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T-cell dysfunction in HIV-1 infection: targeting the inhibitors

机译:HIV-1感染中的T细胞功能障碍:靶向抑制剂

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Since AIDS emerged almost three decades ago, there have been considerable advances in the field of antiretroviral chemotherapy for those chronically infected with HIV-1. However, this therapy is noncurative and as our understanding of HIV-1 immunopathogenesis increases, it is becoming apparent that further therapeutic interventions are required to reverse the devastating effects of HIV-1 infection worldwide. While viral clearance remains the principle goal of HIV-1 treatment, this article describes immunotherapeutic options that target the immunological effects of the virus, to reduce its presence in the body and counteract viral-induced T-cell dysfunction and inhibition. Such approaches may augment existing antiretroviral therapy to overturn virus-induced T-cell anergy in the infected host, improving levels of immune control that reduce viremia and decrease the rate of transmission.
机译:自从大约三十年前出现艾滋病以来,针对那些长期感染HIV-1的人在抗逆转录病毒化学疗法领域取得了长足的进步。但是,这种疗法是非治愈性的,并且随着我们对HIV-1免疫发病机制的了解增加,显然需要采取进一步的治疗干预措施来扭转全世界HIV-1感染的破坏性影响。尽管清除病毒仍然是HIV-1治疗的主要目标,但本文介绍了针对病毒免疫作用的免疫治疗选择,以减少病毒在体内的存在并抵消病毒引起的T细胞功能障碍和抑制作用。此类方法可能会增强现有的抗逆转录病毒疗法,以推翻受感染宿主中病毒诱导的T细胞无反应,从而提高免疫控制水平,从而降低病毒血症并降低传播速度。

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