HIV-1 integrase: A target for new AIDS chemotherapeutics

被引:78
作者
Anthony, NJ [1 ]
机构
[1] Merck Res Labs, Dept Med Chem, West Point, PA 19486 USA
关键词
D O I
10.2174/1568026043388448
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Since the beginning of the HIV epidemic almost 70 million people have been infected with HIV. It is estimated that 42 million people are currently living with HIV/AIDS. The spread of HIV continues throughout the world and current estimates indicate that in 2002, 5 million people were newly infected with HIV and 3 million people died. Current treatments employ a combination of therapeutic agents that target the viral reverse transcriptase and protease enzymes and viral entry. However the clinical benefit of these agents is often limited due to issues of regimen compliance, significant side effects, and the emergence of viral strains that are drug resistant. The introduction of novel agents that interfere with alternate stages in the viral life cycle represent potential solutions to these problems. The integration of the HIV genome into the cellular chromosome, a process catalyzed by the viral enzyme integrase, has been shown to be essential for viral replication. Since HIV integrase has no direct cellular counterpart it presents itself as an attractive target for therapeutic intervention. This review summarizes recent and promising developments both in the HIV integrase field and the global quest for therapeutically useful inhibitors of HIV integrase.
引用
收藏
页码:979 / 990
页数:12
相关论文
共 76 条
[31]  
2-A
[32]   Potent suppression of HIV-1 replication in humans by T-20, a peptide inhibitor of gp41-mediated virus entry [J].
Kilby, JM ;
Hopkins, S ;
Venetta, TM ;
DiMassimo, B ;
Cloud, GA ;
Lee, JY ;
Alldredge, L ;
Hunter, E ;
Lambert, D ;
Bolognesi, D ;
Mathews, T ;
Johnson, MR ;
Nowak, MA ;
Shaw, GM ;
Saag, MS .
NATURE MEDICINE, 1998, 4 (11) :1302-1307
[33]   RESIDUES CRITICAL FOR RETROVIRAL INTEGRATIVE RECOMBINATION IN A REGION THAT IS HIGHLY CONSERVED AMONG RETROVIRAL RETROTRANSPOSON INTEGRASES AND BACTERIAL INSERTION-SEQUENCE TRANSPOSASES [J].
KULKOSKY, J ;
JONES, KS ;
KATZ, RA ;
MACK, JPG ;
SKALKA, AM .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (05) :2331-2338
[34]   A cellular cofactor in HIV-1 assembly: INI1 is also an 'outtie' [J].
Landau, NR .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2002, 23 (06) :252-253
[35]  
LEAVITT AD, 1993, J BIOL CHEM, V268, P2113
[36]   Approaches to the design of effective HIV-1 protease inhibitors [J].
Lebon, F ;
Ledecq, M .
CURRENT MEDICINAL CHEMISTRY, 2000, 7 (04) :455-477
[37]   A previously unidentified host protein protects retroviral DNA from autointegration [J].
Lee, MS ;
Craigie, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1528-1533
[38]  
LEESE P, 2002, 14 INT AIDS C BARC S
[39]   Highly active antiretroviral therapy in a large urban clinic: Risk factors for virologic failure and adverse drug reactions [J].
Lucas, GM ;
Chaisson, RE ;
Moore, RD .
ANNALS OF INTERNAL MEDICINE, 1999, 131 (02) :81-+
[40]   Structure-based mutational analysis of the C-terminal DNA-Binding domain of human immunodeficiency virus type 1 integrase: Critical residues for protein oligomerization and DNA binding [J].
Lutzke, RAP ;
Plasterk, RHA .
JOURNAL OF VIROLOGY, 1998, 72 (06) :4841-4848