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
[41]   Highly potent HIV inhibition:: engineering a key anti-HIV structure from PSC-RANTES into MIP-1β/CCL4 [J].
Gaertner, Hubert ;
Lebeau, Olivier ;
Borlat, Irene ;
Cerini, Fabrice ;
Dufour, Brigitte ;
Kuenzi, Gabriel ;
Melotti, Astrid ;
Fish, Richard J. ;
Offord, Robin ;
Springael, Jean-Yves ;
Parmentier, Marc ;
Hartley, Oliver .
PROTEIN ENGINEERING DESIGN & SELECTION, 2008, 21 (02) :65-72
[42]   ISOLATION OF HUMAN T-CELL LEUKEMIA-VIRUS IN ACQUIRED IMMUNE-DEFICIENCY SYNDROME (AIDS) [J].
GALLO, RC ;
SARIN, PS ;
GELMANN, EP ;
ROBERTGUROFF, M ;
RICHARDSON, E ;
KALYANARAMAN, VS ;
MANN, D ;
SIDHU, GD ;
STAHL, RE ;
ZOLLAPAZNER, S ;
LEIBOWITCH, J ;
POPOVIC, M .
SCIENCE, 1983, 220 (4599) :865-867
[43]   The CCR5-D32 mutation: impact on disease outcome in individuals with hepatitis C infection from a single source [J].
Goulding, C ;
Murphy, A ;
MacDonald, G ;
Barrett, S ;
Crowe, J ;
Hegarty, J ;
McKiernan, S ;
Kelleher, D .
GUT, 2005, 54 (08) :1157-1161
[44]  
GREAVES W, 2006, 13 C RETR OPP INF
[45]   Resistance to enfuvirtide, the first HIV fusion inhibitor [J].
Greenberg, ML ;
Cammack, N .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 54 (02) :333-340
[46]  
HEERA J, 15 C RETR OPP INF 20
[47]   CC-type chemokine receptor 5-Δ32 mutation protects against primary sclerosing cholangitis [J].
Henckaerts, L ;
Fevery, J ;
Van Steenbergen, W ;
Werslype, C ;
Yap, P ;
Nevens, F ;
Roskams, T ;
Libbrecht, L ;
Rutgeerts, P ;
Vermeire, S .
INFLAMMATORY BOWEL DISEASES, 2006, 12 (04) :272-277
[48]   Safety, pharmacokinetics, and antiviral activity of AMD3100, a selective CXCR4 receptor inhibitor, in HIV-1 infection [J].
Hendrix, CW ;
Collier, AC ;
Lederman, MM ;
Schols, D ;
Pollard, RB ;
Brown, S ;
Jackson, JB ;
Coombs, RW ;
Gleshy, MJ ;
Flexner, CW ;
Bridger, GJ ;
Badel, K ;
MacFarland, RT ;
Henson, GW ;
Calandra, G .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2004, 37 (02) :1253-1262
[49]  
HOEPELMAN I, 2007, 11 EUR AIDS C EACS
[50]  
Hoffmann C, 2007, EUR J MED RES, V12, P385