AI Article Synopsis

  • The study investigates the mutational load of drug resistance and APOBEC editing in heavily treatment-experienced (HTE) individuals with multidrug-resistant HIV, which had not been previously explored.
  • Researchers analyzed HIV-DNA and HIV-RNA mutations in 20 patients using next-generation sequencing, finding high levels of both types of viral loads and complex resistance patterns.
  • Results indicate that certain drug-resistant mutations are prevalent in these patients, with implications for identifying those at greater risk of treatment failure, particularly when comparing DNA and RNA mutations along with APOBEC editing effects.

Article Abstract

Background: The impact of drug resistance mutational load and APOBEC editing in heavily treatment-experienced (HTE) people living with multidrug-resistant HIV has not been investigated.

Material And Methods: This study explored the HIV-DNA and HIV-RNA mutational load of drug resistance and APOBEC-related mutations through next-generation sequencing (NGS, Illumina MiSeq) in 20 failing HTE participants enrolled in the PRESTIGIO registry.

Results: The patients showed high levels of both HIV-DNA (4.5 [4.0-5.2] log copies/10 T-CD4+ cell) and HIV-RNA (4.5 [4.1-5.0] log copies/mL) with complex resistance patterns in both compartments. Among the 255 drug-resistant mutations found, 66.3% were concordantly detected in both HIV-DNA and HIV-RNA; 71.3% of mutations were already present in historical Sanger genotypes. At an intra-patient frequency > 5%, a considerable proportion of mutations detected through DNA-NGS were found in historical genotypes but not through RNA-NGS, and few patients had APOBEC-related mutations. Of 14 patients who switched therapy, the five who failed treatment had DNA resistance with higher intra-patient frequency and higher DNA/RNA mutational load in a context of tendentially less pronounced APOBEC editing compared with those who responded.

Conclusions: Using NGS in HIV-DNA and HIV-RNA together with APOBEC editing evaluation might help to identify HTE individuals with MDR who are more prone to experience virological failure.

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http://dx.doi.org/10.1016/j.ijantimicag.2021.106492DOI Listing

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