Department of Medicine.
Department of Microbiology and Center for Cellular Immunotherapies.
J Clin Invest. 2021 Apr 1;131(7). doi: 10.1172/JCI144486.
BackgroundWe conducted a phase I clinical trial that infused CCR5 gene-edited CD4+ T cells to determine how these T cells can better enable HIV cure strategies.MethodsThe aim of trial was to develop RNA-based approaches to deliver zinc finger nuclease (ZFN), evaluate the effect of CCR5 gene-edited CD4+ T cells on the HIV-specific T cell response, test the ability of infused CCR5 gene-edited T cells to delay viral rebound during analytical treatment interruption, and determine whether individuals heterozygous for CCR5 Δ32 preferentially benefit. We enrolled 14 individuals living with HIV whose viral load was well controlled by antiretroviral therapy (ART). We measured the time to viral rebound after ART withdrawal, the persistence of CCR5-edited CD4+ T cells, and whether infusion of 10 billion CCR5-edited CD4+ T cells augmented the HIV-specific immune response.ResultsInfusion of the CD4+ T cells was well tolerated, with no serious adverse events. We observed a modest delay in the time to viral rebound relative to historical controls; however, 3 of the 14 individuals, 2 of whom were heterozygous for CCR5 Δ32, showed post-viral rebound control of viremia, before ultimately losing control of viral replication. Interestingly, only these individuals had substantial restoration of HIV-specific CD8+ T cell responses. We observed immune escape for 1 of these reinvigorated responses at viral recrudescence, illustrating a direct link between viral control and enhanced CD8+ T cell responses.ConclusionThese findings demonstrate how CCR5 gene-edited CD4+ T cell infusion could aid HIV cure strategies by augmenting preexisting HIV-specific immune responses.REGISTRATIONClinicalTrials.gov NCT02388594.FundingNIH funding (R01AI104400, UM1AI126620, U19AI149680, T32AI007632) was provided by the National Institute of Allergy and Infectious Diseases (NIAID), the National Institute on Drug Abuse (NIDA), the National Institute of Mental Health (NIMH), and the National Institute of Neurological Disorders and Stroke (NINDS). Sangamo Therapeutics also provided funding for these studies.
我们开展了一项 I 期临床试验,输注 CCR5 基因编辑的 CD4+T 细胞,以确定这些 T 细胞如何更好地实现 HIV 治愈策略。
试验的目的是开发基于 RNA 的方法来递送锌指核酸酶(ZFN),评估 CCR5 基因编辑的 CD4+T 细胞对 HIV 特异性 T 细胞反应的影响,测试输注的 CCR5 基因编辑 T 细胞在分析性治疗中断期间延迟病毒反弹的能力,并确定 CCR5Δ32 杂合子个体是否优先受益。我们招募了 14 名 HIV 感染者,他们的病毒载量通过抗逆转录病毒治疗(ART)得到很好的控制。我们测量了 ART 停药后病毒反弹的时间、CCR5 编辑的 CD4+T 细胞的持续存在,以及输注 100 亿个 CCR5 编辑的 CD4+T 细胞是否增强了 HIV 特异性免疫反应。
CD4+T 细胞输注耐受良好,无严重不良事件。与历史对照相比,我们观察到病毒反弹时间略有延迟;然而,14 名个体中有 3 名,其中 2 名是 CCR5Δ32 的杂合子,在最终失去病毒复制控制之前,表现出病毒血症的反弹后控制。有趣的是,只有这些个体的 HIV 特异性 CD8+T 细胞反应得到了实质性的恢复。我们在病毒复发时观察到其中一个重新激活的反应出现免疫逃逸,这直接表明病毒控制与增强的 CD8+T 细胞反应之间存在关联。
这些发现表明,CCR5 基因编辑的 CD4+T 细胞输注可以通过增强预先存在的 HIV 特异性免疫反应来辅助 HIV 治愈策略。
ClinicalTrials.gov NCT02388594。
美国国立卫生研究院(NIH)资助(R01AI104400、UM1AI126620、U19AI149680、T32AI007632)由国家过敏和传染病研究所(NIAID)、国家药物滥用研究所(NIDA)、国家心理健康研究所(NIMH)和国家神经疾病和中风研究所(NINDS)提供。Sangamo Therapeutics 也为这些研究提供了资金。