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Closing the door to human immunodeficiency virus

机译:关上人类免疫缺陷病毒之门

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The pandemic of human immunodeficiency virus type one ( HIV-1 ), the major etiologic agent of acquired immunodeficiency disease ( AIDS ), has led to over 33 million people living with the virus, among which 18 million are women and children. Until now, there is neither an effective vaccine nor a therapeutic cure despite over 30 years of efforts. Although the Thai RV144 vaccine trial has demonstrated an efficacy of 31.2%, an effective vaccine will likely rely on a breakthrough discovery of immunogens to elicit broadly reactive neutralizing antibodies, which may take years to achieve. Therefore, there is an urgency of exploring other prophylactic strategies. Recently, antiretroviral treatment as prevention is an exciting area of progress in HIV-1 research. Although effective, the implementation of such strategy faces great financial, political and social challenges in heavily affected regions such as developing countries where drug resistant viruses have already been found with growing incidence. Activating latently infected cells for therapeutic cure is another area of challenge. Since it is greatly difficult to eradicate HIV-1 after the establishment of viral latency, it is necessary to investigate strategies that may close the door to HIV-1 . Here, we review studies on non-vaccine strategies in targeting viral entry, which may have critical implications for HIV-1 prevention.
机译:第一型人类免疫缺陷病毒(HIV-1)的大流行是获得性免疫缺陷疾病(AIDS)的主要病原体,已经导致超过3300万人感染该病毒,其中1800万是妇女和儿童。经过30多年的努力,到目前为止,还没有有效的疫苗或治疗方法。尽管Thai RV144疫苗试验显示出31.2%的功效,但有效的疫苗可能将依靠突破性的免疫原发现来引发具有广泛反应性的中和抗体,这可能需要数年才能实现。因此,迫切需要探索其他预防策略。最近,抗逆转录病毒治疗作为预防手段是HIV-1研究的一个令人兴奋的领域。尽管有效,但在受严重影响的地区(如发展中国家,已发现耐药病毒的发病率不断上升)中,实施这种战略面临巨大的财政,政治和社会挑战。激活潜伏感染的细胞进行治疗是另一个挑战。由于在建立病毒潜伏期后要根除HIV-1非常困难,因此有必要研究可能关闭HIV-1大门的策略。在这里,我们回顾针对靶向病毒进入的非疫苗策略的研究,这可能对HIV-1预防具有关键意义。

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