Human Immunodeficiency Virus-1 Drug Resistance Mutations in Iranian Treatment-experienced Individuals

Author:

Bokharaei-Salim Farah1ORCID,Khanaliha Khadijeh2ORCID,Monavari Seyed Hamidreza1,Kiani Seyed Jalal1,Tavakoli Ahmad12,jafari Ensieh3,Chavoshpour Sara1,Razizadeh Mohammad Hossein1,Kalantari Saeed4

Affiliation:

1. Department of Virology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran

2. Research Center of Pediatric Infectious Diseases, Institute of Immunology and Infectious Diseases, Iran University of Medical Sciences, Tehran, Iran

3. Department of Biology, Faculty of Basic Sciences, Noor Danesh University, Isfahan, Iran

4. Departments of Infectious Diseases and Tropical Medicine, Iran University of Medical Sciences, Tehran, Iran

Abstract

Background: Human immunodeficiency virus-1 infection still remains a global health threat. While antiretroviral therapy is the primary treatment option, concerns about the emergence of drug-resistance mutations and treatment failure in HIV-infected patients persist. Objective: In this study, we investigated the development of drug resistance in HIV-1-infected individuals receiving antiretroviral therapy for 6-10 years. Methods: In this cross-sectional study, we evaluated 144 people living with HIV-1 who had received antiretroviral therapy for at least 6 years. Plasma specimens were collected, and the HIV-1 viral load and drug-resistance mutations were assessed using molecular techniques. Results: The demographic and epidemiological characteristics of the participants were also analyzed: Twelve [8.3%) of the studied patients showed a viral load over 1000 copies per/mL, which indicates the suboptimal response to antiretroviral therapy. Significant correlations were found between viral load and CD4 count, as well as epidemiological factors, such as vertical transmission, history of imprisonment, and needle stick injuries. Drug resistance mutations were detected in 10 (83.3%) of patients who failed on antiretroviral therapy, with the most common mutations observed against nucleoside reverse transcriptase inhibitors (5 (41.7%)) and non-nucleoside reverse transcriptase inhibitors (9 (75%)). Phylogenetic analysis revealed that 12 patients who failed treatment were infected with CRF35_AD. Conclusion: Our study provides important insights into the characteristics and development of drug resistance in HIV-1-infected individuals receiving long-term antiretroviral therapy in Iran. The findings underline the need for regular viral load monitoring, individualized treatment selection, and targeted interventions to optimize treatment outcomes and prevent the further spread of drug-resistant strains.

Funder

Research Deputy of Iran University of Medical Sciences, Tehran, Iran

Publisher

Bentham Science Publishers Ltd.

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