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首页> 外文期刊>Virology >In vitro induction of HIV-1 replication in resting CD4(+) T cells derived from individuals with undetectable plasma viremia upon stimulation with human T-cell leukemia virus type I
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In vitro induction of HIV-1 replication in resting CD4(+) T cells derived from individuals with undetectable plasma viremia upon stimulation with human T-cell leukemia virus type I

机译:在人类I细胞白血病病毒I型刺激下,血浆CD4(+)T细胞中静息的CD4(+)T细胞衍生的HIV-1复制的体外诱导

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摘要

Microbial coinfections have been associated with transient bursts of human immunodeficiency virus (HIV) viremia in patients. In this study we investigated whether human T-cell leukemia virus type I (HTLV-I), another human retrovirus that is prevalent among certain HIV-infected populations, can induce HIV-1 replication in patients who had been successfully treated with highly active antiretroviral therapy. We demonstrate that supernatants from HTLV-l-producing MT-2 cells can induce in vitro replication of HIV-I from highly purified, resting CD4(+) T cells obtained from individuals with undetectable plasma viremia. Depletion of proinflammatory cytokines from the supernatants reduced, but did not abrogate, the ability to induce HIV-1 replication, indicating that other factors such as HTLV-I Tax or Env also have a role. The HTLV-l-mediated effect does not require productive infection: exposure to heat-inactivated HTLV-I virions, purified Tax protein, or HTLV-I Env glycoprotein also induced expression of HIV-I. Furthermore, we demonstrate that coculture of resting CD4(+) T cells with autologous CD8(+) T cells markedly inhibits the HTLV-l-induced virus replication. Our results suggest that coinfection with HTLV-I may induce viral replication in the latent viral reservoirs; however, CD8(+) T cells may play an important role in controlling the spread of virus upon microbial stimulation. (C) 2000 Academic Press. [References: 33]
机译:微生物共感染与患者中人类免疫缺陷病毒(HIV)病毒血症的短暂爆发有关。在这项研究中,我们调查了I型人T细胞白血病病毒(HTLV-I)(在某些HIV感染人群中普遍存在的另一种人逆转录病毒)是否可以在已成功用高活性抗逆转录病毒治疗的患者中诱导HIV-1复制治疗。我们证明,从产生HTLV-1的MT-2细胞的上清液可以诱导HIV-1从高度纯化的静息CD4(+)T细胞的体外复制,该CD4(+)T细胞得自血浆病毒血症无法检测的个体。上清液中促炎细胞因子的消耗减少,但没有消除诱导HIV-1复制的能力,这表明其他因素(例如HTLV-1 Tax或Env)也起作用。 HTLV-1介导的作用不需要生产性感染:暴露于热灭活的HTLV-1病毒体,纯化的Tax蛋白或HTLV-1 Env糖蛋白也可诱导HIV-1的表达。此外,我们证明静息CD4(+)T细胞与自体CD8(+)T细胞的共培养显着抑制了HTLV-1诱导的病毒复制。我们的结果表明,HTLV-1的共感染可能会在潜在的病毒库中诱导病毒复制。但是,CD8(+)T细胞可能在微生物刺激后控制病毒的传播中起重要作用。 (C)2000年学术出版社。 [参考:33]

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