CD4 cell response to 3 doses of subcutaneous interleukin 2: Meta-analysis of 3 Vanguard studies

被引:26
作者
Arduino, RC
Nannini, EC
Rodriguez-Barradas, M
Schrader, S
Losso, M
Ruxrungtham, K
Allende, MC
Emery, S
Fosdick, L
Neaton, J
Tavel, JA
Davey, RT
Lane, HC
机构
[1] Univ Texas, Hlth Sci Ctr, Houston, TX 77030 USA
[2] Baylor Coll Med, Houston, TX 77030 USA
[3] Vet Affairs Med Ctr, Houston, TX 77030 USA
[4] Montrose Clin, Houston, TX USA
[5] NIAID, NIH, Bethesda, MD 20892 USA
[6] Univ Minnesota, Sch Publ Hlth, Div Biostat, Coordinating Ctr Biometr Res, Minneapolis, MN 55455 USA
[7] Hosp JM Ramos Mejia, Buenos Aires, DF, Argentina
[8] Chulalongkorn Univ, Dept Med, Bangkok, Thailand
[9] Thai Red Cross AIDS Res Ctr, HIVNAT, Bangkok, Thailand
[10] Univ New S Wales, Natl Ctr HIV Epidemiol & Clin Res, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1086/421775
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. In advance of a large clinical end point trial evaluating the effectiveness of subcutaneous interleukin 2 (scIL-2) for treatment of patients with human immunodeficiency virus (HIV) infection, 3 identically designed Vanguard trials were conducted in Buenos Aires, Argentina; Bangkok, Thailand; and Houston, Texas. To more precisely quantitate the effect on CD4 cell response of 3 different doses of scIL-2 that were administered twice daily for 5 days every 8 weeks, the results of these 3 trials were pooled in a meta-analysis. Methods. Two hundred eighteen HIV-1-infected subjects who were receiving antiretroviral therapy and who had a baseline CD4 cell count of greater than or equal to350 cells/mm(3) were consecutively randomized to receive scIL-2 at a dose of 1.5 mIU (n = 36) or a control regimen (n = 36); or scIL-2 at a dose of 4.5 mIU (n = 36) or a control regimen (n = 36); or scIL- 2 at a dose of 7.5 mIU (n = 37) or a control regimen (n = 36). After completion of 3 cycles of therapy, the subjects were enrolled in an extension phase (months 6-12). Subjects were encouraged to receive additional cycles of scIL-2 to maintain a CD4 cell count of more than twice the baseline count or >1000 cells/mm(3). Results. After completion of 3 cycles of scIL-2, the mean CD4 cell count changes from baseline (calculated as changes from baseline in a scIL-2 group minus changes from baseline in its contemporaneous control group) were 67 (P = .14), 339 (P < .0001), and 605 cells/mm(3) (P < .0001) for the 1.5, 4.5, and 7.5 mIU dose groups, respectively ( for differences among dose groups). Between months 6 and 12, a total of 78%, 39%, and 32% of subjects assigned to the 1.5, 4.5, and 7.5 mIU dose groups, respectively, needed at least 1 additional cycle to achieve the CD4 cell count goal. At 12 months, the differences in the mean change in CD4 cell count from baseline between each scIL-2 dose group and its contemporaneous control group were 184, 369, and 432 cells/mm(3), respectively (for differences among dose groups). Conclusions. Although CD4 cell count increases were seen in all 3 dose groups, higher scIL-2 doses resulted in greater CD4 cell count changes after 6 months, compared with control groups.
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页码:115 / 122
页数:8
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