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 language | English |
|---|---|
| Journal | PLoS One |
| Volume | 5 |
| Issue number | 2 |
| Pages (from-to) | e9334 |
| ISSN | 1932-6203 |
| DOIs | |
| Publication status | Published - 23 Feb 2010 |
| Externally published | Yes |
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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