Susceptibility to 3BNC117 and 10-1074 in ART suppressed chronically infected persons

Author:

Tebas Pablo1,Lynn Kenn1,Azzoni Livio2,Cocchella Giorgio1,Papasavvas Emmanouil2,Fair Matthew2,Karanam Brijesh2,Sharma Paridhima2,Reeves Jacqueline D.3,Petropoulos Christos J.3,Lalley-Chareczko Linden4,Kostman Jay R.5,Short William1,Mounzer Karam4,Montaner Luis J.1

Affiliation:

1. University of Pennsylvania

2. The Wistar Institute, Philadelphia, PA

3. Labcorp-Monogram Biosciences, South San Francisco, CA

4. Jonathan Lax Immune Disorders Treatment Center

5. John Bell Health Center, Philadelphia Field Initiating Group for HIV-1 Trials, Philadelphia, PA, USA.

Abstract

Objective: The aim of this study was to assess the susceptibility of HIV to two HIV monoclonal antibodies (bnAbs), 3BNC117 and 10-1074, in individuals with chronically antiretroviral therapy (ART) suppressed HIV infection. Design: The susceptibility of bnAbs was determined using the PhenoSense mAb Assay, which is a cell-based infectivity assay designed to assess the susceptibility of luciferase-reporter pseudovirions. This assay is the only Clinical Laboratory Improvement Ammendment (CLIA)/College of American Pathologist (CAP) compliant screening test specifically developed for evaluating bnAb susceptibility in people with HIV infection. Method: The susceptibility of luciferase-reporter pseudovirions, derived from HIV-1 envelope proteins obtained from peripheral bloodmononuclear cells of 61 ART-suppressed individuals, to 3BNC117 and 10-1074 bnAbs was assessed using the PhenoSense mAb assay. Susceptibility was defined as an IC90 of <2.0 μg/ml and 1.5 μg/ml for 3BNC117 and 10-1074, respectively. Results: About half of the individuals who were chronically infected and virologically suppressed were found to harbor virus with reduced susceptibility to one or both of the tested bnAbs. Conclusions: The reduced combined susceptibility of 3BNC117 and 10-1074 highlights a potential limitation of using only two bnAbs for pre-exposure prophylaxis or treatment. Further studies are needed to define and validate the clinical correlates of bnAb susceptibility.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Immunology,Immunology and Allergy

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