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

被引:1
|
作者
Tebas, Pablo [1 ]
Lynn, Kenn [1 ]
Azzoni, Livio [2 ]
Cocchella, Giorgio [1 ]
Papasavvas, Emmanouil [2 ]
Fair, Matthew [2 ]
Karanam, Brijesh [2 ]
Sharma, Paridhima [2 ]
Reeves, Jacqueline D. [3 ]
Petropoulos, Christos J. [3 ]
Lalley-Chareczko, Linden [4 ]
Kostman, Jay R. [5 ]
Short, William [1 ]
Mounzer, Karam [4 ]
Montaner, Luis J. [1 ,2 ]
机构
[1] Univ Penn, Philadelphia, PA USA
[2] Wistar Inst Anat & Biol, 3601 Spruce St, Philadelphia, PA 19104 USA
[3] Labcorp Monogram Biosci, San Francisco, CA USA
[4] Jonathan Lax Immune Disorders Treatment Ctr, Philadelphia, PA USA
[5] John Bell Hlth Ctr, Philadelphia Field Initiating Grp HIV 1 Trials, Philadelphia, PA USA
关键词
10-1074; 3BNC117; ART suppression; HIV; neutralizing antibody; PhenoSense; ANTIBODIES; VIREMIA;
D O I
10.1097/QAD.0000000000003575
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 mu g/ml and 1.5 mu g/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.
引用
收藏
页码:1203 / 1207
页数:5
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