HIV-1 Subtypes and Response to Combination Antiretroviral Therapy in Europe

Author:

,Bannister Wendy P1,Ruiz Lidia2,Loveday Clive3,Vella Stefano4,Zilmer Kai5,Kjær Jesper6,Knysz Brygida7,Phillips Andrew N1,Mocroft Amanda1,Lundgren Jens D6

Affiliation:

1. Department of Primary Care and Population Sciences, Royal Free and University College Medical School, London, UK

2. Hospital Universitari Germans Trias i Pujol, Badalona, Spain

3. ICVC-International Clinical Virology Centre, Buckinghamshire, UK

4. Instituto Superiore di Sanita, Rome, Italy

5. West-Tallinn Central Hospital, Tallinn, Estonia

6. Copenhagen HIV Programme, Hvidovre Hospital, Copenhagen, Denmark

7. Medical University, Wroclaw, Poland

Abstract

Background Combination antiretroviral therapy (cART) may vary in ability to suppress viral load and increase CD4+ T-cell count in people infected with different HIV-1 subtypes, possibly due to differences in resistance development. Antiretroviral drugs have predominantly been developed in Western Europe/North America on the basis of the most prevalent subtype, B. However, non-B subtypes are increasingly spreading worldwide. Objective To compare virological and immunological response to cART between patients infected with B and non-B subtypes across Europe. Design EuroSIDA prospective, observational cohort with 11,928 HIV-1-infected patients. Methods Response to cART was analysed in patients with subtypes determined pre-cART, via multivariable logistic regression on the first measurements 6–12 months after starting cART. A virological response was defined as a viral load <500 copies/ml and immunological response as a CD4+ T-cell count increase of ≥100 cells/mm3. Results Forty-five percent of patients were antiretroviral naive at initiation of cART. Virological suppression was achieved by 58% of 689 subtype-B-infected patients and 66% of 102 non-B-infected patients ( P=0.159). After adjustment for potential confounders, there was no significant difference in odds of achieving virological suppression (non-B compared with B; odds ratio [OR]: 1.05, 95% confidence interval [CI]: 0.58–1.93, P=0.866). An immunological response was achieved by 43% of 753 B-infected patients and 48% of 114 non-B-infected patients ( P=0.334). After adjustment, there was no significant difference in odds of an immunological response (OR: 1.17, 95% CI: 0.73–1.87, P=0.524). Conclusions There was no evidence of significant differences in virological or immunological response to cART between patients infected with HIV-1 B and non-B subtypes.

Publisher

SAGE Publications

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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