Bártolo, InêsBorrego, PedroGomes, PerpetuaGonçalves, Maria FátimaCaixas, UmbelinaVaz-Pinto, InêsTaveira, Nuno2023-08-232023-08-232019Bártolo I, Borrego P, Gomes P, Gonçalves F, Caixas U, Pinto IV, et al. In vitro evaluation of novel reverse transcriptase inhibitors TAF (Tenofovir alafenamide) and OBP-601 (2,3-didehydro-3-deoxy-4-ethynylthymidine) against multi-drug resistant primary isolates of HIV-2. Antiviral Research [Internet]. 1 de janeiro de 2019;161:85–9. Disponível em: https://www.sciencedirect.com/science/article/pii/S0166354218305424http://hdl.handle.net/10451/58974New antiretroviral drugs are needed to treat HIV-2 infected patients failing therapy. Herein, we evaluate the activity of novel reverse transcriptase inhibitors tenofovir alafenamide (TAF) and OBP-601(2,3-didehydro-3-deoxy-4-ethynylthymidine) against primary isolates from HIV-2 infected patients experiencing virologic failure. TAF and OBP-601 were tested against twelve primary isolates obtained from nine drug-experienced patients failing therapy and three drug naïve patients using a single-round infectivity assay in TZM-bl cells. The RT-coding region of pol was sequenced and the GRADE algorithm was used to identify resistance profiles and mutations. TAF and OBP-601 inhibited the replication of almost all isolates at a median EC50 of 0.27 nM and 6.83 nM, respectively. Two isolates showed moderate-level resistance to OBP-601 or TAF and two other isolates showed high-level resistance to OBP-601 or to both drugs. With one exception, all resistant viruses had canonical nucleoside reverse transcriptase inhibitors (NRTIs)-associated resistance mutations (K65R, N69S, V111I, Y115F, Q151M and M184V). Our results show that TAF has potent activity against most multi-drug resistant HIV-2 isolates and should be considered for the treatment of HIV-2 infected patients failing therapy.engHIV-2Susceptibility to TAFTDF and OBP-601Resistance mutationsjournal article2023-02-03cv-prod-110844810.1016/j.antiviral.2018.10.0182-s2.0-85057042987