• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一线基于蛋白酶抑制剂的抗逆转录病毒治疗期间 HIV-1 RNA 抑制至<5 拷贝/ml 的时间 - 残余病毒血症对治疗成功有何影响?

Time to HIV-1 RNA suppression below 5 copies/ml during first-line protease inhibitor-based antiretroviral treatment - any impact of residual viremia on treatment success?

机构信息

Ospedale Papa Giovanni XXIII, Italy.

出版信息

AIDS Rev. 2013 Oct-Dec;15(4):230-6.

PMID:24322383
Abstract

When antiretroviral treatment suppresses HIV RNA levels to below 50 copies/ml, traces of viremia may still be detected with more sensitive assays. In the ARTEMIS trial, 689 antiretroviral treatment-naive patients were randomized to tenofovir/emtricitabine plus either darunavir/ritonavir (n = 343) or lopinavir/ritonavir (n = 346). HIV-1 RNA was evaluated using the Roche Amplicor® Ultrasensitive assay: plasma samples with HIV RNA < 50 copies/ml were classified as either "No HIV RNA detected" (< 5 HIV RNA copies/ml, optical density = background) or HIV RNA detected (5-50 copies/ml). The percentage of patients in each arm with HIV RNA < 5 copies/ml rose progressively from week 2 to week 192. For patients with baseline HIV RNA ≥ 100,000, the percentage with HIV RNA < 5 copies/ml at week 192 was 66% for darunavir/ritonavir and 63% for lopinavir/ritonavir. For patients with baseline HIV RNA < 100,000 copies/ml, the percentage with HIV RNA < 5 copies/ml at week 192 was 79% for darunavir/ritonavir versus 77% for lopinavir/ritonavir. Of the patients on darunavir/ritonavir with HIV RNA < 50 copies/ml, 63% had levels < 5 copies/ml at week 48, versus 80% at week 192. In summary, HIV-1 RNA suppression to < 5 copies/ml is dependent on baseline HIV RNA levels. The HIV RNA levels can remain under quantification limits but still detectable after 2-4 years of antiretroviral treatment.

摘要

当抗逆转录病毒治疗将 HIV RNA 水平抑制到低于 50 拷贝/毫升时,用更敏感的检测方法仍可能检测到微量的病毒血症。在 ARTEMIS 试验中,689 名未经抗逆转录病毒治疗的患者被随机分为替诺福韦/恩曲他滨加达芦那韦/利托那韦(n = 343)或洛匹那韦/利托那韦(n = 346)组。使用罗氏 Amplicor®超敏检测法评估 HIV-1 RNA:HIV RNA < 50 拷贝/毫升的血浆样本分为“未检测到 HIV RNA”(< 5 HIV RNA 拷贝/ml,光密度 = 背景)或 HIV RNA 检测到(5-50 拷贝/ml)。每臂中 HIV RNA < 5 拷贝/ml 的患者比例从第 2 周逐渐增加到第 192 周。对于基线 HIV RNA ≥ 100,000 的患者,在第 192 周时,达芦那韦/利托那韦组和洛匹那韦/利托那韦组中 HIV RNA < 5 拷贝/ml 的患者比例分别为 66%和 63%。对于基线 HIV RNA < 100,000 拷贝/ml 的患者,在第 192 周时,达芦那韦/利托那韦组中 HIV RNA < 5 拷贝/ml 的患者比例为 79%,而洛匹那韦/利托那韦组为 77%。在达芦那韦/利托那韦治疗且 HIV RNA < 50 拷贝/ml 的患者中,有 63%在第 48 周时 HIV RNA 水平 < 5 拷贝/ml,而在第 192 周时为 80%。总之,HIV-1 RNA 抑制到 < 5 拷贝/ml 取决于基线 HIV RNA 水平。在接受抗逆转录病毒治疗 2-4 年后,HIV RNA 水平可能仍低于定量检测下限,但仍可检测到。

相似文献

1
Time to HIV-1 RNA suppression below 5 copies/ml during first-line protease inhibitor-based antiretroviral treatment - any impact of residual viremia on treatment success?一线基于蛋白酶抑制剂的抗逆转录病毒治疗期间 HIV-1 RNA 抑制至<5 拷贝/ml 的时间 - 残余病毒血症对治疗成功有何影响?
AIDS Rev. 2013 Oct-Dec;15(4):230-6.
2
Long-term (96-week) follow-up of antiretroviral-naïve HIV-infected patients treated with first-line lopinavir/ritonavir monotherapy in the MONARK trial.MONARK 试验中一线洛匹那韦/利托那韦单药治疗的初治 HIV 感染患者的长期(96 周)随访。
HIV Med. 2010 Feb;11(2):137-42. doi: 10.1111/j.1468-1293.2009.00752.x. Epub 2009 Aug 13.
3
Once-daily darunavir/ritonavir vs. lopinavir/ritonavir in treatment-naive, HIV-1-infected patients: 96-week analysis.初治的HIV-1感染患者中,每日一次达芦那韦/利托那韦与洛匹那韦/利托那韦的对比:96周分析。
AIDS. 2009 Aug 24;23(13):1679-88. doi: 10.1097/QAD.0b013e32832d7350.
4
Efficacy and safety of once-daily darunavir/ritonavir versus lopinavir/ritonavir in treatment-naive HIV-1-infected patients at week 48.初治的HIV-1感染患者在第48周时,每日一次服用达芦那韦/利托那韦与洛匹那韦/利托那韦的疗效和安全性比较。
AIDS. 2008 Jul 31;22(12):1389-97. doi: 10.1097/QAD.0b013e32830285fb.
5
Virological characterization of patients failing darunavir/ritonavir or lopinavir/ritonavir treatment in the ARTEMIS study: 96-week analysis.ARTEMIS研究中达芦那韦/利托那韦或洛匹那韦/利托那韦治疗失败患者的病毒学特征:96周分析
Antivir Ther. 2011;16(1):99-108. doi: 10.3851/IMP1719.
6
Efficacy and safety of ritonavir-boosted dual protease inhibitor therapy in antiretroviral-naive HIV-1-infected patients: the 2IP ANRS 127 study.利托那韦增强型双蛋白酶抑制剂疗法在初治HIV-1感染患者中的疗效和安全性:2IP ANRS 127研究
J Antimicrob Chemother. 2009 Jul;64(1):118-25. doi: 10.1093/jac/dkp146. Epub 2009 May 6.
7
Characterization of virologic failure patients on darunavir/ritonavir in treatment-experienced patients.对治疗经验丰富的患者中接受达芦那韦/利托那韦治疗的病毒学失败患者的特征进行描述。
AIDS. 2009 Sep 10;23(14):1829-40. doi: 10.1097/QAD.0b013e32832cbcec.
8
Identification of new genotypic cut-off levels to predict the efficacy of lopinavir/ritonavir and darunavir/ritonavir in the TITAN trial.鉴定新基因型界值以预测 TITAN 试验中洛匹那韦/利托那韦和达芦那韦/利托那韦的疗效。
HIV Med. 2009 Nov;10(10):620-6. doi: 10.1111/j.1468-1293.2009.00734.x. Epub 2009 Jul 6.
9
Efficacy and safety of darunavir-ritonavir compared with that of lopinavir-ritonavir at 48 weeks in treatment-experienced, HIV-infected patients in TITAN: a randomised controlled phase III trial.在TITAN研究中,接受过治疗的HIV感染患者中,达芦那韦-利托那韦与洛匹那韦-利托那韦相比在48周时的疗效和安全性:一项随机对照III期试验
Lancet. 2007 Jul 7;370(9581):49-58. doi: 10.1016/S0140-6736(07)61049-6.
10
Pharmacokinetics, efficacy, and safety of darunavir/ritonavir 800/100 mg once-daily in treatment-naïve and -experienced patients.达芦那韦/利托那韦800/100毫克每日一次在初治和经治患者中的药代动力学、疗效及安全性
HIV Clin Trials. 2008 Nov-Dec;9(6):418-27. doi: 10.1310/hct0906-418.

引用本文的文献

1
INSTI-Based Triple Regimens in Treatment-Naïve HIV-Infected Patients Are Associated With HIV-RNA Viral Load Suppression at Ultralow Levels.初治HIV感染患者中基于整合酶链转移抑制剂(INSTI)的三联方案与超低水平的HIV-RNA病毒载量抑制相关。
Open Forum Infect Dis. 2019 Apr 10;6(5):ofz177. doi: 10.1093/ofid/ofz177. eCollection 2019 May.
2
γδ T Cells in HIV Disease: Past, Present, and Future.γδ T 细胞在 HIV 疾病中的作用:过去、现在和未来。
Front Immunol. 2015 Jan 30;5:687. doi: 10.3389/fimmu.2014.00687. eCollection 2014.