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Drug Resistance to HIV-1 Integrase Inhibitors Among Treatment-Naive Patients in Beijing, China
INTRODUCTION: Integrase strand transfer inhibitors (INSTIs) are important drugs that are currently used as the first line treatment for HIV-1 patients. The aim of this study was to characterize HIV-1 INSTI mutations among ART-naive patients in Beijing from 2019–2021. METHODS: 865 ART-naive patients...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8922317/ https://www.ncbi.nlm.nih.gov/pubmed/35300056 http://dx.doi.org/10.2147/PGPM.S345797 |
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author | Yu, Fengting Li, Qun Wang, Linghang Zhao, Hongxin Wu, Hao Yang, Siyuan Tang, Yunxia Xiao, Jiang Zhang, Fujie |
author_facet | Yu, Fengting Li, Qun Wang, Linghang Zhao, Hongxin Wu, Hao Yang, Siyuan Tang, Yunxia Xiao, Jiang Zhang, Fujie |
author_sort | Yu, Fengting |
collection | PubMed |
description | INTRODUCTION: Integrase strand transfer inhibitors (INSTIs) are important drugs that are currently used as the first line treatment for HIV-1 patients. The aim of this study was to characterize HIV-1 INSTI mutations among ART-naive patients in Beijing from 2019–2021. METHODS: 865 ART-naive patients were enrolled in this study between January 2019 and June 2021 in Beijing. The amplification of the entire pol gene containing the reverse transcriptase, protease and integrase regions was performed using a validated In-house SBS method. HIV-1 subtypes and circulating recombinant forms (CRFs) were determined using the COMET online tool (http://comet.retrovirology.lu). Stanford HIV-1 drug resistance database (HIVdb version 8.9) was used to analyze the mutations. RESULTS: 865 HIV-1 pol sequences were successfully amplified and sequenced. Among them, no major INSTI-related mutations were identified, but 12 polymorphic accessory mutations were found. Two patients have E138A and G163R mutations respectively and both could cause low-level resistance to RAL and EVG. Furthermore, one patient having S230R mutation resulted in low-level resistance to RAL, EVG, DTG and BIC. CONCLUSION: The prevalence of INSTIs mutations remains low, which demonstrated that INSTIs have good applicability currently in our city. Nevertheless, it is very important to monitor the INSTI-related mutations in Beijing. |
format | Online Article Text |
id | pubmed-8922317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-89223172022-03-16 Drug Resistance to HIV-1 Integrase Inhibitors Among Treatment-Naive Patients in Beijing, China Yu, Fengting Li, Qun Wang, Linghang Zhao, Hongxin Wu, Hao Yang, Siyuan Tang, Yunxia Xiao, Jiang Zhang, Fujie Pharmgenomics Pers Med Original Research INTRODUCTION: Integrase strand transfer inhibitors (INSTIs) are important drugs that are currently used as the first line treatment for HIV-1 patients. The aim of this study was to characterize HIV-1 INSTI mutations among ART-naive patients in Beijing from 2019–2021. METHODS: 865 ART-naive patients were enrolled in this study between January 2019 and June 2021 in Beijing. The amplification of the entire pol gene containing the reverse transcriptase, protease and integrase regions was performed using a validated In-house SBS method. HIV-1 subtypes and circulating recombinant forms (CRFs) were determined using the COMET online tool (http://comet.retrovirology.lu). Stanford HIV-1 drug resistance database (HIVdb version 8.9) was used to analyze the mutations. RESULTS: 865 HIV-1 pol sequences were successfully amplified and sequenced. Among them, no major INSTI-related mutations were identified, but 12 polymorphic accessory mutations were found. Two patients have E138A and G163R mutations respectively and both could cause low-level resistance to RAL and EVG. Furthermore, one patient having S230R mutation resulted in low-level resistance to RAL, EVG, DTG and BIC. CONCLUSION: The prevalence of INSTIs mutations remains low, which demonstrated that INSTIs have good applicability currently in our city. Nevertheless, it is very important to monitor the INSTI-related mutations in Beijing. Dove 2022-03-10 /pmc/articles/PMC8922317/ /pubmed/35300056 http://dx.doi.org/10.2147/PGPM.S345797 Text en © 2022 Yu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Yu, Fengting Li, Qun Wang, Linghang Zhao, Hongxin Wu, Hao Yang, Siyuan Tang, Yunxia Xiao, Jiang Zhang, Fujie Drug Resistance to HIV-1 Integrase Inhibitors Among Treatment-Naive Patients in Beijing, China |
title | Drug Resistance to HIV-1 Integrase Inhibitors Among Treatment-Naive Patients in Beijing, China |
title_full | Drug Resistance to HIV-1 Integrase Inhibitors Among Treatment-Naive Patients in Beijing, China |
title_fullStr | Drug Resistance to HIV-1 Integrase Inhibitors Among Treatment-Naive Patients in Beijing, China |
title_full_unstemmed | Drug Resistance to HIV-1 Integrase Inhibitors Among Treatment-Naive Patients in Beijing, China |
title_short | Drug Resistance to HIV-1 Integrase Inhibitors Among Treatment-Naive Patients in Beijing, China |
title_sort | drug resistance to hiv-1 integrase inhibitors among treatment-naive patients in beijing, china |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8922317/ https://www.ncbi.nlm.nih.gov/pubmed/35300056 http://dx.doi.org/10.2147/PGPM.S345797 |
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