Suppr超能文献

整合酶链转移抑制剂时代泛耐药HIV-1的出现:一例报告

Pan-resistant HIV-1 emergence in the era of integrase strand-transfer inhibitors: a case report.

作者信息

Puertas Maria C, Ploumidis George, Ploumidis Michalis, Fumero Emilio, Clotet Bonaventura, Walworth Charles M, Petropoulos Christos J, Martinez-Picado Javier

机构信息

IrsiCaixa AIDS Research Institute, Germans Trias i Pujol University Hospital, Badalona, Spain.

Unit of Infectious Diseases, Hygeia Hospital, Athens, Greece.

出版信息

Lancet Microbe. 2020 Jul;1(3):e130-e135. doi: 10.1016/S2666-5247(20)30006-9. Epub 2020 Jun 11.

Abstract

BACKGROUND

In 2019, WHO reported that the prevalence of HIV-1 drug resistance to first-line regimens of non-nucleoside reverse transcriptase inhibitors is increasing in countries with a low number of therapeutic options. This increasing prevalence of drug resistance is an important threat to ending the AIDS pandemic, as it compromises individual clinical outcomes and increases the risk of transmission. In countries with a high number of therapeutic options, little global information is available regarding the prevalence of multidrug-resistant HIV-1 infections, which presents a potential challenge for the clinical management of people with HIV. Even after the approval of two new antiretroviral drug classes in 2007, which were intended to help alleviate this problem, some cases of infection with HIV-1 that show limited susceptibility to the five available antiretroviral classes have been described. We did a thorough in-vitro evaluation of the drug resistance profile of HIV-1 from an observational case to show that five-class pan-resistant clinical cases do exist.

METHODS

We investigated a case of a highly treatment-experienced Caucasian male with HIV-1 who had a poor virological response to previous combination antiretroviral therapy (ART) and who was not responding to a dolutegravir-based regimen. For the complete panel of approved antiretrovirals, we examined genotypic resistance using the Stanford HIV Drug Resistance Database interpretation algorithm, and we examined phenotypic resistance using the PhenoSense and Trofile assays. Using viral gp160 sequence analysis, we also explored the potential susceptibility of this virus to novel therapeutic drugs targeting viral envelope binding.

FINDINGS

The individual was diagnosed with HIV-1 on Sept 29, 1989. Since starting antiretroviral treatment in 1995, the individual had received more than 14 different antiretroviral drugs over the course of his illness. In November, 2017, a blood sample was collected from the individual and we did drug resistance analysis tests. We found that this individual was infected with a pan-resistant HIV-1 subtype B strain that showed broad genotypic and phenotypic cross-resistance to all approved antiretroviral drugs, including the newest second-generation integrase inhibitors, dolutegravir and bictegravir. With no remaining clinical options available, except for investigational drugs, this case provides evidence that new antiretroviral drugs with different mechanisms of action are needed.

INTERPRETATION

Our case report shows that HIV-1 multidrug cross-resistance remains an important concern, despite the extensive number of antiretroviral drugs currently available. Highly treatment-experienced patients, especially those who have been given suboptimal combination ART, can develop highly complex resistance-associated mutation patterns, conferring cross-resistance to all widely available ARTs. The identification and reporting of cases, such as the one described in this report, are needed to increase awareness of emerging trends that have the potential to affect patient management.

FUNDING

None.

摘要

背景

2019年,世界卫生组织报告称,在治疗选择有限的国家,HIV-1对一线非核苷类逆转录酶抑制剂治疗方案的耐药性患病率正在上升。耐药性患病率的上升是终结艾滋病流行的一个重要威胁,因为它会影响个体临床结局并增加传播风险。在治疗选择较多的国家,关于多重耐药HIV-1感染患病率的全球信息很少,这给HIV感染者的临床管理带来了潜在挑战。即使在2007年批准了两类新的抗逆转录病毒药物以帮助缓解这一问题之后,仍有一些对现有的五类抗逆转录病毒药物敏感性有限的HIV-1感染病例被报道。我们对1例观察病例的HIV-1耐药谱进行了全面的体外评估,以证明确实存在五类全耐药的临床病例。

方法

我们调查了1例有丰富治疗经验的白人男性HIV-1感染者,其对先前的联合抗逆转录病毒治疗(ART)病毒学反应不佳,且对基于多替拉韦的治疗方案无反应。对于所有已批准的抗逆转录病毒药物,我们使用斯坦福HIV耐药数据库解释算法检测基因型耐药性,并使用PhenoSense和Trofile检测法检测表型耐药性。通过病毒gp160序列分析,我们还探索了该病毒对靶向病毒包膜结合的新型治疗药物的潜在敏感性。

结果

该个体于1989年9月29日被诊断为感染HIV-1。自1995年开始抗逆转录病毒治疗以来,其在病程中接受了14种以上不同的抗逆转录病毒药物。2017年11月,采集了该个体的血样并进行耐药性分析检测。我们发现该个体感染了1株全耐药的HIV-1 B亚型毒株,该毒株对所有已批准的抗逆转录病毒药物,包括最新的第二代整合酶抑制剂多替拉韦和比克替拉韦,均表现出广泛的基因型和表型交叉耐药性。除了试验性药物外,已无其他临床治疗选择,该病例证明需要有不同作用机制的新型抗逆转录病毒药物。

解读

我们的病例报告表明,尽管目前有大量抗逆转录病毒药物,但HIV-1多重交叉耐药性仍然是一个重要问题。有丰富治疗经验的患者,尤其是那些接受了非最佳联合ART治疗的患者,可能会出现高度复杂的耐药相关突变模式,从而对所有广泛使用的ART药物产生交叉耐药性。需要识别和报告此类病例,如本报告中描述的病例,以提高对可能影响患者管理的新趋势的认识。

资金来源

无。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验