The history of antiretrovirals: key discoveries over the past 25 years

被引:134
作者
De Clercq, Erik [1 ]
机构
[1] Katholieke Univ Leuven, Rega Inst Med Res, Lab Chemotherapy, Dept Microbiol & Immunol, B-3000 Louvain, Belgium
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; CHRONIC HEPATITIS-B; TRANSCRIPTASE INHIBITORS NNRTIS; ACYCLIC NUCLEOSIDE PHOSPHONATES; TREATMENT-EXPERIENCED PATIENTS; RESISTANT HIV-1 INFECTION; DEPENDENT DNA POLYMERASE; REVERSE-TRANSCRIPTASE; SELECTIVE-INHIBITION; ADEFOVIR DIPIVOXIL;
D O I
10.1002/rmv.624
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Within 25 years after zidovudine (3'-azido-2',3'-dideoxythymidine, AZT) was first described as an inhibitor of HIV replication, 25 anti-HIV drugs have been formally approved for clinical use in the treatment of HIV infections: seven nucleoside reverse transcriptase inhibitors (NRTIs): zidovudine, didanosine, zalcitabine, stavudine, lamivudine, abacavir and emtricitabine; one nucleotide reverse transcriptase inhibitor (NtRTI): tenofovir [in its oral prodrug form: tenofovir disoproxil fumarate (TDF)]; four non-nucleoside reverse transcriptase inhibitors (NNRTIs): nevirapine, delavirdine, efavirenz and etravirine; ten protease inhibitors (PIs): saquinavir, ritonavir, indinavir, nelfinavir, amprenavir, lopinavir, atazanavir, fosamprenavir, tipranavir and darunavir; one fusion inhibitor (FI): enfuvirtide; one co-receptor inhibitor (CRI): maraviroc and one integrase inhibitor (INI): raltegravir. These compounds are used in various drug combination (some at fixed dose) regimens so as to achieve the highest possible benefit and tolerability, and to diminish the risk of virus-drug resistance development. Copyright (C) 2009 John Wiley & Sons, Ltd.
引用
收藏
页码:287 / 299
页数:13
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