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利纳卡帕韦:一种新型注射用 HIV-1 衣壳抑制剂。

Lenacapavir: A novel injectable HIV-1 capsid inhibitor.

机构信息

Upstate University Hospital, Syracuse, New York.

Upstate University Hospital, Syracuse, New York; Binghamton University School of Pharmacy and Pharmaceutical Sciences, Johnson City, New York.

出版信息

Int J Antimicrob Agents. 2024 Jan;63(1):107009. doi: 10.1016/j.ijantimicag.2023.107009. Epub 2023 Oct 14.

Abstract

Patients living with multidrug-resistant (MDR) HIV have limited antiretroviral regimen options that provide durable viral suppression. Lenacapavir is a novel first-in-class inhibitor of HIV-1 capsid function with efficacy at various stages of the viral life cycle, and it is indicated for the treatment of MDR HIV-1 infection in combination with optimized background antiretroviral therapy. The favourable pharmacokinetic profile supports an every sixth month dosing interval of subcutaneous lenacapavir after an initial oral loading dose, which may advocate for continued adherence to antiretroviral therapy (ART) through the reduction of daily pill burden. The role of lenacapavir in promoting virologic suppression has been studied in patients with MDR HIV-1 on failing ART at baseline. Lenacapavir was well tolerated in clinical trials with the most common adverse effects including mild to moderate injection site reactions, gastrointestinal symptoms, and headache. Substitutions on the capsid molecule may confer resistance to lenacapavir by changing the binding potential. Cross-resistance to other antiretrovirals has not been observed. The unique mechanism of action, pharmacokinetics, and safety and efficacy of lenacapavir support its use for the management of MDR HIV-1 infection. Current studies are ongoing to evaluate the potential use of subcutaneous lenacapavir for pre-exposure prophylaxis (PrEP). Future studies will confirm the long-term clinical safety, efficacy, and resistance data for lenacapavir.

摘要

患有耐多药 (MDR) HIV 的患者可供选择的抗逆转录病毒方案有限,这些方案能提供持久的病毒抑制。Lenacapavir 是一种新型的 HIV-1 衣壳功能抑制剂,在病毒生命周期的各个阶段都具有疗效,它与优化的背景抗逆转录病毒疗法联合用于治疗 MDR HIV-1 感染。有利的药代动力学特征支持在初始口服负荷剂量后,每隔 6 个月皮下给予 lenacapavir,这可能通过减少每日服药负担来促进对抗逆转录病毒治疗 (ART) 的持续依从性。Lenacapavir 在促进病毒学抑制方面的作用已在基线时正在接受失败的 ART 的 MDR HIV-1 患者中进行了研究。在临床试验中,lenacapavir 的耐受性良好,最常见的不良反应包括轻度至中度注射部位反应、胃肠道症状和头痛。衣壳分子上的取代可能会通过改变结合潜力而对 lenacapavir 产生耐药性。尚未观察到对其他抗逆转录病毒药物的交叉耐药性。Lenacapavir 的独特作用机制、药代动力学以及安全性和疗效支持其用于治疗 MDR HIV-1 感染。目前正在进行评估皮下 lenacapavir 用于暴露前预防 (PrEP) 的潜在用途的研究。未来的研究将证实 lenacapavir 的长期临床安全性、疗效和耐药数据。

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