Comparative Immunovirological and Clinical Responses to Antiretroviral Therapy Between HIV-1 Group O and HIV-1 Group M Infected Patients

Author:

Kouanfack Charles1,Unal Guillemette2,Schaeffer Laura3,Kfutwah Anfumbom4,Aghokeng Avelin5,Mougnutou Rose1,Tchemgui-Noumsi Nathalie1,Alessandri-Gradt Elodie2,Delaporte Eric5,Simon François6,Vray Muriel3,Plantier Jean-Christophe2ORCID,Alima Michèle,Essengué Lucie,Mounpou Georges,Ngang Peter,Ngoma Pauline,Omgba Vincent,Omam Deborah,Tonfack Léonie,Zé Flore,Akongnwi Emmanuel,Dumortier Jérôme,Ngoupo Paul-Alain,Njouom Richard,Rousset Dominique,Le Fouler Lenaig,Madec Yoann,Bodelet Marine,Dupre Jean-Michel,Pavie Juliette,Rekacewicz Claire,Garcia Paula,Colin Géraldine,

Affiliation:

1. Faculty of Medicine and Pharmaceutical Sciences, University of Dschang, Yaoundé Central Hospital, Cameroon

2. Normandy Université, Université de Rouen Normandie, Groupe de Recherche sur l’Adaptation Microbienne, EA Rouen University Hospital, Laboratory of Virology associated with the National Reference Centre for HIV

3. Unit of Epidemiology of Emerging Diseases, Institut Pasteur, Paris, France

4. Virology Department, Centre Pasteur of Cameroon, Yaoundé

5. Recherche Translationnelle sur le VIH et les Maladies Infectieuses, University of Montpellier, Institut de Recherche et pour le Développement, Institut National de la Santé et de la Recherche Médicale

6. Faculty of Medicine Paris Diderot, University Hospital Saint Louis, Paris, France

Abstract

AbstractBackgroundLittle is known about impact of genetic divergence of human immunodeficiency virus type 1 group O (HIV-1/O) relative to HIV-1 group M (HIV-1/M) on therapeutic outcomes. We aimed to determine if responses to standardized combination antiretroviral therapy (cART) were similar between groups despite strain divergence.MethodsWe performed an open nonrandomized study comparing the immunological, virological, and clinical responses to cART based on 2 nucleoside reverse transcriptase inhibitors plus 1 ritonavir-boosted protease inhibitor, in naive and paired HIV-1/O vs HIV-1/M infected (+) patients (ratio 1:2), matched on several criteria. The primary endpoint was the proportion of patients with undetectable plasma viral load (pVL, threshold 60 copies/mL) at week (W) 48. Secondary endpoints were the proportion of patients with undetectable pVL at W24 and W96 and CD4 evolution between baseline and W24, W48, and W96.ResultsForty-seven HIV-1/O+ and 94 HIV-1/M+ patients were included. Mean pVL at baseline was significantly lower by 1 log for HIV-1/O+ vs HIV-1/M+ patients. At W48, no significant difference was observed between populations with undetectable pVL and differences at W24 and W96 were not significant. A difference in CD4 gain was observed in favor of HIV-1/M at W48 and W96, but this was not significant when adjusted on both matched criteria and pVL at baseline.ConclusionsOur data demonstrate similar immunovirological and clinical response between HIV-1/O+ and HIV-1/M+ patients. They also reveal significantly lower baseline replication for HIV-1/O variants, suggesting specific virological properties and physiopathology that now need to be addressed.Clinical Trials RegistrationNCT00658346.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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