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Antiretroviral Drugs Alter the Content of Extracellular Vesicles from HIV-1-Infected Cells

机译:抗逆转录病毒药物改变HIV-1感染细胞的细胞外囊泡含量

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To date, the most effective treatment of HIV-1 is a combination antiretroviral therapy (cART), which reduces viral replication and reverses pathology. We investigated the effect of cART (RT and protease inhibitors) on the content of extracellular vesicles (EVs) released from HIV-1-infected cells. We have previously shown that EVs contain non-coding HIV-1 RNA, which can elicit responses in recipient cells. In this manuscript, we show that TAR RNA levels demonstrate little change with the addition of cART treatment in cell lines, primary macrophages, and patient biofluids. We determined possible mechanisms involved in the selective packaging of HIV-1 RNA into EVs, specifically an increase in EV-associated hnRNP A2/B1. More recent experiments have shown that several other FDA-approved drugs have the ability to alter the content of exosomes released from HIV-1-infected cells. These findings on cART-altered EV content can also be applied to general viral inhibitors (interferons) which are used to treat other chronic infections. Additionally, we describe unique mechanisms of ESCRT pathway manipulation by antivirals, specifically the targeting of VPS4. Collectively, these data imply that, despite antiretroviral therapy, EVs containing viral products are continually released and may cause neurocognitive and immunological dysfunction.
机译:迄今为止,HIV-1的最有效治疗方法是联合抗逆转录病毒疗法(cART),可减少病毒复制并逆转病理。我们调查了cART(RT和蛋白酶抑制剂)对HIV-1感染细胞释放的细胞外囊泡(EVs)含量的影响。先前我们已经表明,EV包含非编码HIV-1 RNA,它可以在受体细胞中引起应答。在此手稿中,我们显示,在细胞系,原代巨噬细胞和患者生物流体中加入cAR​​T处理后,TAR RNA水平几乎没有变化。我们确定了将HIV-1 RNA选择性包装入电动汽车的可能机制,特别是与电动汽车相关的hnRNP A2 / B1的增加。最近的实验表明,其他几种FDA批准的药物也具有改变从HIV-1感染细胞释放的外泌体含量的能力。这些关于cART改变的EV含量的发现也可以应用于用于治疗其他慢性感染的一般病毒抑制剂(干扰素)。此外,我们描述了抗病毒药物ESCRT途径操纵的独特机制,特别是针对VPS4的靶向。总体而言,这些数据表明,尽管进行了抗逆转录病毒治疗,但含有病毒产物的电动车仍在不断释放,并可能引起神经认知和免疫功能障碍。

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