Baseline susceptibility of primary HIV-2 to entry inhibitors

• Author(s): Borrego, Pedro ; Calado, Rita ; Marcelino, José M. ; Bártolo, Inês ; Rocha, Cheila ; Cavaco-Silva, Patrícia ; Doroana, Manuela ; Antunes, Francisco ; Maltez, Fernando ; Caixas, Umbelina ; Barroso, Helena ; Taveira, Nuno
• Date: 2012
• Persistent ID: http://hdl.handle.net/10362/173662
• Origin: Repositório Institucional da UNL
• Subject(s): Pharmacology; Pharmacology (medical); Infectious Diseases; SDG 3 - Good Health and Well-being
• Document Type: Journal article
• Language: English
• Contributor(s): Instituto de Higiene e Medicina Tropical (IHMT); Centro de Estudos de Doenças Crónicas (CEDOC); NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM); RUN

Description

Background: The baseline susceptibility of primary HIV-2 to maraviroc (MVC) and other entry inhibitors is currently unknown. Methods: The susceptibility of 19 HIV-2 isolates obtained from asymptomatic and AIDS patients and seven HIV-1 clinical isolates to the fusion inhibitors enfuvirtide (ENF) and T-1249, and to the coreceptor antagonists AMD3100, TAK-779 and MVC, was measured using a TZM-bl cell-based assay. The 50% inhibitory concentration (IC 50), 90% inhibitory concentration (IC 90) and dose-response curve slopes were determined for each drug. Results: ENF and T-1249 were significantly less active on HIV-2 than on HIV-1 (211- and 2-fold, respectively). AMD3100 and TAK-779 inhibited HIV-2 and HIV-1 CXCR4 tropic (X4) and CCR5 tropic (R5) variants with similar IC 50 and IC 90 values. MVC, however, inhibited the replication of R5 HIV-2 variants with significantly higher IC 90 values (42.7 versus 9.7 nM; P<0.0001) and lower slope values (0.7 versus 1.3; P<0.0001) than HIV-1. HIV-2 R5 variants derived from AIDS patients were significantly less sensitive to MVC than variants from asymptomatic patients, this being inversely correlated with the absolute number of CD4 + T-cells. Conclusions: T-1249 is a potent inhibitor of HIV-2 replication indicating that new fusion inhibitors might be useful to treat HIV-2 infection. Coreceptor antagonists TAK-779 and AMD3100 are also potent inhibitors of HIV-2 replication. The reduced sensitivity of R5 variants to MVC, especially in severely immunodeficient patients, indicates that the treatment of HIV-2-infected patients with MVC might require higher dosages than those used in HIV-1 patients, and should be adjusted to the disease stage.