HIV-1 integrase inhibitors: A decade of research and two drugs in clinical trial

被引:118
作者
Johnson, AA [1 ]
Marchand, C [1 ]
Pommier, Y [1 ]
机构
[1] NCI, Mol Pharmacol Lab, CCR, NIH, Bethesda, MD 20892 USA
关键词
HIV-1; integrase; diketo acids; HIV inhibitors; AIDS; integrase inhibitors;
D O I
10.2174/1568026043388394
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
AIDS is currently treated with a combination therapy of reverse transcriptase and protease inhibitors. Recently, the FDA approved a drug targeting HIV-1 entry into cells. There are currently no FDA approved drugs targeting HIV-1 integrase, though many scientists and drug companies are actively in pursuit of clinically useful integrase inhibitors. The objective of this review is to provide an update on integrase inhibitors reported in the last two years, including two novel inhibitors in early clinical trials, recently developed hydroxylated aromatics, natural products, peptide, antibody and oligonucleotide inhibitors. Additionally, the proposed mechanism of diketo acid inhibition is reviewed.
引用
收藏
页码:1059 / 1077
页数:19
相关论文
共 104 条
[1]   Isolation of two highly potent and non-toxic inhibitors of human immunodeficiency virus type 1 (HIV-1) integrase from Salvia miltiorrhiza [J].
Abd-Elazem, IS ;
Chen, HS ;
Bates, RB ;
Huang, RCC .
ANTIVIRAL RESEARCH, 2002, 55 (01) :91-106
[2]   A metal-induced conformational change and activation of HIV-1 integrase [J].
AsanteAppiah, E ;
Skalka, AM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (26) :16196-16205
[3]   MONOCLONAL-ANTIBODIES AGAINST HIV TYPE-1 INTEGRASE - CLUES TO MOLECULAR-STRUCTURE [J].
BIZUBBENDER, D ;
KULKOSKY, J ;
SKALKA, AM .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1994, 10 (09) :1105-1115
[4]   Inhibition of HIV-1 by an anti-integrase single-chain variable fragment (SFv): delivery by SV40 provides durable protection against HIV-1 and does not require selection [J].
BouHamdan, M ;
Duan, LX ;
Pomerantz, RJ ;
Strayer, DS .
GENE THERAPY, 1999, 6 (04) :660-666
[5]  
BouHamdan M, 2000, J HUMAN VIROL, V3, P6
[6]   Inhibition of HIV-1 infection by down-regulation of the CXCR4 co-receptor using an intracellular single chain variable fragment against CXCR4 [J].
BouHamdan, M ;
Strayer, DS ;
Wei, D ;
Mukhtar, M ;
Duan, LX ;
Hoxie, J ;
Pomerantz, RJ .
GENE THERAPY, 2001, 8 (05) :408-418
[7]   Disruption of HIV-1 integrase-DNA complexes by short 6-oxocytosine-containing oligonucleotides [J].
Brodin, P ;
Pinskaya, M ;
Buckle, M ;
Parsch, U ;
Romanova, E ;
Engels, J ;
Gottikh, M ;
Mouscadet, JF .
BIOCHEMISTRY, 2002, 41 (05) :1529-1538
[8]   6-Oxocytidine containing oligonucleotides inhibit the HIV-1 integrase in vitro [J].
Brodin, P ;
Pinskaya, M ;
Parsch, U ;
Bischerour, J ;
Leh, H ;
Romanova, E ;
Engels, JW ;
Gottikh, M ;
Mouscadet, JF .
NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, 2001, 20 (4-7) :481-486
[9]   Binding of different divalent cations to the active site of avian sarcoma virus integrase and their effects on enzymatic activity [J].
Bujacz, G ;
Alexandratos, J ;
Wlodawer, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (29) :18161-18168
[10]   INHIBITORY EFFECT OF THE POLYANIONIC DRUG SURAMIN ON THE IN-VITRO HIV DNA INTEGRATION REACTION [J].
CARTEAU, S ;
MOUSCADET, JF ;
GOULAOUIC, H ;
SUBRA, F ;
AUCLAIR, C .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 305 (02) :606-610