Ram Renee R, Duatschek Paul, Margot Nicolas, Abram Michael, Geleziunas Romas, Hesselgesser Joseph, Callebaut Christian
Department of Clinical Virology, Gilead Sciences, Inc., Foster City, CA, USA.
Antivir Ther. 2020;25(3):163-169. doi: 10.3851/IMP3359.
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.
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.
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.
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.
维萨特利莫德(VES;GS-9620)是一种Toll样受体7(TLR7)激动剂,可直接激活人浆细胞样树突状细胞(pDC)和B淋巴细胞,从而直接和间接产生细胞因子并激活免疫。作为HIV缓解策略的一部分,正在对感染HIV-1的人群进行VES评估。在此,我们使用来自HIV阳性供体的免疫细胞培养物,研究了VES触发HIV特异性CD8 T细胞间接激活的潜力。
分离出在稳定抗逆转录病毒治疗下病毒学得到抑制的HIV阳性供体(n = 31)的外周血单个核细胞(PBMC)培养物,并用VES或赋形剂处理24小时。细胞用表面和细胞内荧光偶联抗体以及HIV特异性五聚体染色,然后通过流式细胞术进行分析。
用VES处理PBMC后,所有31名供体的CD8 T细胞激活(CD69)均呈现浓度依赖性增加,最高可达88%。在这些供体中,31名供体中有20名由于VES导致HIV特异性CD8 T细胞激活呈浓度依赖性增加,最高可达20.8%。对一部分供体(n = 14)进行了细胞内染色,其中5名显示出VES诱导的功能性HIV特异性CD8 T细胞激活,这是通过CD107a和/或肿瘤坏死因子(TNF)-α上调来评估的。
本研究表明,VES治疗可诱导供体来源的PBMC中功能性HIV特异性CD8 T细胞的激活。这些数据支持将VES作为HIV缓解策略的一部分,用于激活功能性HIV特异性CD8 T细胞的潜在用途。