3-DRUG SYNERGISTIC INHIBITION OF HIV-1 REPLICATION INVITRO BY ZIDOVUDINE, RECOMBINANT SOLUBLE CD4, AND RECOMBINANT INTERFERON-ALPHA-A

被引:74
作者
JOHNSON, VA
BARLOW, MA
MERRILL, DP
CHOU, TC
HIRSCH, MS
机构
[1] HARVARD UNIV,SCH MED,BOSTON,MA 02115
[2] MEM SLOAN KETTERING CANC CTR,PHARMACOL LAB,NEW YORK,NY 10021
关键词
D O I
10.1093/infdis/161.6.1059
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Optimal management of human immunodeficiency virus type 1 (HIV-l) infections may require combinations of agents that attack different targets in the viral replicative cycle. Zidovudine (AZT), recombinant soluble CD4 (rsCD4), and recombinant interferon-alpha A (rIFN-αA) were evaluated in 2- and 3-drug regimens against HIV-l replication in vitro. Peripheral blood mononuclear cells and a CD4+T cell line (H9) were studied using multiple HIV-l replicative end points. Drug interactions were evaluated by the median-effect principle and the isobologram technique. AZT, rsCD4, and rIFN-αA inhibited HIV-l synergistically in 2- and 3-drug combinations. The 3-drug regimen provided more complete virus suppression than the 2-drug regimens. In H9 cells, single-drug regimens lost effectiveness at 10-14 days and 2-drug regimens lost effectiveness at 14-18 days. In contrast, the 3-drug regimen showed nearly complete suppression over 28 days in culture without toxicity. Clinical trials of these 3 drugs in combination should be considered. © 1990, University of Chicago. All rights reserved.
引用
收藏
页码:1059 / 1067
页数:9
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