Novel Dolutegravir and Lenacapavir Resistance Patterns in Human Immunodeficiency Virus Type 2 Infection: A Case Report.

IF 3.8 4区 医学 Q2 IMMUNOLOGY
Open Forum Infectious Diseases Pub Date : 2024-11-29 eCollection Date: 2025-01-01 DOI:10.1093/ofid/ofae705
Jeroen J A van Kampen, Els van Nood, Rizwan Mahmud, Zoë Krullaars, Tess Voskamp, Mike Voskamp, Tess Nijssen, Jolanda J C Voermans, Charlotte Charpentier, Quentin Le Hingrat, David A M C van de Vijver, Rob A Gruters, Thibault Mesplède
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引用次数: 0

Abstract

Background: The treatment management of human immunodeficiency virus (HIV)-2 infection presents greater challenges compared to HIV-1 infection, primarily because of inherent resistance against non-nucleoside reverse transcriptase inhibitors. Integrase strand transfer inhibitors, particularly dolutegravir, have improved treatment outcomes for people with HIV-2. Lenacapavir, a novel and potent antiretroviral capsid inhibitor, offers additional therapeutic options. However, limited knowledge exists regarding HIV-2 resistance against dolutegravir and lenacapavir.

Methods: We report the case of a treatment-experienced individual who did not achieve virological suppression with regimens containing dolutegravir and lenacapavir. Clinical monitoring, genotypic and phenotypic resistance assays, and in silico structural modeling were performed.

Results: Lenacapavir was added to a failing regimen of boosted darunavir, twice daily dolutegravir, and 2 nucleoside reverse transcriptase inhibitors. Initially, this addition led to a decline in the viral load and increase in CD4+ T-cell count, despite the identification of a previously unreported combination of integrase resistance mutations. However, virological suppression was not achieved and viral load, although reduced, resumed increasing. This rebound was associated with the development of an N73D capsid substitution in HIV-2, which conferred resistance against lenacapavir. Based on cell-based assays predicting hypersusceptibility to bictegravir, the regimen was adjusted to oral lenacapavir plus bictegravir/emtricitabine/tenofovir alafenamide, resulting in a resumption in viral load decline.

Conclusions: Although lenacapavir demonstrated therapeutic potential, our case underscores the critical need to combine it with other fully active antiretroviral agents to prevent the rapid emergence of resistance and achieve long-term virological control in treatment-experienced individuals with HIV-2.

人类免疫缺陷病毒2型感染中新的多替格拉韦和那卡帕韦耐药模式:一例报告。
背景:与HIV-1感染相比,人类免疫缺陷病毒(HIV)-2感染的治疗管理面临更大的挑战,主要是因为其对非核苷类逆转录酶抑制剂的固有耐药性。整合酶链转移抑制剂,特别是dolutegravir,改善了HIV-2患者的治疗效果。Lenacapavir是一种新型有效的抗逆转录病毒衣壳抑制剂,提供了额外的治疗选择。然而,关于HIV-2对dolutegravir和lenacapavir耐药的了解有限。方法:我们报告了一例治疗经验丰富的个体,使用含有多替格拉韦和来那卡帕韦的方案没有达到病毒学抑制。进行了临床监测、基因型和表型耐药分析以及硅结构建模。结果:Lenacapavir被添加到一个失败的方案中,该方案增加了darunavir,每天两次的dolutegravir和2核苷逆转录酶抑制剂。最初,这种添加导致病毒载量下降和CD4+ t细胞计数增加,尽管鉴定了以前未报道的整合酶耐药突变组合。然而,没有达到病毒学抑制,病毒载量虽然降低,但恢复增加。这种反弹与HIV-2中N73D衣壳替代的发展有关,这赋予了对lenacapavir的抗性。基于预测比替他韦超敏感的细胞试验,将治疗方案调整为口服来那卡韦加比替他韦/恩曲他滨/替诺福韦alafenamide,导致病毒载量恢复下降。结论:尽管lenacapavir显示出治疗潜力,但我们的病例强调,迫切需要将其与其他完全有效的抗逆转录病毒药物联合使用,以防止耐药性的迅速出现,并在治疗经验丰富的HIV-2患者中实现长期病毒学控制。
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
Open Forum Infectious Diseases
Open Forum Infectious Diseases Medicine-Neurology (clinical)
CiteScore
6.70
自引率
4.80%
发文量
630
审稿时长
9 weeks
期刊介绍: Open Forum Infectious Diseases provides a global forum for the publication of clinical, translational, and basic research findings in a fully open access, online journal environment. The journal reflects the broad diversity of the field of infectious diseases, and focuses on the intersection of biomedical science and clinical practice, with a particular emphasis on knowledge that holds the potential to improve patient care in populations around the world. Fully peer-reviewed, OFID supports the international community of infectious diseases experts by providing a venue for articles that further the understanding of all aspects of infectious diseases.
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