Your browser doesn't support javascript.
loading
GSK3732394: a Multi-specific Inhibitor of HIV Entry.
Wensel, David; Sun, Yongnian; Davis, Jonathan; Li, Zhufang; Zhang, Sharon; McDonagh, Thomas; Langley, David; Mitchell, Tracy; Tabruyn, Sebastien; Nef, Patrick; Cockett, Mark; Krystal, Mark.
Afiliación
  • Wensel D; ViiV Healthcare, Branford, Connecticut, USA.
  • Sun Y; Bristol-Myers Squibb, Wallingford, Connecticut, USA.
  • Davis J; Bristol-Myers Squibb, Waltham, Massachusetts, USA.
  • Li Z; ViiV Healthcare, Branford, Connecticut, USA.
  • Zhang S; ViiV Healthcare, Branford, Connecticut, USA.
  • McDonagh T; Bristol-Myers Squibb, Waltham, Massachusetts, USA.
  • Langley D; Bristol-Myers Squibb, Wallingford, Connecticut, USA.
  • Mitchell T; Bristol-Myers Squibb, Waltham, Massachusetts, USA.
  • Tabruyn S; TransCure bioServices, Archamps, France.
  • Nef P; TransCure bioServices, Archamps, France.
  • Cockett M; ViiV Healthcare, Branford, Connecticut, USA.
  • Krystal M; ViiV Healthcare, Branford, Connecticut, USA Mark.R.Krystal@viivhealthcare.com.
J Virol ; 93(20)2019 10 15.
Article en En | MEDLINE | ID: mdl-31375580
ABSTRACT
Long-acting antiretrovirals could provide a useful alternative to daily oral therapy for HIV-1-infected individuals. Building on a bi-specific molecule with adnectins targeting CD4 and gp41, a potential long-acting biologic, GSK3732394, was developed with three independent and synergistic modes of HIV entry inhibition that potentially could be self-administered as a long-acting subcutaneous injection. Starting with the bi-specific inhibitor, an α-helical peptide inhibitor was optimized as a linked molecule to the anti-gp41 adnectin, with each separate inhibitor exhibiting at least single-digit nanomolar (or lower) potency and a broad spectrum. Combination of the two adnectins and peptide activities into a single molecule was shown to have synergistic advantages in potency, the resistance barrier, and the ability to inhibit HIV-1 infections at low levels of CD4 receptor occupancy, showing that GSK3732394 can work in trans on a CD4+ T cell. Addition of a human serum albumin molecule prolongs the half-life in a human CD4 transgenic mouse, suggesting that it may have potential as a long-acting agent. GSK3732394 was shown to be highly effective in a humanized mouse model of infection. GSK3732394 is currently in clinical trials.IMPORTANCE There continue to be significant unmet medical needs for patients with HIV-1 infection. One way to improve adherence and decrease the likelihood of drug-drug interactions in HIV-1-infected patients is through the development of long-acting biologic inhibitors. Building on a bi-specific inhibitor approach targeting CD4 and gp41, a tri-specific molecule was generated with three distinct antiviral activities. The linkage of these three biologic inhibitors creates synergy that offers a series of advantages to the molecule. The addition of human serum albumin to the tri-specific inhibitor could allow it to function as a long-acting self-administered treatment for patients with HIV infection. This molecule is currently in early clinical trials.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: VIH-1 / Inhibidores de Fusión de VIH Límite: Animals / Humans Idioma: En Revista: J Virol Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: VIH-1 / Inhibidores de Fusión de VIH Límite: Animals / Humans Idioma: En Revista: J Virol Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos