AN INHIBITOR OF THE PROTEASE BLOCKS MATURATION OF HUMAN AND SIMIAN IMMUNODEFICIENCY VIRUSES AND SPREAD OF INFECTION

被引:210
作者
ASHORN, P
MCQUADE, TJ
THAISRIVONGS, S
TOMASSELLI, AG
TARPLEY, WG
MOSS, B
机构
[1] UPJOHN LABS,KALAMAZOO,MI 49001
[2] NIAID,VIRAL DIS LAB,BETHESDA,MD 20892
关键词
acquired immunodeficiency syndrome; anti-viral therapy; peptidomimetic inhibitor;
D O I
10.1073/pnas.87.19.7472
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The activity of the human immunodeficiency virus (HIV) protease is essential for processing of the gag-pol precursor proteins and maturation of infectious virions. We have prepared a peptidomimetic inhibitor, U-75875, that inhibited HIV-1 gag-pol protein processing in an essentially irreversible manner. Noninfectious virus particles produced in the presence of the drug contained gag precursors and were morphologically immature. In human peripheral blood mono-nuclear cells and in a continuous cell line, U-75875 completely blocked HIV replication; in the latter case, no spread occurred over a period of 4 weeks. U-75875, on a molar basis, was as potent as 3'-azido-3'-deoxythymidine in blocking HIV-1 replication in human lymphocytes and also inhibited HIV-2 and simian immunodeficiency virus proteases, demonstrating that it has broad activity. These results provide further evidence for the therapeutic potential of protease inhibitors in HIV infection.
引用
收藏
页码:7472 / 7476
页数:5
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