CROI 2018: Advances in Antiretroviral Therapy.

Q1 Medicine
Topics in antiviral medicine Pub Date : 2018-05-01
Hong-Van Tieu, Barbara S Taylor, Joyce Jones, Timothy J Wilkin
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引用次数: 0

Abstract

The 2018 Conference on Retroviruses and Opportunistic Infections (CROI) showcased exciting data on new investigational agents including MK-8591 and tri-specific antibody targeting 3 highly conserved epitopes on HIV-1 in a single antibody. Clinical trials of initial antiretroviral therapy (ART) and switch studies involving bictegravir/emtricitabine/tenofovir alafenamide were presented. Intensification of initial ART with integrase strand transfer inhibitors did not increase the risk of immune reconstitution inflammatory syndrome. Pharmacokinetic issues were discussed, including the substantial drug-drug interactions between efavirenz-based ART and hormonal contraception delivered via a vaginal ring. Studies on pre-ART drug resistance and emergence of drug resistance after initial and second-line ART in different settings and populations were highlighted. Novel technologies to identify drug resistance included a free, cloud-based web service for HIV genotyping analysis and a promising technology for point-of-care drug resistance mutations testing. New strategies to improve the HIV care continuum included home-based testing with initiation of same-day ART and stratified care with specialized clinics to serve those disengaged in care, but the data on financial incentives were not encouraging. Several studies provided insights into the impact of early ART on decreasing the size of the HIV reservoir in HIV-infected infants. Pertinent conference findings relating to women's health issues included similar clinical outcomes between breastfeeding and formula feeding HIV-infected women, the problem of viral rebound and ART nonadherence in pregnancy and postpartum.

CROI 2018:抗逆转录病毒治疗的进展。
2018年逆转录病毒和机会性感染会议(CROI)展示了新的研究药物的令人兴奋的数据,包括MK-8591和三特异性抗体,靶向HIV-1上的3个高度保守的单抗体表位。介绍了初始抗逆转录病毒治疗(ART)的临床试验和涉及比替格拉韦/恩曲他滨/替诺福韦阿拉那胺的转换研究。整合酶链转移抑制剂增强初始抗逆转录病毒治疗不增加免疫重建炎症综合征的风险。讨论了药代动力学问题,包括以依非韦伦为基础的抗逆转录病毒治疗与通过阴道环提供的激素避孕之间的实质性药物-药物相互作用。重点研究了不同环境和人群中抗逆转录病毒治疗前的耐药性以及初始和二线抗逆转录病毒治疗后耐药性的出现情况。确定耐药性的新技术包括用于艾滋病毒基因分型分析的免费、基于云的网络服务和用于即时耐药突变检测的有前途的技术。改善艾滋病毒护理连续性的新战略包括以家庭为基础的检测,并开始当天进行抗逆转录病毒治疗,以及由专门诊所为那些脱离护理的人提供分层护理,但财政激励方面的数据并不令人鼓舞。几项研究为早期抗逆转录病毒治疗对减少艾滋病毒感染婴儿体内艾滋病毒库大小的影响提供了见解。与妇女健康问题相关的会议调查结果包括母乳喂养和配方喂养感染艾滋病毒的妇女之间相似的临床结果、病毒反弹问题以及怀孕和产后不坚持抗逆转录病毒治疗的问题。
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
Topics in antiviral medicine
Topics in antiviral medicine Medicine-Pharmacology (medical)
CiteScore
1.80
自引率
0.00%
发文量
10
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