首页> 美国卫生研究院文献>Current Controlled Trials in Cardiovascular Medicine >iHIVARNA phase IIa a randomized placebo-controlled double-blinded trial to evaluate the safety and immunogenicity of iHIVARNA-01 in chronically HIV-infected patients under stable combined antiretroviral therapy
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iHIVARNA phase IIa a randomized placebo-controlled double-blinded trial to evaluate the safety and immunogenicity of iHIVARNA-01 in chronically HIV-infected patients under stable combined antiretroviral therapy

机译:iHIVARNA IIa期一项随机安慰剂对照双盲试验用于评估iHIVARNA-01在稳定的抗逆转录病毒联合治疗下对慢性HIV感染患者的安全性和免疫原性

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摘要

BackgroundHIV therapeutic vaccination aims to improve the immune responses against HIV in order to control viral replication without the need for combined antiretroviral therapy (cART). iHIVARNA-01 is a novel vaccine combining mRNA delivery and T-cell immunogen (HTI) based on conserved targets of effective antiviral T-cell responses. In addition, it holds adequate stimuli required for activating antigen presenting cells (APC)s and co-activating specific T-cells (TriMix), including human CD40L, constitutively active TLR4 (caTLR4) and CD70. We propose that in-vivo targeting of dendritic cells (DCs) by direct administration of a HIV mRNA encoding these immune modulating proteins might be an attractive alternative to target DCs in vitro.
机译:背景技术HIV治疗性疫苗接种旨在改善针对HIV的免疫反应,以控制病毒复制,而无需联合使用抗逆转录病毒疗法(cART)。 iHIVARNA-01是一种新颖的疫苗,结合了基于有效抗病毒T细胞反应保守目标的mRNA递送和T细胞免疫原(HTI)。此外,它还具有激活抗原呈递细胞(APC)和共同激活特定T细胞(TriMix)所需的足够刺激,包括人CD40L,组成型活性TLR4(caTLR4)和CD70。我们提出通过直接给予编码这些免疫调节蛋白的HIV mRNA的树突状细胞(DC)的体内靶向可能是体外靶向DC的有吸引力的替代方法。

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