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The Second-Generation Maturation Inhibitor GSK3532795 Maintains Potent Activity Toward HIV Protease Inhibitor-Resistant Clinical Isolates.
Ray, Neelanjana; Li, Tianbo; Lin, Zeyu; Protack, Tricia; van Ham, Petronella Maria; Hwang, Carey; Krystal, Mark; Nijhuis, Monique; Lataillade, Max; Dicker, Ira.
Afiliación
  • Ray N; *Bristol-Myers Squibb, Research & Development, Princeton, NJ; †Bristol-Myers Squibb Virology, Wallingford, CT; ‡Currently, Tianbo Li, Genentech, South San Francisco, CA; Mark Krystal, Max Lataillade, and Ira Dicker, ViiV Healthcare, Wallingford, CT; §Department of Medical Microbiology, Virology, UMC Utrecht, Utrecht, the Netherlands; and ‖Currently, Carey Hwang, Global Clinical Development, Infectious Diseases, Merck, Kenilworth, NJ.
J Acquir Immune Defic Syndr ; 75(1): 52-60, 2017 05 01.
Article en En | MEDLINE | ID: mdl-28234686
ABSTRACT

BACKGROUND:

Protease inhibitor (PI)-resistant HIV-1 isolates with primary substitutions in protease (PR) and secondary substitutions in Gag could potentially exhibit cross-resistance to maturation inhibitors. We evaluated the second-generation maturation inhibitor, GSK3532795, for activity toward clinical isolates with genotypic and phenotypic characteristics associated with PI resistance (longitudinal).

METHODS:

Longitudinal clinical isolates from 15 PI-treated patients and 7 highly PI-resistant (nonlongitudinal) viruses containing major and minor PI resistance-associated mutations were evaluated for GSK3532795 sensitivity. Phenotypic sensitivity was determined using the PhenoSense Gag/PR assay (Monogram Biosciences) or in-house single- and multiple-cycle assays. Changes from baseline [CFB; ratio of post- to pre-treatment FC-IC50 (fold-change in IC50 versus wild-type virus)] <3 were considered to be within the no-effect level.

RESULTS:

All nonlongitudinal viruses tested were sensitive to GSK3532795 (FC-IC50 range 0.16-0.68). Among longitudinal isolates, all post-PI treatment samples had major PI resistance-associated mutations in PR and 17/21 had PI resistance-associated changes in Gag. Nineteen of the 21 post-PI treatment samples had GSK3532795 CFB <3. Median (range) CFB was 0.83 (0.05-27.4) [Monogram (11 patients)] and 1.5 (1.0-2.2) [single-cycle (4 patients)]. The 2 post-PI treatment samples showing GSK3532795 CFB >3 (Monogram) were retested using single- and multiple-cycle assays. Neither sample had meaningful sensitivity changes in the multiple-cycle assay. Gag changes were not associated with an increased GSK3532795 CFB.

CONCLUSIONS:

GSK3532795 maintained antiviral activity against PI-resistant isolates with emergent PR and/or Gag mutations. This finding supports continued development of GSK3532795 in treatment-experienced patients with or without previous PI therapy.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / VIH / Inhibidores de la Proteasa del VIH / Farmacorresistencia Viral Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / VIH / Inhibidores de la Proteasa del VIH / Farmacorresistencia Viral Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2017 Tipo del documento: Article