Clinical, immunological and virological response to different antiretroviral regimens in a cohort of HIV-2-infected patients

Marchina E van der Ende, Jan M Prins, Kees Brinkman, Monique Keuter, Jan Veenstra, Sven A Danner, Hubert G M Niesters, Albert D M E Osterhaus, Martin Schutten

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

OBJECTIVE: To assess the clinical, immunological and virological response and the emergence of resistance towards antiretroviral therapy (ART) in a cohort of HIV-2-infected patients.

DESIGN: Observational study.

PATIENTS: HIV-2-infected patients residing in the Netherlands.

RESULTS: From 1995 to 2001 seven patients failed various ART regimens. The resistance mutations were analysed retrospectively. Development of mutations proved to be similar to that observed in HIV-1-infected patients, with the exception of a higher occurrence of the Q151M mutation within the reverse transcriptase gene. In a prospective study, comprising 13 consecutive naive HIV-2-infected patients, all patients achieved plasma HIV-2-RNA suppression below the detection limit (500 copies/ml). The antiretroviral regimen consisted of two nucleoside reverse transcriptase inhibitors (NRTIs) and indinavir, with a boosting dose of ritonavir; the median follow-up was 91 weeks. Two patients experienced a temporary virological rebound, while at the same time therapeutic drug monitoring showed sub-therapeutic plasma levels of indinavir.

CONCLUSION: Sustained viral suppression in HIV-2-infected patients can be achieved using an antiretroviral regimen of two NRTIs and boosted indinavir or lopinavir.

Original languageEnglish
Pages (from-to)S55-61
Number of pages7
JournalAids
Volume17 Suppl 3
Publication statusPublished - Jul-2003
Externally publishedYes

Keywords

  • Adult
  • Aged
  • Anti-HIV Agents
  • CD4 Lymphocyte Count
  • Drug Resistance, Viral
  • Drug Therapy, Combination
  • Female
  • Genes, Viral
  • Genotype
  • HIV Infections
  • HIV Protease Inhibitors
  • HIV-2
  • Humans
  • Male
  • Middle Aged
  • Mutation
  • Prospective Studies
  • Retrospective Studies
  • Reverse Transcriptase Inhibitors
  • Salvage Therapy
  • Treatment Failure
  • Viral Load

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