Thalidomide and thalidomide analogs reduce HIV type 1 replication in human macrophages in vitro

被引:72
作者
Moreira, AL
Corral, LG
Ye, WG
Johnson, B
Stirling, D
Muller, GW
Freedman, VH
Kaplan, G
机构
[1] ROCKEFELLER UNIV,CELLULAR PHYSIOL & IMMUNOL LAB,NEW YORK,NY 10021
[2] CELGENE CORP,WARREN,NJ 07059
关键词
D O I
10.1089/aid.1997.13.857
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Thalidomide is currently being evaluated for efficacy in alleviating some manifestations of HIV-I infection, To determine whether thalidomide has any direct effects on HIV-1 infection, we investigated the effect of thalidomide and also of three structural analogs of thalidomide on HIV-1 replication in vitro in human monocyte-derived macrophages, The thalidomide analogs were previously shown to inhibit TNF-alpha production in vitro at much lower concentrations than thalidomide. In HIV-l-infected macrophages treated with thalidomide or thalidomide analogs, viral replication was reduced by 60 to 80% as determined by measuring viral RT activity in the culture supernatants. In all experiments the analogs inhibited HIV-1 replication more efficiently than did thalidomide, The drugs also reduced HIV-1 gag mRNA expression. Furthermore, the drugs caused a decrease in NF-kappa B-binding activity in nuclear extracts of HIV-l-infected macrophages. The role of NF-kappa B in the drug-induced inhibition of HIV-1 replication was confirmed using an NF-kappa B-defective mutant virus to infect macrophages.
引用
收藏
页码:857 / 863
页数:7
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