Heavily treatment-experienced patients with HIV: are new mechanisms of action enough?

IF 1.4 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Journal of International Medical Research Pub Date : 2024-12-01 DOI:10.1177/03000605241301883
Marisa B Brizzi, Tracy L Cable, Dimple C Patel, Kelli Williams, Zoe Adjei, Carl J Fichtenbaum
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Abstract

Antiretroviral (ARV) drug resistance poses a threat to ending the HIV epidemic. As the rates of integrase resistance continue to increase globally, the availability of options for HIV treatment becomes limited. Heavily treatment-experienced (HTE) people with HIV (PWH) are limited to two or fewer available fully active ARV classes and are more likely to have an AIDS-defining event. Appropriate identification and management of HTE PWH is crucial to improving patient outcomes and reducing the future spread of drug-resistant HIV. As treatment options become more limited owing to drug resistance, the availability of more potent drugs with a marked increase in virologic suppression is needed in the current ART era. The purpose of this narrative review is to review the identification of HTE PWH, novel mechanisms of resistance, and management of HTE PWH in resource-rich and resource-limited settings using novel ARVs and combination ART.

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接受过大量治疗的艾滋病患者:新的作用机制是否足够?
抗逆转录病毒药物耐药性对终止艾滋病毒流行构成威胁。随着整合酶耐药性在全球范围内持续增加,艾滋病毒治疗方案的可得性变得有限。接受过大量治疗的艾滋病毒感染者(PWH)仅限于两种或更少的可获得的完全有效的抗逆转录病毒药物,并且更有可能发生艾滋病定义事件。适当识别和管理HTE和PWH对于改善患者预后和减少耐药艾滋病毒的未来传播至关重要。由于耐药性导致治疗选择越来越有限,在目前的抗逆转录病毒治疗时代,需要提供更有效的药物,并显著增强病毒学抑制。这篇叙述性综述的目的是回顾HTE PWH的识别,新的耐药机制,以及在资源丰富和资源有限的环境下使用新型抗逆转录病毒药物和联合抗逆转录病毒药物治疗HTE PWH。
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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