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Experimental Approaches for Eliminating Latent HIV

机译:消除潜在艾滋病毒的实验方法

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ABSTRACT: Antiretroviral therapy (ART) can reduce HIV viral loads to undetectable levels and prevent disease progression. However, HIV persists in rare cellular reservoirs within ART-treated patients and rapidly reemerges if ART is stopped. Latently infected CD4+ T cells represent a major reservoir of HIV that persists during ART. Therefore, a cure for HIV must include methods that either permanently inactivate or eliminate latent virus. Experimental methods under investigation for eliminating latently infected cells include transplantation/gene therapy approaches intended to deplete the infected cells and replace them with HIV-resistant ones, and DNA editing strategies that are capable of damaging or excising non-expressing HIV proviruses. Alternatively, "activation-elimination," also known as "shock and kill," approaches aim to induce expression of latent virus, allowing the virus to be eliminated by viral cytopathic effects, immune effector mechanisms, or additional cells/antibodies that specifically target and kill cells expressing HIV proteins. Here, we describe these experimental approaches for eliminating latent HIV along with other recent advances in HIV cure research.
机译:摘要:抗逆转录病毒疗法(ART)可以将HIV病毒载量降低到无法检测到的水平并防止疾病进展。然而,在经过艺术治疗的患者中,HIV持续存在于罕见的细胞库中,如果停止了艺术,则迅速重新出现。潜在感染的CD4+ T细胞代表了在艺术期间持续存在的主要HIV储藏。因此,艾滋病毒的治疗必须包括永久失活或消除潜在病毒的方法。正在研究的消除潜在感染细胞的实验方法包括旨在耗尽感染细胞并用耐HIV耐HIV的细胞的移植/基因治疗方法,以及能够损害或削减非表达HIV HIV PREFIRES的DNA编辑策略。另外,“激活灭气”,也称为“冲击和杀伤”,旨在诱导潜在病毒表达,从而使病毒通过病毒细胞病毒作用,免疫效应机制或其他特定靶向和靶向靶向和靶向的细胞/抗体来消除病毒杀死表达HIV蛋白的细胞。在这里,我们描述了消除潜在艾滋病毒的这些实验方法以及HIV治疗研究的其他最新进展。

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