In vivo antagonism with zidovudine plus stavudine combination therapy

被引:65
作者
Havlir, DV
Tierney, C
Friedland, GH
Pollard, RB
Smeaton, L
Sommadossi, JP
Fox, L
Kessler, H
Fife, KH
Richman, DD
机构
[1] Univ Calif San Diego, San Diego, CA 92103 USA
[2] San Diego VA Med Ctr, San Diego, CA USA
[3] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[4] Yale Univ, Sch Med, New Haven, CT 06510 USA
[5] Univ Texas, Galveston, TX 77555 USA
[6] Univ Alabama, Birmingham, AL 35294 USA
[7] NIH, Div AIDS, Bethesda, MD 20892 USA
[8] Rush Presbyterian St Lukes Med Ctr, Chicago, IL 60612 USA
[9] Indiana Univ, Med Ctr, Indianapolis, IN 46204 USA
关键词
D O I
10.1086/315683
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human immunodeficiency virus (HIV)-infected subjects receiving zidovudine were randomized either to add stavudine (d4T) or didanosine (ddI) to their current regimen or to switch to ddI or d4T monotherapy, After 16 weeks of therapy, the mean reduction in HIV RNA from baseline was 0.14 log(10) copies/mL in patients receiving d4T or zidovudine plus d4T. In subjects receiving ddI or ddI plus zidovudine, reductions were 0.39 and 0.56 log(10), respectively. CD4 cell counts remained stable or showed modest increases in all arms except the zidovudine plus d4T arm. Patients receiving zidovudine plus d4T showed progressive declines in CD4 cell counts with a median of 22 cells/mm(3) below baseline by 16 weeks. Examination of intracellular levels of d4T-triphosphate in 6 subjects was consistent with previous in vitro studies demonstrating pharmacologic antagonism between zidovudine and d4T. Analysis of these data suggests that zidovudine and d4T should not be prescribed in combination and that ddI provides greater antiviral activity than d4T in zidovudine-treated patients.
引用
收藏
页码:321 / 325
页数:5
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