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Effects of intermittent IL-2 alone or with peri-cycle antiretroviral therapy in early HIV infection: the STALWART study

INSIGHT STALWART Study Group, Jens D. Lundgren (Member of author group)

16 Citations (Scopus)

Abstract

BACKGROUND: The Study of Aldesleukin with and without antiretroviral therapy (STALWART) evaluated whether intermittent interleukin-2 (IL-2) alone or with antiretroviral therapy (ART) around IL-2 cycles increased CD4(+) counts compared to no therapy.

METHODOLOGY: Participants not on continuous ART with > or = 300 CD4(+) cells/mm(3) were randomized to: no treatment; IL-2 for 5 consecutive days every 8 weeks for 3 cycles; or the same IL-2 regimen with 10 days of ART administered around each IL-2 cycle. CD4(+) counts, HIV RNA, and HIV progression events were collected monthly.

PRINCIPAL FINDINGS: A total of 267 participants were randomized. At week 32, the mean CD4(+) count was 134 cells greater in the IL-2 alone group (p<0.001), and 133 cells greater in the IL-2 plus ART group (p<0.001) compared to the no therapy group. Twelve participants in the IL-2 groups compared to 1 participant in the group assigned to no therapy experienced an opportunistic event or died (HR 5.84, CI: 0.59 to 43.57; p = 0.009).

CONCLUSIONS: IL-2 alone or with peri-cycle HAART increases CD4(+) counts but was associated with a greater number of opportunistic events or deaths compared to no therapy. These results call into question the immunoprotective significance of IL-2-induced CD4(+) cells.

TRIAL REGISTRATION: ClinicalTrials.gov NCT00110812.

Original languageEnglish
JournalPLoS One
Volume5
Issue number2
Pages (from-to)e9334
ISSN1932-6203
DOIs
Publication statusPublished - 23 Feb 2010
Externally publishedYes

Keywords

  • Adult
  • Anti-HIV Agents/adverse effects
  • Atazanavir Sulfate
  • CD4 Lymphocyte Count
  • Carbamates/therapeutic use
  • Drug Administration Schedule
  • Drug Therapy, Combination
  • Female
  • Fever/chemically induced
  • Furans
  • HIV Infections/drug therapy
  • Humans
  • Interleukin-2/adverse effects
  • Lopinavir
  • Male
  • Nausea/chemically induced
  • Oligopeptides/therapeutic use
  • Opportunistic Infections/chemically induced
  • Organophosphates/therapeutic use
  • Pyridines/therapeutic use
  • Pyrimidinones/therapeutic use
  • Ritonavir/therapeutic use
  • Sulfonamides/therapeutic use
  • Treatment Outcome

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