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Getting the 'Kill' into 'Shock and Kill': Strategies to Eliminate Latent HIV

机译:让“杀死”进入“休克和杀戮”:消除潜伏的艾滋病毒的策略

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摘要

Despite the success of antiretroviral therapy (ART), there is currently no HIV cure and treatment is life long. HIV persists during ART due to long-lived and proliferating latently infected CD4+ T cells. One strategy to eliminate latency is to activate virus production using latency reversing agents (LRAs) with the goal of triggering cell death through virus-induced cytolysis or immune-mediated clearance. However, multiple studies have demonstrated that activation of viral transcription alone is insufficient to induce cell death and some LRAs may counteract cell death by promoting cell survival. Here, we review new approaches to induce death of latently infected cells through apoptosis and inhibition of pathways critical for cell survival, which are often hijacked by HIV proteins. Given advances in the commercial development of compounds that induce apoptosis in cancer chemotherapy, these agents could move rapidly into clinical trials, either alone or in combination with LRAs, to eliminate latent HIV infection.
机译:尽管抗逆转录病毒治疗(艺术品)成功,目前没有艾滋病毒治愈和治疗是终身。由于长期寿命和增殖的潜伏期的CD4 + T细胞,艾滋病毒持续存在。消除潜伏期的一种策略是使用潜伏的逆转剂(LRA)激活病毒产生,其目的是通过病毒诱导的细胞分解或免疫介导的间隙触发细胞死亡。然而,多项研究表明,单独的病毒转录的激活不足以诱导细胞死亡,一些LRA可以通过促进细胞存活来抵消细胞死亡。在这里,我们通过凋亡和对细胞存活至关重要的途径抑制,促使潜伏感染的细胞死亡的新方法常常被HIV蛋白淹没。鉴于诱导癌症化疗中凋亡的化合物的商业发展的进展,这些药剂可以迅速转化为单独或与LRA结合的临床试验,以消除潜伏的艾滋病毒感染。

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  • 来源
    《Cell Host & Microbe》 |2018年第1期|共13页
  • 作者单位

    Univ Melbourne Peter Doherty Inst Infect &

    Immun Dept Microbiol &

    Immunol Melbourne Vic Australia;

    Univ Melbourne Peter Doherty Inst Immun &

    Infect Melbourne Vic Australia;

    Univ Melbourne Peter Doherty Inst Immun &

    Infect Melbourne Vic Australia;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 普通生物学;
  • 关键词

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