Response to HAART in French patients with resistant HIV-1 treated at primary infection: ANRS Resistance Network

Author:

Chaix Marie-Laure1,Desquilbet Loic2,Descamps Diane3,Costagliola Dominique45,Deveau Christiane2,Galimand Julie1,Goujard Cécile6,Signori-Schmuck Anne7,Schneider Veronique8,Tamalet Catherine9,Pellegrin Isabelle10,Wirden Marc11,Masquelier Bernard10,Brun-Vezinet Francoise3,Rouzioux Christine1,Meyer Laurence2,

Affiliation:

1. EA 3620, Université Paris Descartes, Service de Virologie, CHU Necker-Enfants Malades, Paris, France

2. Inserm, U822, IFR69, Le Kremlin-Bicêtre; Université Paris-Sud, Faculté de Médecine Paris-Sud, Le Kremlin-Bicêtre; AP-HP, Hopital Bicêtre, Service de Santé Publique, Le Kremlin Bicêtre, France

3. Service de Virologie, CHU Bichat-Claude Bernard, Paris, France

4. INSERM U 720, Paris, France

5. Université Pierre et Marie Curie-Paris 6, Paris, France

6. Service de Médecine Interne, Le Kremlin-Bicêtre, France

7. Service de Virologie, CHU Nord, Grenoble, France

8. Service de Virologie, CHU Tenon, Paris, France

9. Service de Virologie, CHU La Timone, Marseille, France

10. Service de Virologie, CHU Pellegrin, Bordeaux, France

11. Service de Virologie, CHU Pitié-Salpétrière, Paris, France

Abstract

Objective The aim of the study was to analyse the response to highly active antiretroviral therapy (HAART) initiated at the time of primary HIV infection (PHI) in patients infected with a virus resistant to ≥1 drug of their treatment compared with patients infected with a wild-type virus. Methods We analysed data from 350 patients who were enrolled from 1996–2004 in the French ANRS PRIMO Cohort or in the ANRS Resistance Group and treated with HAART during PHI. During the study period, HAART was initiated before the result of the genotypic resistance test was available. We compared patients infected with a virus resistant to ≥1 drug of their regimen (GR group, n=46) with patients harbouring a wild-type virus (WT group, n=304). Virological and immunological response to treatment according to drug-resistance profile was analysed 3 months and 6 months after HAART initiation. Results In GR and WT groups, HIV RNA level was <400 copies/ml in 68% and 83% ( P=0.02) and <50 copies/ml in 23% and 40% ( P=0.08) 3 months after HAART initiation. In multivariable logistic regression taking into account gender, age, boosted PI regimen, plasma HIV RNA and CD4+ T-cell count at HAART initiation, patients with virus resistant to ≥1 drug of their regimen were significantly less likely to achieve undetectable viral load at month 3 (odds ratio 0.32, 95% confidence interval 0.15–0.72) than the others. This difference was sustained up to month 6. Conclusion In this large cohort of HAART-treated PHI-patients, the presence of drug resistance mutations led to suboptimal response to early therapy.

Publisher

SAGE Publications

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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