| Literature DB >> 25941367 |
Jonathan Richard1, Maxime Veillette1, Nathalie Brassard2, Shilpa S Iyer3, Michel Roger1, Loïc Martin4, Marzena Pazgier5, Arne Schön6, Ernesto Freire6, Jean-Pierre Routy7, Amos B Smith8, Jongwoo Park8, David M Jones8, Joel R Courter8, Bruno N Melillo8, Daniel E Kaufmann9, Beatrice H Hahn10, Sallie R Permar11, Barton F Haynes11, Navid Madani12, Joseph G Sodroski12, Andrés Finzi13.
Abstract
HIV-1-infected cells presenting envelope glycoproteins (Env) in the CD4-bound conformation on their surface are preferentially targeted by antibody-dependent cell-mediated cytotoxicity (ADCC). HIV-1 has evolved a sophisticated mechanism to avoid exposure of ADCC-mediating Env epitopes by down-regulating CD4 and by limiting the overall amount of Env at the cell surface. Here we report that small-molecule CD4-mimetic compounds induce the CD4-bound conformation of Env, and thereby sensitize cells infected with primary HIV-1 isolates to ADCC mediated by antibodies present in sera, cervicovaginal lavages, and breast milk from HIV-1-infected individuals. Importantly, we identified one CD4 mimetic with the capacity to sensitize endogenously infected ex vivo-amplified primary CD4 T cells to ADCC killing mediated by autologous sera and effector cells. Thus, CD4 mimetics hold the promise of therapeutic utility in preventing and controlling HIV-1 infection.Entities:
Keywords: ADCC; CD4 mimetics; HIV-1; envelope glycoproteins; gp120
Mesh:
Substances:
Year: 2015 PMID: 25941367 PMCID: PMC4443331 DOI: 10.1073/pnas.1506755112
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205