Suppr超能文献

在临床开发期间,对参与者中发现的多伟拉韦耐药模式进行综述。

Review of Doravirine Resistance Patterns Identified in Participants During Clinical Development.

机构信息

Departments of Clinical Research.

Infectious Disease and Vaccine Research; and.

出版信息

J Acquir Immune Defic Syndr. 2020 Dec 15;85(5):635-642. doi: 10.1097/QAI.0000000000002496.

Abstract

BACKGROUND

Doravirine (DOR) is a novel non-nucleoside reverse transcriptase inhibitor (NNRTI) approved for the treatment of HIV-1 infection in patients with no known DOR resistance-associated mutations. DOR was rationally designed to address limitations associated with other approved NNRTIs, particularly resistance from common NNRTI resistance-associated mutants containing K103N, Y181C, or G190A reverse transcriptase substitutions.

SETTING

Data to date from both in vitro studies and clinical trials have been compiled to summarize the resistance profile of DOR.

METHODS

We analyzed data from in vitro studies and phase 2 and 3 trials to assess the emergence of resistance-associated mutations and their impact on efficacy among participants treated with DOR.

RESULTS

DOR exhibited a distinct resistance profile compared with efavirenz and rilpivirine in vitro and in vivo; mutant viruses that were resistant to DOR showed limited cross-resistance to efavirenz and rilpivirine. In clinical trials, the development of DOR resistance-associated substitutions in reverse transcriptase was uncommon.

CONCLUSION

Overall, minimal cross-resistance across NNRTIs was observed for DOR and limited development of DOR-related resistance. These data should assist clinicians in further understanding the resistance profile of DOR, so appropriate treatment decisions can be made for their patients.

摘要

背景

多伟拉韦(DOR)是一种新型非核苷类逆转录酶抑制剂(NNRTI),获批用于治疗无已知 DOR 耐药相关突变的 HIV-1 感染患者。DOR 是经过合理设计的,旨在解决其他已批准的 NNRTI 存在的局限性,尤其是针对常见 NNRTI 耐药相关突变体(包含 K103N、Y181C 或 G190A 逆转录酶取代)引起的耐药问题。

设定

目前已汇总了来自体外研究和临床试验的数据,以总结 DOR 的耐药谱。

方法

我们分析了来自体外研究和 2 期和 3 期临床试验的数据,以评估 DOR 治疗参与者中耐药相关突变的出现及其对疗效的影响。

结果

与体外和体内的依非韦伦和利匹韦林相比,DOR 表现出独特的耐药谱;对 DOR 耐药的突变病毒对依非韦伦和利匹韦林的交叉耐药性有限。在临床试验中,逆转录酶中 DOR 耐药相关取代的出现并不常见。

结论

总体而言,DOR 与 NNRTI 之间交叉耐药性最小,与 DOR 相关的耐药性发展有限。这些数据应有助于临床医生进一步了解 DOR 的耐药谱,以便为患者做出适当的治疗决策。

相似文献

1
Review of Doravirine Resistance Patterns Identified in Participants During Clinical Development.
J Acquir Immune Defic Syndr. 2020 Dec 15;85(5):635-642. doi: 10.1097/QAI.0000000000002496.
2
Prevalence of predicted resistance to doravirine in HIV-1-positive patients after exposure to non-nucleoside reverse transcriptase inhibitors.
Int J Antimicrob Agents. 2019 Apr;53(4):515-519. doi: 10.1016/j.ijantimicag.2019.02.007. Epub 2019 Feb 12.
3
Doravirine Suppresses Common Nonnucleoside Reverse Transcriptase Inhibitor-Associated Mutants at Clinically Relevant Concentrations.
Antimicrob Agents Chemother. 2016 Mar 25;60(4):2241-7. doi: 10.1128/AAC.02650-15. Print 2016 Apr.
4
Rilpivirine and Doravirine Have Complementary Efficacies Against NNRTI-Resistant HIV-1 Mutants.
J Acquir Immune Defic Syndr. 2016 Aug 15;72(5):485-91. doi: 10.1097/QAI.0000000000001031.
5
6
Doravirine responses to HIV-1 viruses bearing mutations to NRTIs and NNRTIs under in vitro selective drug pressure.
J Antimicrob Chemother. 2023 Aug 2;78(8):1921-1928. doi: 10.1093/jac/dkad184.
7
Doravirine: a new non-nucleoside reverse transcriptase inhibitor for the treatment of HIV infection.
Drugs Today (Barc). 2020 Feb;56(2):113-124. doi: 10.1358/dot.2020.56.2.3109966.
8
Low prevalence of doravirine-associated resistance mutations among polish human immunodeficiency-1 (HIV-1)-infected patients.
Antivir Ther. 2021 May;26(3-5):69-78. doi: 10.1177/13596535211043044. Epub 2021 Oct 20.
10
Rational Design of Doravirine: From Bench to Patients.
ACS Infect Dis. 2020 Jan 10;6(1):64-73. doi: 10.1021/acsinfecdis.9b00178. Epub 2019 Dec 19.

引用本文的文献

4
Comprehensive database of HIV mutations selected during antiretroviral in vitro passage experiments.
Antiviral Res. 2024 Oct;230:105988. doi: 10.1016/j.antiviral.2024.105988. Epub 2024 Aug 16.
5
HIV-1 transmitted drug resistance in newly diagnosed individuals in Italy over the period 2015-21.
J Antimicrob Chemother. 2024 Sep 3;79(9):2152-2162. doi: 10.1093/jac/dkae189.
8
Recommendations on data sharing in HIV drug resistance research.
PLoS Med. 2023 Sep 22;20(9):e1004293. doi: 10.1371/journal.pmed.1004293. eCollection 2023 Sep.
9
Doravirine/Lamivudine/Tenofovir Disoproxil Fumarate for Nonoccupational HIV-1 Postexposure Prophylaxis: A Prospective Open-Label Trial (DORAVIPEP).
Open Forum Infect Dis. 2023 Jul 19;10(8):ofad374. doi: 10.1093/ofid/ofad374. eCollection 2023 Aug.

本文引用的文献

3
Rational Design of Doravirine: From Bench to Patients.
ACS Infect Dis. 2020 Jan 10;6(1):64-73. doi: 10.1021/acsinfecdis.9b00178. Epub 2019 Dec 19.
7
HIV subtype diversity worldwide.
Curr Opin HIV AIDS. 2019 May;14(3):153-160. doi: 10.1097/COH.0000000000000534.
8
Prevalence of predicted resistance to doravirine in HIV-1-positive patients after exposure to non-nucleoside reverse transcriptase inhibitors.
Int J Antimicrob Agents. 2019 Apr;53(4):515-519. doi: 10.1016/j.ijantimicag.2019.02.007. Epub 2019 Feb 12.
9
Rare occurrence of doravirine resistance-associated mutations in HIV-1-infected treatment-naive patients.
J Antimicrob Chemother. 2019 Mar 1;74(3):614-617. doi: 10.1093/jac/dky464.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验