Integrase strand transfer inhibitors resistance-associated mutations in HIV-infected pregnant women

0Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

Abstract

Objective. To date, no data exist regarding the prevalence of integrase inhibitor (INSTI) resistance-associated mutations (HIVDRM) in HIV-infected pregnant women (HPW) in Latin America. We describe the prevalence and transmissibility of in-tegrase HIVDRM in a historical cohort of INSTI-naïve HPW from Argentina (n=56) with Next Generation Sequencing (NGS). Material and methods. Bioinformatics analysis was performed by HyDRA software for 20%, 10%, 5%, 2%, and 1% sensitivity thresholds. We calculated the mutational viral load for each INSTI-HIVDRM, considering those with >1000 c/mL as of high risk of transmissibility. Results. The predominant HIV subtype was BF (78.5%). Major HIVDRM were not detected with the population sequencing 20% filter. With a 1% threshold, the prevalence in-creased to 8.9%; Y143C/S, E92G, E138K, and T66I mutations were found. The median (range) mutational load (expressed in c/mL) was: 355 (50.2-11705); with only 1 case >1000 c/mL Accessory mutations (G163R/K, T97A) were detected mostly with a 20% sensitivity threshold with an overall prevalence of 23.2%; the median (IQR) mutational load was: 23929 (4009-63158) c/mL; all of them above 1000 c/mL. Conclusion. Our results show evidence of the presence of major INSTI-HIVDRM as aleatory mutations and a high fre-quency of accessory mutations with potential transmissibility in HPW.

Cite

CITATION STYLE

APA

Cecchini, D., Sfalcin, J., Zapiola, I., Gomez, A., Fernandez-Giuliano, S., Rodriguez, C., … Bouzas, M. B. (2024). Integrase strand transfer inhibitors resistance-associated mutations in HIV-infected pregnant women. Revista Espanola de Quimioterapia, 37(6), 479–485. https://doi.org/10.37201/req/074.2024

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free