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The Body Covers: The 6th Conference on Retroviruses and Opportunistic Infections
Abstract No. 357: A Randomized Controlled Multicenter Phase II Trial of Subcutaneous Interleukin-2 (scIL-2) Therapy in HIV-Infected Patients with CD4 Counts 200-500 cells/µL

February 2, 1999


This article is part of TheBody.com's archive. Because it contains information that may no longer be accurate, this article should only be considered a historical document.

This study, conducted by Davey and colleagues, was a randomized trial comparing treatment with subcutaneous (injected under the skin) interleukin-2 (IL-2) plus stable antiretroviral therapy (ARV) versus ARV therapy alone in 82 patients with baseline T-cell counts of 200-500 cells. The mean T-cell count was about 345, and the mean viral load was 3.1 log using the bDNA test. Thirty-nine patients were on the IL-2 arm, and 43 were on antiretroviral therapy alone. IL-2 recipients received 5-day courses every 8 weeks for 6 cycles at a starting dose of 7.5 MIU twice-a-day, decreased as needed for toxicity. Protease inhibitor use was between 80-90% on each arm. Results were as follows:


IL-2 plus ARV Baseline One Year
Mean CD4 Count (% increase): 355 739 (112% increase)
% pts., bDNA<500 copies/ml: 59% 68%
% pts., bDNA<50 copies/ml: 40% 67%

ARV alone Baseline One Year
Mean CD4 Count (% increase): 341 405 (18% increase)
% pts., bDNA<500 copies/ml: 44% 46%
% pts., bDNA<50 copies/ml: 31% 36%


The study investigators concluded that combination antiretroviral treatment with intermittent therapy with IL-2 led to a greater increase in CD4 cells, and a trend towards lower viral loads, than combination antiretroviral therapy alone.


This article is part of TheBody.com's archive. Because it contains information that may no longer be accurate, this article should only be considered a historical document.

Abstract: A Randomized Controlled Multicenter Phase II Trial of Subcutaneous Interleukin-2 (scIL-2) Therapy in HIV-Infected Patients with CD4 Counts 200-500 cells/µL
Authored by: R. Davey, R. Murphy, F. Graziano, S. Boswell, A. Pavia, M. Cancio, J. Nadler, D. Sahner, A-M. Duliege, W. Capra, C. Lane, and J. Kahn

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