A. Magaret(Fred Hutch Cancer Center), Elena E. Giorgi(Los Alamos National Laboratory), Bette Korber(Los Alamos National Laboratory), Paul T. Edlefsen(Fred Hutch Cancer Center), Raabya Rossenkhan(Fred Hutch Cancer Center), Michal Juraska(Fred Hutch Cancer Center), Erika Rudnicki(Fred Hutch Cancer Center), Nidhi Kochar(Fred Hutch Cancer Center), Ying Huang(University of Washington), Lindsay N. Carpp(Fred Hutch Cancer Center), Dan H. Barouch(Beth Israel Deaconess Medical Center), Nonhlanhla N. Mkhize(National Health Laboratory Service), Tandile Hermanus(National Health Laboratory Service), Prudence Kgagudi(National Health Laboratory Service), Valerie Bekker(National Health Laboratory Service), Haajira Kaldine(National Health Laboratory Service), Rutendo E. Mapengo(National Health Laboratory Service), Amanda Eaton(Duke Medical Center), Elize Domin(Duke Medical Center), Carley West(Duke Medical Center), Wenhong Feng(Duke Medical Center), Haili Tang(Duke Medical Center), Kelly E. Seaton(Duke University), Jack Heptinstall(Duke University), Caroline Brackett(Duke University), Kelvin Chiong(Duke University), Georgia D. Tomaras(Duke University), P. Andrew(Family Health International 360), Bryan T. Mayer(Fred Hutch Cancer Center), Daniel B. Reeves(Fred Hutch Cancer Center), Magdalena E. Sobieszczyk(Columbia University Irving Medical Center), Nigel Garrett(Centre for the AIDS Programme of Research in South Africa), Jorge Sánchez(National University of San Marcos), Cynthia L. Gay(University of North Carolina at Chapel Hill), Joseph Makhema(Beth Israel Deaconess Medical Center), Carolyn Williamson(University of Cape Town), James I. Mullins(University of Washington), John Hural(Fred Hutch Cancer Center), Myron S. Cohen(University of North Carolina at Chapel Hill), Lawrence Corey(University of Washington), David C. Montefiori(Duke Medical Center), Lynn Morris(National Health Laboratory Service)
Nature Medicine
August 22, 2022
Cited by 122Open Access
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Abstract

Abstract The Antibody Mediated Prevention trials showed that the broadly neutralizing antibody (bnAb) VRC01 prevented acquisition of human immunodeficiency virus-1 (HIV-1) sensitive to VRC01. Using AMP trial data, here we show that the predicted serum neutralization 80% inhibitory dilution titer (PT 80 ) biomarker—which quantifies the neutralization potency of antibodies in an individual’s serum against an HIV-1 isolate—can be used to predict HIV-1 prevention efficacy. Similar to the results of nonhuman primate studies, an average PT 80 of 200 (meaning a bnAb concentration 200-fold higher than that required to reduce infection by 80% in vitro) against a population of probable exposing viruses was estimated to be required for 90% prevention efficacy against acquisition of these viruses. Based on this result, we suggest that the goal of sustained PT 80 >200 against 90% of circulating viruses can be achieved by promising bnAb regimens engineered for long half-lives. We propose the PT 80 biomarker as a surrogate endpoint for evaluation of bnAb regimens, and as a tool for benchmarking candidate bnAb-inducing vaccines.


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