vesatolimod激活HIV阳性供者的HIV特异性CD8+ t细胞。

IF 2.3 4区 医学 Q4 INFECTIOUS DISEASES
Antiviral Therapy Pub Date : 2020-01-01 DOI:10.3851/IMP3359
Renee R Ram, Paul Duatschek, Nicolas Margot, Michael Abram, Romas Geleziunas, Joseph Hesselgesser, Christian Callebaut
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引用次数: 7

摘要

背景:Vesatolimod;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(pDCs)和B淋巴细胞,导致直接和间接产生细胞因子和免疫激活。作为艾滋病毒缓解战略的一部分,正在对HIV-1感染者进行VES评估。在这里,我们研究了VES触发HIV特异性CD8+ t细胞间接激活的潜力,使用来自HIV+供体的免疫细胞培养物。方法:分离经稳定抗逆转录病毒治疗病毒抑制的HIV+供体(n=31)外周血单个核细胞(PBMC)培养物,用VES或载体处理24小时。细胞表面和细胞内荧光结合抗体和HIV特异性五聚体染色,流式细胞术分析。结果:用VES治疗pbmc导致所有31名供者CD8+ t细胞激活(CD69+)的浓度依赖性增加高达88%。在这些供者中,31名供者中有20名由于VES而表现出hiv特异性CD8+ t细胞激活的浓度依赖性增加,最高为20.8%。对一部分供体(n=14)进行细胞内染色,其中5例通过CD107a和/或肿瘤坏死因子(TNF)-α上调来评估,显示出ves诱导的功能性hiv特异性CD8+ t细胞活化。结论:本研究表明,VES治疗可诱导供体源性pbmc中功能性hiv特异性CD8+ t细胞的活化。这些数据支持VES激活功能性HIV特异性CD8+ t细胞作为HIV缓解策略的一部分的潜在用途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Activation of HIV-specific CD8+ T-cells from HIV+ donors by vesatolimod.

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.

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来源期刊
Antiviral Therapy
Antiviral Therapy 医学-病毒学
CiteScore
2.60
自引率
8.30%
发文量
35
审稿时长
4-8 weeks
期刊介绍: Antiviral Therapy (an official publication of the International Society of Antiviral Research) is an international, peer-reviewed journal devoted to publishing articles on the clinical development and use of antiviral agents and vaccines, and the treatment of all viral diseases. Antiviral Therapy is one of the leading journals in virology and infectious diseases. The journal is comprehensive, and publishes articles concerning all clinical aspects of antiviral therapy. It features editorials, original research papers, specially commissioned review articles, letters and book reviews. The journal is aimed at physicians and specialists interested in clinical and basic research.
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