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First report of computational protein-ligand docking to evaluate susceptibility to HIV integrase inhibitors in HIV-infected Iranian patients.关于通过计算蛋白-配体对接评估伊朗HIV感染患者对HIV整合酶抑制剂敏感性的首次报告。
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2
First report on molecular docking analysis and drug resistance substitutions to approved HCV NS5A and NS5B inhibitors amongst Iranian patients.伊朗患者获批 HCV NS5A 和 NS5B 抑制剂的分子对接分析和耐药突变的首次报告。
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3
HIV drug resistance among naïve HIV-infected patients in Iran.伊朗初治HIV感染患者中的HIV耐药性。
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4
Resistance to HIV Integrase Inhibitors: About R263K and E157Q Mutations.HIV 整合酶抑制剂耐药性:关于 R263K 和 E157Q 突变。
Viruses. 2018 Jan 18;10(1):41. doi: 10.3390/v10010041.
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Bacterial etiology and antibiotic resistance pattern of septicemia in HIV and non-HIV patients admitted to tertiary care hospitals, Shiraz, South of Iran.伊朗南部设拉子三级护理医院收治的HIV患者和非HIV患者败血症的细菌病因及抗生素耐药模式
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Subtype classification of Iranian HIV-1 sequences registered in the HIV databases, 2006-2013.2006 - 2013年在HIV数据库中登记的伊朗HIV-1序列的亚型分类
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9
Broad antiretroviral activity and resistance profile of the novel human immunodeficiency virus integrase inhibitor elvitegravir (JTK-303/GS-9137).新型人类免疫缺陷病毒整合酶抑制剂埃替格韦(JTK-303/GS-9137)的广泛抗逆转录病毒活性及耐药情况
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Molecular and phylogenetic analysis of HIV-1 variants circulating among injecting drug users in Mashhad-Iran.伊朗马什哈德注射吸毒者中流行的HIV-1变体的分子和系统发育分析。
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伊朗初治HIV感染患者中针对整合酶链转移抑制剂的传播性耐药

Transmitted Drug Resistance Against Integrase Strand Transfer Inhibitors in Iranian HIV-Infected Naïve Patients.

作者信息

Hashempour Ava, Musavi Zahra, Moayedi Javad, Hasanshahi Zahra, Dehghani Behzad, Ghasabi Farzaneh, Joulaei Hassan

机构信息

Shiraz HIV/AIDS Research Center, Institute of Health, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Avicenna J Med Biotechnol. 2023 Jul-Sep;15(3):203-206. doi: 10.18502/ajmb.v15i3.12931.

DOI:10.18502/ajmb.v15i3.12931
PMID:37538237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10395453/
Abstract

BACKGROUND

Human Immunodeficiency Virus (HIV) has claimed the lives of millions of people during the past decades. While several antiretroviral drugs like Integrase Strand Transfer Inhibitors (INSTIs) have been introduced to control HIV, Transmitted Drug Resistance (TDR) in HIV genome caused failure in treatment. This study aimed to investigate TDR and natural occurring mutations (NOPs) in HIV integrase gene in Iranian HIV patients.

METHODS

In this cross-sectional study, blood samples of 30 HIV-positive patients who had never taken integrase inhibitors were considered for CD4 T cell count, RT real-time PCR, and, Nested PCR. The sequencing results were analyzed by CLC sequence viewer software and Stanford University HIV Drug Resistance Database.

RESULTS

In all samples, nine NOPs with a high prevalence were found; however, we did not find any drug resistance mutations, except for a mutation in one sample, which showed a low resistance level. Subtype A1 was dominant in all samples.

CONCLUSION

Based on the findings and compared to our previous study, all patients were sustainable to main integrase inhibitors, including bictegravir, raltegravir, bictegravir, elvitegravir and dolutegravir. It seems the resistant mutation pattern attributed to integrase inhibitors was not diffent among studied patients; hence, the prescription of such inhibitors helps physicians to control HIV infection in Iranian HIV-infected patients.

摘要

背景

在过去几十年中,人类免疫缺陷病毒(HIV)已夺去数百万人的生命。虽然已引入多种抗逆转录病毒药物,如整合酶链转移抑制剂(INSTIs)来控制HIV,但HIV基因组中的传播性耐药(TDR)导致治疗失败。本研究旨在调查伊朗HIV患者HIV整合酶基因中的TDR和自然发生的突变(NOPs)。

方法

在这项横断面研究中,对30名从未服用过整合酶抑制剂的HIV阳性患者的血样进行CD4 T细胞计数、RT实时PCR和巢式PCR检测。测序结果通过CLC序列查看软件和斯坦福大学HIV耐药数据库进行分析。

结果

在所有样本中,发现了9种高流行率的NOPs;然而,除了一个样本中的一个突变显示出低耐药水平外,我们未发现任何耐药突变。A1亚型在所有样本中占主导地位。

结论

基于这些发现并与我们之前的研究相比,所有患者对主要的整合酶抑制剂,包括比克替拉韦、拉替拉韦、比克替拉韦、埃替拉韦和多替拉韦均具有耐受性。似乎整合酶抑制剂导致的耐药突变模式在研究患者中并无差异;因此,此类抑制剂的处方有助于医生控制伊朗HIV感染患者的HIV感染。