| Literature DB >> 24210120 |
Lindsay Wieczorek1, Bruce K Brown, Camila Delsarto Macedo, Maggie Wesberry-Schmierer, Viseth Ngauy, Andrew Rosa Borges, Nelson L Michael, Mary A Marovich, David C Montefiori, Victoria R Polonis.
Abstract
Cultured primary peripheral blood mononuclear cells (PBMC) represent a potentially physiologic in vitro model of HIV-1 infection, but assessment of antibody-mediated HIV-1 neutralization using PBMC has been hindered by donor variability and lack of a sustainable individual PBMC source. To advance this model for HIV vaccine evaluation, intra- and inter-assay variability were assessed using monoclonal and polyclonal antibodies and PBMC targets from multiple HIV-seronegative donors. Inter-assay variability was introduced by using different PBMC for virus propagation, and more substantially, for assay targets. Neutralization titers varied by as much as 4 logs when using different individual donor PBMC as targets; variability was antibody-specific, with the greatest variation observed using an individual polyclonal plasma. Pooling of multiple PBMC donors significantly reduced median inter-assay variation to the level of intra-assay variation, suggesting a pathway forward for establishing a uniform, sustainable and standardized approach to the assessment of antibody function using a PBMC model. Published by Elsevier Inc.Entities:
Keywords: HIV-1 neutralization; Infectious molecular clones; Monoclonal antibodies; PBMC targets; Peripheral blood mononuclear cells; Primary isolates; Standardization
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Year: 2013 PMID: 24210120 DOI: 10.1016/j.virol.2013.09.014
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616