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Infection. 2017 Apr;45(2):165-170. doi: 10.1007/s15010-016-0936-5. Epub 2016 Aug 16.
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Polymorphic substitution E157Q in HIV-1 integrase increases R263K-mediated dolutegravir resistance and decreases DNA binding activity.HIV-1整合酶中的多态性替代E157Q增加了R263K介导的多替拉韦耐药性并降低了DNA结合活性。
J Antimicrob Chemother. 2016 Aug;71(8):2083-8. doi: 10.1093/jac/dkw109. Epub 2016 Apr 15.
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Effect of dolutegravir functional monotherapy on HIV-1 virological response in integrase strand transfer inhibitor resistant patients.多替拉韦功能单药疗法对整合酶链转移抑制剂耐药患者的HIV-1病毒学应答的影响。
Antivir Ther. 2016;21(6):481-488. doi: 10.3851/IMP3033. Epub 2016 Feb 11.
5
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6
Lack of resistance to integrase inhibitors among antiretroviral-naive subjects with primary HIV-1 infection, 2007-2013.2007 - 2013年原发性HIV - 1感染的初治抗逆转录病毒治疗受试者中对整合酶抑制剂缺乏耐药性
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韩国初治患者中整合酶抑制剂耐药突变的前瞻性观察研究。

Integrase Strand Transfer Inhibitor Resistance Mutations in Antiretroviral Treatment-naïve Patients in Korea: a Prospective, Observational Study.

机构信息

Center for Infectious Diseases Research, Department of Internal Medicine, National Medical Center, Seoul, Korea.

出版信息

J Korean Med Sci. 2018 May 14;33(25):e173. doi: 10.3346/jkms.2018.33.e173. eCollection 2018 Jun 18.

DOI:10.3346/jkms.2018.33.e173
PMID:29915524
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6000596/
Abstract

The present study investigated prevalence of integrase strand transfer inhibitors (INSTI) resistance mutations in HIV-1-infected antiretroviral therapy (ART)-naïve patients in Korea. From 106 plasma samples, amplification and sequencing of integrase genes was performed, and major or minor mutations were calculated by the Stanford HIV drug resistance mutation interpretation algorithm. No major INSTI resistance mutations were found, and 14 minor mutations were detected in 13 (12.3%) patients. The present data support the recommendation that routine testing for INSTI resistance mutations before starting ART is not necessary.

摘要

本研究调查了韩国未经抗逆转录病毒治疗 (ART) 的 HIV-1 感染患者中整合酶链转移抑制剂 (INSTI) 耐药突变的流行情况。从 106 份血浆样本中,对整合酶基因进行了扩增和测序,并通过斯坦福 HIV 耐药突变解释算法计算了主要或次要突变。未发现主要的 INSTI 耐药突变,在 13 名 (12.3%)患者中检测到 14 种次要突变。本数据支持在开始 ART 之前常规检测 INSTI 耐药突变并非必要的建议。