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治愈HIV感染策略设计中的争议

Controversies in the Design of Strategies for the Cure of HIV Infection.

作者信息

de Gea-Grela Alejandro, Moreno Santiago

机构信息

Department of Internal Medicine, Hospital Universitario La Paz, 28034 Madrid, Spain.

Department of Infectious Diseases, Hospital Universitario Ramón y Cajal, Instituto Ramón y Cajal de Investigaciones Sanitarias (IRYCIS), Alcalá University, 28034 Madrid, Spain.

出版信息

Pathogens. 2023 Feb 15;12(2):322. doi: 10.3390/pathogens12020322.

Abstract

The cure for chronic human immunodeficiency virus (HIV) infections has been a goal pursued since the antiretroviral therapy that improved the clinical conditions of patients became available. However, the exclusive use of these drugs is not enough to achieve a cure, since the viral load rebounds when the treatment is discontinued, leading to disease progression. There are several theories and hypotheses about the biological foundations that prevent a cure. The main obstacle appears to be the existence of a latent viral reservoir that cannot be eliminated pharmacologically. This concept is the basis of the new strategies that seek a cure, known as kick and kill. However, there are other lines of study that recognize mechanisms of persistent viral replication in patients under effective treatment, and that would modify the current lines of research on the cure of HIV. Given the importance of these concepts, in this work, we propose to review the most recent evidence on these hypotheses, covering both the evidence that is positioned in favor and against, trying to expose what are some of the challenges that remain to be resolved in this field of research.

摘要

自从抗逆转录病毒疗法改善了患者的临床状况以来,治愈慢性人类免疫缺陷病毒(HIV)感染一直是人们追求的目标。然而,仅使用这些药物不足以实现治愈,因为停药后病毒载量会反弹,导致疾病进展。关于阻碍治愈的生物学基础有几种理论和假说。主要障碍似乎是存在一个无法通过药物消除的潜伏病毒库。这一概念是寻求治愈方法的新策略(即“激活并消灭”)的基础。然而,其他研究方向认识到在接受有效治疗的患者中存在持续病毒复制的机制,这将改变目前关于HIV治愈的研究方向。鉴于这些概念的重要性,在这项工作中,我们建议回顾关于这些假说的最新证据,涵盖支持和反对的证据,试图揭示该研究领域仍有待解决的一些挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/9961067/b71d0093d41a/pathogens-12-00322-g001.jpg

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