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口服恩曲他滨和替诺福韦酯联合治疗预防含有 K65R 突变的耐替诺福韦的猴/人免疫缺陷病毒在猕猴中的疗效。

Prophylactic efficacy of oral emtricitabine and tenofovir disoproxil fumarate combination therapy against a tenofovir-resistant simian/human immunodeficiency virus containing the K65R mutation in macaques.

机构信息

Division of HIV/AIDS Prevention, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA.

出版信息

J Infect Dis. 2013 Aug 1;208(3):463-7. doi: 10.1093/infdis/jit189. Epub 2013 Apr 30.

DOI:10.1093/infdis/jit189
PMID:23633402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3699008/
Abstract

Daily preexposure prophylaxis (PrEP) with emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) is a novel strategy for preventing human immunodeficiency virus infection. We investigated in macaques whether FTC/TDF prevents transmission of a tenofovir-resistant simian/human immunodeficiency virus (SHIV) containing the K65R mutation. Six macaques received weekly a dose of FTC/TDF 3 days before rectal SHIV exposures and a second dose 2 hours after. Six untreated animals were controls. Animals were exposed rectally to escalating virus doses weekly for up to 28 weeks. PrEP significantly delayed infection with SHIVK65R (P = .028), although 4 of 6 FTC/TDF-treated macaques were infected at the end of the challenges. These findings highlight the need to closely monitor PrEP efficacy in areas with prevalent K65R.

摘要

每日暴露前预防(PrEP)用恩曲他滨/替诺福韦酯富马酸(FTC/TDF)是预防人类免疫缺陷病毒(HIV)感染的一种新策略。我们在猕猴中研究了 FTC/TDF 是否能预防含有 K65R 突变的耐替诺福韦的猴免疫缺陷病毒(SHIV)的传播。六只猕猴在直肠 SHIV 暴露前 3 天每周接受一次 FTC/TDF 剂量,暴露后 2 小时接受第二次剂量。六只未经治疗的动物作为对照。动物每周接受递增剂量的病毒直肠暴露,持续 28 周。PrEP 显著延迟了 SHIVK65R 的感染(P=0.028),尽管在挑战结束时,6 只 FTC/TDF 治疗的猕猴中有 4 只被感染。这些发现强调了在 K65R 流行的地区密切监测 PrEP 疗效的必要性。

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本文引用的文献

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Antiretroviral preexposure prophylaxis for heterosexual HIV transmission in Botswana.博茨瓦纳异性传播 HIV 中抗逆转录病毒的预先暴露预防。
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Penetration of tenofovir and emtricitabine in mucosal tissues: implications for prevention of HIV-1 transmission.替诺福韦和恩曲他滨在黏膜组织中的渗透:对预防 HIV-1 传播的意义。
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Protection against rectal transmission of an emtricitabine-resistant simian/human immunodeficiency virus SHIV162p3M184V mutant by intermittent prophylaxis with Truvada.特鲁瓦达间歇性预防可防止 emtricitabine 耐药的猴免疫缺陷病毒 SHIV162p3M184V 突变株经直肠传播。
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Generation and mucosal transmissibility of emtricitabine- and tenofovir-resistant SHIV162P3 mutants in macaques.在食蟹猴中生成并传播恩曲他滨和替诺福韦耐药性的 SHIV162P3 突变体。
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