Oligonucleotide-lipid conjugates forming G-quadruplex structures are potent and pangenotypic hepatitis C virus entry inhibitors in vitro and ex vivo

Koutsoudakis, George; Paris de León, Alexia; Herrera, Carolina; Dorner, Marcus; Pérez Vilaró, Gemma, 1985-; Lyonnais, Sébastien; Grijalvo, Santiago; Eritja, Ramon; Meyerhans, Andreas; Mirambeau, Gilles; Díez Antón, Juana, 1962-

doi:http://dx.doi.org/10.1128/AAC.02354-16

Oligonucleotide-lipid conjugates forming G-quadruplex structures are potent and pangenotypic hepatitis C virus entry inhibitors in vitro and ex vivo

Citation

Koutsoudakis G, Paris de León A, Herrera C, Dorner M, Pérez Vilaró G, Lyonnais S et. Oligonucleotide-lipid conjugates forming G-quadruplex structures are potent and pangenotypic hepatitis C virus entry inhibitors in vitro and ex vivo. Antimicrobial Agents and Chemotherapy. 2017;61(5):e02354. DOI: 10.1128/AAC.02354-16

Abstract

A hepatitis C virus (HCV) epidemic affecting HIV-infected men who have sex with men (MSM) is expanding worldwide. In spite of the improved cure rates obtained with the new direct-acting antiviral drug (DAA) combinations, the high rate of reinfection within this population calls urgently for novel preventive interventions. In this study, we determined in cell culture and ex vivo experiments with human colorectal tissue that lipoquads, G-quadruplex DNA structures fused to cholesterol, are efficient HCV pangenotypic entry and cell-to-cell transmission inhibitors. Thus, lipoquads may be promising candidates for the development of rectally applied gels to prevent HCV transmission.