Phenotypic analysis of HIV-1 E157Q integrase polymorphism and impact on virological outcome in patients initiating an integrase inhibitor-based regimen

To assess the phenotypic susceptibility of the E157Q polymorphism in HIV-1 integrase (IN) and the virological outcome of patients infected with E157Q-mutated virus initiating an IN inhibitor (INI)-based regimen. This was a multicentre study assessing IN sequences from INI-naive patients among 17 Fre...

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Veröffentlicht in:Journal of antimicrobial chemotherapy 2018-04, Vol.73 (4), p.1039-1044
Hauptverfasser: Charpentier, Charlotte, Malet, Isabelle, Andre-Garnier, Elisabeth, Storto, Alexandre, Bocket, Laurence, Amiel, Corinne, Morand-Joubert, Laurence, Tumiotto, Camille, Nguyen, Thuy, Maillard, Anne, Rodallec, Audrey, Leoz, Marie, Montes, Brigitte, Schneider, Véronique, Plantier, Jean-Christophe, Dina, Julia, Pallier, Coralie, Mirand, Audrey, Roussel, Catherine, Signori-Schmuck, Anne, Raymond, Stéphanie, Calvez, Vincent, Delaugerre, Constance, Marcelin, Anne-Geneviève, Descamps, Diane
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Sprache:eng
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Zusammenfassung:To assess the phenotypic susceptibility of the E157Q polymorphism in HIV-1 integrase (IN) and the virological outcome of patients infected with E157Q-mutated virus initiating an IN inhibitor (INI)-based regimen. This was a multicentre study assessing IN sequences from INI-naive patients among 17 French HIV clinical centres. E157Q site-directed mutants in pNL4.3 and pCRF02_AG contexts were assessed in a recombinant phenotypic assay. Prevalence of the E157Q polymorphism was 2.7% among 8528 IN sequences from INI-naive patients and its distribution was 1.7%, 5.6% and 2.2% in B, CRF02_AG and various non-B subtypes, respectively. Thirty-nine INI-naive patients with E157Q-mutated virus initiated an INI-based regimen. Among them, 15 had a viral load (VL)  50 copies/mL at the time of INI-based regimen initiation. Among them eight were receiving a first-line regimen and the only two patients who did not reach VL 
ISSN:0305-7453
1460-2091
DOI:10.1093/jac/dkx511