HIV-1 Antiretroviral Drug Therapy

被引:543
作者
Arts, Eric J. [1 ]
Hazuda, Daria J. [2 ]
机构
[1] Case Western Reserve Univ, Dept Med, Div Infect Dis, Ugandan CFAR Labs, Cleveland, OH 44106 USA
[2] Merck Res Labs, West Point, PA 19486 USA
来源
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE | 2012年 / 2卷 / 04期
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; REVERSE-TRANSCRIPTASE INHIBITORS; ZIDOVUDINE RESISTANCE MUTATIONS; DEPENDENT PRIMER UNBLOCKING; CORECEPTOR-BINDING-SITE; HIGH-LEVEL RESISTANCE; IN-VIVO EMERGENCE; INTEGRASE INHIBITORS; SMALL-MOLECULE; PROTEASE INHIBITORS;
D O I
10.1101/cshperspect.a007161
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The most significant advance in the medical management of HIV-1 infection has been the treatment of patients with antiviral drugs, which can suppress HIV-1 replication to undetectable levels. The discovery of HIV-1 as the causative agent of AIDS together with an ever-increasing understanding of the virus replication cycle have been instrumental in this effort by providing researchers with the knowledge and tools required to prosecute drug discovery efforts focused on targeted inhibition with specific pharmacological agents. To date, an arsenal of 24 Food and Drug Administration (FDA)-approved drugs are available for treatment of HIV-1 infections. These drugs are distributed into six distinct classes based on their molecular mechanism and resistance profiles: (1) nucleoside-analog reverse transcriptase inhibitors (NNRTIs), (2) non-nucleoside reverse transcriptase inhibitors (NNRTIs), (3) integrase inhibitors, (4) protease inhibitors (PIs), (5) fusion inhibitors, and (6) coreceptor antagonists. In this article, we will review the basic principles of antiretroviral drug therapy, the mode of drug action, and the factors leading to treatment failure (i.e., drug resistance).
引用
收藏
页数:23
相关论文
共 167 条
[1]   Nature, Position, and Frequency of Mutations Made in a Single Cycle of HIV-1 Replication [J].
Abram, Michael E. ;
Ferris, Andrea L. ;
Shao, Wei ;
Alvord, W. Gregory ;
Hughes, Stephen H. .
JOURNAL OF VIROLOGY, 2010, 84 (19) :9864-9878
[2]   CC CKRS: A RANTES, MIP-1 alpha, MIP-1 beta receptor as a fusion cofactor for macrophage-tropic HIV-1 [J].
Alkhatib, G ;
Combadiere, C ;
Broder, CC ;
Feng, Y ;
Kennedy, PE ;
Murphy, PM ;
Berger, EA .
SCIENCE, 1996, 272 (5270) :1955-1958
[3]   Cross-resistance among nonnucleoside reverse transcriptase inhibitors limits recycling efavirenz after nevirapine failure [J].
Antinori, A ;
Zaccarelli, M ;
Cingolani, A ;
Forbici, F ;
Rizzo, MG ;
Trotta, MP ;
Di Giambenedetto, S ;
Narciso, P ;
Ammassari, A ;
Girardi, E ;
De Luca, A ;
Perno, CF .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 2002, 18 (12) :835-838
[4]  
Arion D, 1998, BIOCHEMISTRY-US, V37, P15908
[5]   Positive effects of combined antiretroviral therapy on CD4(+) T cell homeostasis and function in advanced HIV disease [J].
Autran, B ;
Carcelain, G ;
Li, TS ;
Blanc, C ;
Mathez, D ;
Tubiana, R ;
Katlama, C ;
Debre, P ;
Leibowitch, J .
SCIENCE, 1997, 277 (5322) :112-116
[6]   Isolation and characterization of human immunodeficiency virus type 1 resistant to the small-molecule CCR5 antagonist TAK-652 [J].
Baba, Masanori ;
Miyake, Hiroshi ;
Wang, Xin ;
Okamoto, Mika ;
Takashima, Katsunori .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (02) :707-715
[7]   Genotypic correlates of phenotypic resistance to efavirenz in virus isolates from patients failing nonnucleoside reverse transcriptase inhibitor therapy [J].
Bacheler, L ;
Jeffrey, S ;
Hanna, G ;
D'Aquila, R ;
Wallace, L ;
Logue, K ;
Cordova, B ;
Hertogs, K ;
Larder, B ;
Buckery, R ;
Baker, D ;
Gallagher, K ;
Scarnati, H ;
Tritch, R ;
Rizzo, C .
JOURNAL OF VIROLOGY, 2001, 75 (11) :4999-5008
[8]   Human immunodeficiency virus type 1 mutations selected in patients failing efavirenz combination therapy [J].
Bacheler, LT ;
Anton, ED ;
Kudish, P ;
Baker, D ;
Bunville, J ;
Krakowski, K ;
Bolling, L ;
Aujay, M ;
Wang, XV ;
Ellis, D ;
Becker, MF ;
Lasut, AL ;
George, HJ ;
Spalding, DR ;
Hollis, G ;
Abremski, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (09) :2475-2484
[9]   Emergence of a drug-dependent human immunodeficiency virus type 1 variant during therapy with the T20 fusion inhibitor [J].
Baldwin, CE ;
Sanders, RW ;
Deng, YQ ;
Jurriaans, S ;
Lange, JM ;
Lu, M ;
Berkhout, B .
JOURNAL OF VIROLOGY, 2004, 78 (22) :12428-12437
[10]  
BALZARINI J, 1989, J BIOL CHEM, V264, P6127