Progress Note 2024: Curing HIV; Not in My Lifetime or Just Around the Corner?

Q1 Medicine Pathogens and Immunity Pub Date : 2024-03-01 eCollection Date: 2023-01-01 DOI:10.20411/pai.v8i2.665
Justin Harper, Michael R Betts, Mathias Lichterfeld, Michaela Müller-Trutwin, David Margolis, Katharine J Bar, Jonathan Z Li, Joseph M McCune, Sharon R Lewin, Deanna Kulpa, Dázon Dixon Diallo, Michael M Lederman, Mirko Paiardini
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Abstract

Once a death sentence, HIV is now considered a manageable chronic disease due to the development of antiretroviral therapy (ART) regimens with minimal toxicity and a high barrier for genetic resistance. While highly effective in arresting AIDS progression and rendering the virus untransmissible in people living with HIV (PLWH) with undetectable viremia (U=U) [1, 2]), ART alone is incapable of eradicating the "reservoir" of resting, latently infected CD4+ T cells from which virus recrudesces upon treatment cessation. As of 2022 estimates, there are 39 million PLWH, of whom 86% are aware of their status and 76% are receiving ART [3]. As of 2017, ART-treated PLWH exhibit near normalized life expectancies without adjustment for socioeconomic differences [4]. Furthermore, there is a global deceleration in the rate of new infections [3] driven by expanded access to pre-exposure prophylaxis (PrEP), HIV testing in vulnerable populations, and by ART treatment [5]. Therefore, despite outstanding issues pertaining to cost and access in developing countries, there is strong enthusiasm that aggressive testing, treatment, and effective viral suppression may be able to halt the ongoing HIV epidemic (ie, UNAIDS' 95-95-95 targets) [6-8]; especially as evidenced by recent encouraging observations in Sydney [9]. Despite these promising efforts to limit further viral transmission, for PLWH, a "cure" remains elusive; whether it be to completely eradicate the viral reservoir (ie, cure) or to induce long-term viral remission in the absence of ART (ie, control; Figure 1). In a previous salon hosted by Pathogens and Immunity in 2016 [10], some researchers were optimistic that a cure was a feasible, scalable goal, albeit with no clear consensus on the best route. So, how are these cure strategies panning out? In this commentary, 8 years later, we will provide a brief overview on recent advances and failures towards identifying determinants of viral persistence and developing a scalable cure for HIV. Based on these observations, and as in the earlier salon, we have asked several prominent HIV cure researchers for their perspectives.

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2024 年进展说明:治愈艾滋病;有生之年无法实现,还是指日可待?
由于抗逆转录病毒疗法(ART)疗程的开发,HIV 曾一度被宣判死刑,但现在已被认为是一种可以控制的慢性疾病,其毒性极低,而且基因抗药性的屏障很高。虽然抗逆转录病毒疗法在阻止艾滋病发展和使病毒在检测不到病毒血症(U=U)的艾滋病病毒感染者(PLWH)中不再传播方面非常有效[1, 2]),但仅靠抗逆转录病毒疗法无法根除静止的、潜伏感染的 CD4+ T 细胞 "储库",因为一旦停止治疗,病毒就会从这些细胞中重新扩散。据 2022 年估计,目前有 3 900 万 PLWH,其中 86% 意识到自己的感染状况,76% 正在接受抗逆转录病毒疗法[3]。截至 2017 年,在不考虑社会经济差异的情况下,接受抗逆转录病毒疗法治疗的 PLWH 的预期寿命接近正常[4]。此外,在接触前预防(PrEP)、易感染人群的艾滋病毒检测以及抗逆转录病毒疗法(ART)治疗范围扩大的推动下,全球新感染率有所下降[3][5]。因此,尽管发展中国家在成本和获取途径方面还存在一些问题,但人们对积极的检测、治疗和有效的病毒抑制可能会阻止艾滋病毒的持续流行(即联合国艾滋病规划署的 95-95-95 目标)[6-8]抱有极大的热情;尤其是最近在悉尼观察到的令人鼓舞的情况[9]。尽管这些限制病毒进一步传播的努力很有希望,但对于 PLWH 来说,"治愈 "仍然遥不可及;无论是彻底消除病毒库(即治愈),还是在没有抗逆转录病毒疗法的情况下诱导长期病毒缓解(即控制;图 1)。在《病原体与免疫》杂志于 2016 年主办的沙龙上[10],一些研究人员乐观地认为,治愈是一个可行的、可扩展的目标,尽管在最佳途径上还没有明确的共识。那么,这些治愈策略的效果如何呢?在 8 年后的这篇评论中,我们将简要概述在确定病毒持续存在的决定因素和开发可推广的艾滋病治愈方法方面的最新进展和失败。基于这些观察,与之前的沙龙一样,我们请几位著名的艾滋病治愈研究人员谈谈他们的看法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pathogens and Immunity
Pathogens and Immunity Medicine-Infectious Diseases
CiteScore
10.60
自引率
0.00%
发文量
16
审稿时长
10 weeks
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