CCR5 inhibitors in HIV-1 therapy

被引:17
作者
Dorr, Patrick [1 ]
Perros, Manos [2 ]
机构
[1] Pfizer Ltd, Global R&D, Primary Pharmacol, Sandwich Labs, Sandwich CT13 9NJ, Kent, England
[2] Antiviral Res, Sandwich CT13 9NJ, Kent, England
关键词
antiretroviral; aplaviroc; ART; CCR5; HAART; HIV-1; INCB9471; maraviroc; PF-232798; resistance; SCH-532706; TAK-220; TAK-652; TAK-779; Trofile (TM); tropism; vicriviroc;
D O I
10.1517/17460441.3.11.1345
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The human immunodeficiency virus 1 (HIV-1) is the causative pathogen of AIDS, the world's biggest infectious disease killer. About 33 million people are infected worldwide, with 2.1 million deaths a year as a direct consequence. The devastating nature of AIDS has prompted widespread research, which has led to an extensive array of therapies to suppress viral replication and enable recovery of the immune system to prolong and improve patient life substantially. However, the genetic plasticity and replication rate of HIV-1 are considerable, which has lead to rapid drug resistance. This, together with the need for reducing drug side effects and increasing regimen compliance, has led researchers to identify antiretroviral drugs with new modes of action. Objective: This review describes the discovery and clinical development of CCR5 antagonists and the recent approval of maraviroc as a breakthrough in anti-HIV-1 therapy. Conclusion: CCR5 inhibitors target a human cofactor to disable HIV-1 entry into the cells, and thereby provide a new hurdle for the virus to overcome. The status and expert opinion of CCR5 antagonists for the treatment of HIV-1 infection are detailed.
引用
收藏
页码:1345 / 1361
页数:17
相关论文
共 144 条
[1]  
Anonymous, 2005, Antiviral Chemistry & Chemotherapy, V16, P339
[2]   The discovery of tropane-derived CCR5 receptor antagonists [J].
Armour, DR ;
de Groot, MJ ;
Price, DA ;
Stammen, BLC ;
Wood, A ;
Perros, M ;
Burt, C .
CHEMICAL BIOLOGY & DRUG DESIGN, 2006, 67 (04) :305-308
[3]  
AYOUB A, 14 C RETR OPP INF 20
[4]   TAK-652 inhibits CCR5-mediated human immunodeficiency virus type 1 infection in vitro and has favorable pharmacokinetics in humans [J].
Baba, M ;
Takashima, K ;
Miyake, H ;
Kanzaki, N ;
Teshima, K ;
Wang, X ;
Shiraishi, M ;
Iizawa, Y .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (11) :4584-4591
[5]   A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activity [J].
Baba, M ;
Nishimura, O ;
Kanzaki, N ;
Okamoto, M ;
Sawada, H ;
Iizawa, Y ;
Shiraishi, M ;
Aramaki, Y ;
Okonogi, K ;
Ogawa, Y ;
Meguro, K ;
Fujino, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (10) :5698-5703
[6]   ISOLATION OF A T-LYMPHOTROPIC RETROVIRUS FROM A PATIENT AT RISK FOR ACQUIRED IMMUNE-DEFICIENCY SYNDROME (AIDS) [J].
BARRESINOUSSI, F ;
CHERMANN, JC ;
REY, F ;
NUGEYRE, MT ;
CHAMARET, S ;
GRUEST, J ;
DAUGUET, C ;
AXLERBLIN, C ;
VEZINETBRUN, F ;
ROUZIOUX, C ;
ROZENBAUM, W ;
MONTAGNIER, L .
SCIENCE, 1983, 220 (4599) :868-871
[7]   The core domain of chemokines binds CCR5 extracellular domains while their amino terminus interacts with the transmembrane helix bundle [J].
Blanpain, C ;
Doranz, BJ ;
Bondue, A ;
Govaerts, C ;
De Leener, A ;
Vassart, G ;
Doms, RW ;
Proudfoot, A ;
Parmentier, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (07) :5179-5187
[8]   Cigarette smoke-induced pulmonary inflammation, but not airway remodelling, is attenuated in chemokine receptor 5-deficient mice [J].
Bracke, K. R. ;
D'hulst, A. I. ;
Maes, T. ;
Demedts, I. K. ;
Moerloose, K. B. ;
Kuziel, W. A. ;
Joos, G. F. ;
Brusselle, G. G. .
CLINICAL AND EXPERIMENTAL ALLERGY, 2007, 37 (10) :1467-1479
[9]  
Bredeek UF, 2007, EUR J MED RES, V12, P427
[10]  
Buchbinder Susan, 2008, Top HIV Med, V16, P9