Journal Article

Dolutegravir-associated resistance mutations after first-line treatment failure in Brazil

Hunter, James R., Camargo, Michelle, Dias, Danilo, de Lima, Isaac Barbosa, Diaz, Ricardo Sobhie, Schechter, Mauro, Nassar, Isabela, Galinskas, Juliana, Caldeira, Debora Bellini, Sucupira, Maria Cecilia

2023

Overview

Background Since January 2017, the recommended first-line antiretroviral regimen in Brazil is the fixed-dose combination of tenofovir plus lamivudine with dolutegravir (TL + D). According to the literature, integrase resistance-associated mutations (INRAMs) are rarely found upon virologic failure to first-line dolutegravir plus two nucleoside reverse transcriptase inhibitors. We evaluated the HIV antiretroviral genotypic resistance profile of patients referred for genotyping in the public health system who failed first-line TL + D after at least six months of therapy on or before December 31, 2018. Methods HIV Sanger sequences of the pol gene were generated from plasma of patients with confirmed virologic failure to first-line TL + D in the Brazilian public health system before December 31, 2018. Results One hundred thirteen individuals were included in the analysis. Major INRAMs were detected in seven patients (6.19%), four with R263K, one with G118R, one with E138A, and one with G140R. Four patients with major INRAMs also had the K70E and M184V mutations in the RT gene. Sixteen (14.2%) additional individuals presented minor INRAMs, and five (4,42%) patients had both major and minor INRAMS. Thirteen (11.5%) patients also presented mutations in the RT gene selected by tenofovir and lamivudine, including four with both the K70E and M184V mutations and four with only M184V. The integrase mutations L101I and T124A, which are in the in vitro pathway for integrase inhibitor resistance, were found in 48 and 19 patients, respectively. Mutations not related to TL + D, thus probable transmitted resistance mutations (TDR), were present in 28 patients (24.8%): 25 (22.1%) to nucleoside reverse transcriptase inhibitors, 19 (16.8%) to non-nucleoside reverse transcriptase inhibitors, and 6 (5.31%) to protease inhibitors. Conclusions In marked contrast to previous reports, we report a relatively high frequency of INRAMs among selected patients failing first-line TL + D in the public health system in Brazil. Possible reasons for this discrepancy include delays in detecting virologic failure, patients inadvertently on dolutegravir monotherapy, TDR, and/or infecting subtype.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Analysis / Anti-Retroviral Agents / Antiretroviral agents / Antiretroviral drugs / Brazil / Dolutegravir / Drug interactions / Drug resistance / Drug therapy / Failure / Genotyping / HIV / HIV infection / HIV Infections - drug therapy / Human immunodeficiency virus / Humans / Infectious Diseases / Integrase / Internal Medicine / Laboratories / Lamivudine / Lamivudine - pharmacology / Lamivudine - therapeutic use / Lymphocytes / Medical Microbiology / Medicine / Medicine & Public Health / Mutation / Non-nucleoside reverse transcriptase inhibitors / Nucleoside reverse transcriptase inhibitors / Nucleosides / Parasitology / Patients / Pol gene / Protease inhibitors / Proteinase inhibitors / Public health / Research Article / Resistance associated mutations / Reverse Transcriptase Inhibitors - pharmacology / Reverse Transcriptase Inhibitors - therapeutic use / RNA-directed DNA polymerase / Tenofovir / Transmitted drug resistance / Treatment Failure / Tropical Medicine / Virologic failure