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Activation of HIV-specific CD8+ T-cells from HIV+ donors by vesatolimod.
Ram, Renee R; Duatschek, Paul; Margot, Nicolas; Abram, Michael; Geleziunas, Romas; Hesselgesser, Joseph; Callebaut, Christian.
Affiliation
  • Ram RR; Department of Clinical Virology, Gilead Sciences, Inc., Foster City, CA, USA.
  • Duatschek P; Department of Clinical Virology, Gilead Sciences, Inc., Foster City, CA, USA.
  • Margot N; Department of Clinical Virology, Gilead Sciences, Inc., Foster City, CA, USA.
  • Abram M; Department of Clinical Virology, Gilead Sciences, Inc., Foster City, CA, USA.
  • Geleziunas R; Department of Clinical Virology, Gilead Sciences, Inc., Foster City, CA, USA.
  • Hesselgesser J; Department of Clinical Virology, Gilead Sciences, Inc., Foster City, CA, USA.
  • Callebaut C; Department of Clinical Virology, Gilead Sciences, Inc., Foster City, CA, USA.
Antivir Ther ; 25(3): 163-169, 2020.
Article in En | MEDLINE | ID: mdl-32420906
BACKGROUND: Vesatolimod (VES; GS-9620) is a Toll-like receptor 7 (TLR7) agonist that directly activates human plasmacytoid dendritic cells (pDCs) and B lymphocytes resulting in direct and indirect production of cytokines and immune activation. VES is being evaluated in HIV-1-infected people as part of an HIV remission strategy. Here we investigated the potential of VES to trigger indirect activation of HIV-specific CD8+ T-cells using immune cell cultures derived from HIV+ donors. METHODS: Peripheral blood mononuclear cell (PBMC) cultures derived from HIV+ donors virologically suppressed on stable antiretroviral therapy (n=31) were isolated and treated with VES or vehicle for 24 h. Cells were stained with surface and intracellular fluorescent conjugated antibodies and HIV-specific pentamers, and analysed by flow cytometry. RESULTS: Treatment of PBMCs with VES resulted in all 31 donors demonstrating a concentration dependent increase in CD8+ T-cell activation (CD69+) of up to 88%. Of these donors, 20 of 31 donors displayed a concentration-dependent increase in HIV-specific CD8+ T-cell activation due to VES with a maximum of 20.8%. Intracellular staining was performed in a subset of donors (n=14), 5 of which displayed VES-induced activation of functional HIV-specific CD8+ T-cells as assessed by CD107a and/or tumour necrosis factor (TNF)-α upregulation. CONCLUSIONS: This study demonstrates that VES treatment can induce the activation of functional HIV-specific CD8+ T-cells in donor derived PBMCs. These data support the potential use of VES to activate functional HIV-specific CD8+ T-cells as part of an HIV remission strategy.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pteridines / HIV Infections / CD8-Positive T-Lymphocytes / Anti-HIV Agents Limits: Humans Language: En Journal: Antivir Ther Journal subject: TERAPIA POR MEDICAMENTOS / VIROLOGIA Year: 2020 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pteridines / HIV Infections / CD8-Positive T-Lymphocytes / Anti-HIV Agents Limits: Humans Language: En Journal: Antivir Ther Journal subject: TERAPIA POR MEDICAMENTOS / VIROLOGIA Year: 2020 Document type: Article Affiliation country: United States Country of publication: United kingdom