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Usefulness of Integrase resistance testing in proviral HIV-1 DNA in patients with Raltegravir prior failure.

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Fernández-Caballero JÁ, Chueca N, Álvarez M, Mérida MD, López J, Sánchez JA, Vinuesa D, Martínez MÁ, Hernández J, García F,


Fernández-Caballero JÁ, Chueca N, Álvarez M, Mérida MD, López J, Sánchez JA, Vinuesa D, Martínez MÁ, Hernández J, García F, (click to view)

Fernández-Caballero JÁ, Chueca N, Álvarez M, Mérida MD, López J, Sánchez JA, Vinuesa D, Martínez MÁ, Hernández J, García F,

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BMC infectious diseases 2016 5 1316(1) 197

Abstract
BACKGROUND
In our study, we have hypothesized that proviral DNA may show the history of mutations that emerged at previous failures to a Raltegravir containing regimen, in patients who are currently undetectable and candidates to simplification to a Dolutegravir containing regimen, in order to decide on once a day or twice a day dosing.

METHODS
We have performed a pilot, observational, retrospective, non interventional study, including 7 patients infected by HIV-1, all with a history of previous failure to a RAL containing regimen, that were successfully salvaged and had reached viral suppression. A genotypic viral Integrase region study was available for each patient at the moment of RAL failure. After an average (IQR) time of 48 months (29-53) Integrase resistance mutations in proviral DNA were studied.

RESULTS
All the patients were infected by HIV-1 B subtypes, with a mean age of 55 (range 43 to 56), originating from Spain, and 4 were women. Median viral load (log) and CD4 count at the moment of the study on proviral DNA was of 1.3 log cp/ml (range 0-1.47) and 765.5 cells/μL (range; 436.75-1023.75). The median time (IQR) between previous failure to RAL and the study on proviral DNA was 48 (29-53) months. At Raltegravir failure, N155H was detected in four patients, and other secondary mutations were detected in five patients (71.4 %). In proviral DNA, N155H was detected by population sequencing in three patients (42.8 %), and UDS demonstrated a 9.77 % relative abundance of N155H in the remaining patient. Sanger sequencing correctly identified all the secondary mutations.

CONCLUSION
This is a pilot study that demonstrates the possibility of properly identifying N155H and some secondary mutations 29-53 months after failure.

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