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

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 failur...

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Autores principales: Hashempour, Ava, Musavi, Zahra, Moayedi, Javad, Hasanshahi, Zahra, Dehghani, Behzad, Ghasabi, Farzaneh, Joulaei, Hassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Avicenna Research Institute 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395453/
https://www.ncbi.nlm.nih.gov/pubmed/37538237
http://dx.doi.org/10.18502/ajmb.v15i3.12931
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author Hashempour, Ava
Musavi, Zahra
Moayedi, Javad
Hasanshahi, Zahra
Dehghani, Behzad
Ghasabi, Farzaneh
Joulaei, Hassan
author_facet Hashempour, Ava
Musavi, Zahra
Moayedi, Javad
Hasanshahi, Zahra
Dehghani, Behzad
Ghasabi, Farzaneh
Joulaei, Hassan
author_sort Hashempour, Ava
collection PubMed
description 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.
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spelling pubmed-103954532023-08-03 Transmitted Drug Resistance Against Integrase Strand Transfer Inhibitors in Iranian HIV-Infected Naïve Patients Hashempour, Ava Musavi, Zahra Moayedi, Javad Hasanshahi, Zahra Dehghani, Behzad Ghasabi, Farzaneh Joulaei, Hassan Avicenna J Med Biotechnol Short Communication 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. Avicenna Research Institute 2023 /pmc/articles/PMC10395453/ /pubmed/37538237 http://dx.doi.org/10.18502/ajmb.v15i3.12931 Text en Copyright© 2023 Avicenna Research Institute https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Short Communication
Hashempour, Ava
Musavi, Zahra
Moayedi, Javad
Hasanshahi, Zahra
Dehghani, Behzad
Ghasabi, Farzaneh
Joulaei, Hassan
Transmitted Drug Resistance Against Integrase Strand Transfer Inhibitors in Iranian HIV-Infected Naïve Patients
title Transmitted Drug Resistance Against Integrase Strand Transfer Inhibitors in Iranian HIV-Infected Naïve Patients
title_full Transmitted Drug Resistance Against Integrase Strand Transfer Inhibitors in Iranian HIV-Infected Naïve Patients
title_fullStr Transmitted Drug Resistance Against Integrase Strand Transfer Inhibitors in Iranian HIV-Infected Naïve Patients
title_full_unstemmed Transmitted Drug Resistance Against Integrase Strand Transfer Inhibitors in Iranian HIV-Infected Naïve Patients
title_short Transmitted Drug Resistance Against Integrase Strand Transfer Inhibitors in Iranian HIV-Infected Naïve Patients
title_sort transmitted drug resistance against integrase strand transfer inhibitors in iranian hiv-infected naïve patients
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395453/
https://www.ncbi.nlm.nih.gov/pubmed/37538237
http://dx.doi.org/10.18502/ajmb.v15i3.12931
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