Maraviroc: The first of a new class of antiretroviral agents

被引:153
作者
MacArthur, Rodger D. [1 ]
Novak, Richard M. [2 ]
机构
[1] Wayne State Univ, Detroit, MI 48201 USA
[2] Univ Illinois, Chicago, IL USA
关键词
D O I
10.1086/589289
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Maraviroc is the first US Food and Drug Administration-approved drug from a new class of antiretroviral agents that targets a host protein, the chemokine receptor CCR5, rather than a viral target. Binding of maraviroc to this cell-surface protein results in blocking human immunodeficiency virus type 1 (HIV-1) attachment to the coreceptor and prevents the virus from entering CD4(+) cells. In this review, we include the details of the discoveries that led to the development of this drug. The drug's pharmacology, including pharmacokinetics and drug interactions, is discussed, as are the clinical efficacy studies that led to licensure. HIV-1 mechanisms of resistance to maraviroc, assays to determine viral coreceptor use (tropism), drug safety, and clinical use of maraviroc are discussed at length.
引用
收藏
页码:236 / 241
页数:6
相关论文
共 37 条
[1]   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
[2]   THE CD4 (T4) ANTIGEN IS AN ESSENTIAL COMPONENT OF THE RECEPTOR FOR THE AIDS RETROVIRUS [J].
DALGLEISH, AG ;
BEVERLEY, PCL ;
CLAPHAM, PR ;
CRAWFORD, DH ;
GREAVES, MF ;
WEISS, RA .
NATURE, 1984, 312 (5996) :763-767
[3]   Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity [J].
Dorr, P ;
Westby, M ;
Dobbs, S ;
Griffin, P ;
Irvine, B ;
Macartney, M ;
Mori, J ;
Rickett, G ;
Smith-Burchnell, C ;
Napier, C ;
Webster, R ;
Armour, D ;
Price, D ;
Stammen, B ;
Wood, A ;
Perros, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (11) :4721-4732
[4]  
DUMOND J, 2008, 15 C RETR OPP INF BO
[5]   Efficacy of short-term monotherapy with maraviroc, a new CCR5 antagonist, in patients infected with HIV-1 [J].
Fätkenheuer, G ;
Pozniak, AL ;
Johnson, MA ;
Plettenberg, A ;
Staszewski, S ;
Hoepelman, AIM ;
Saag, MS ;
Goebel, FD ;
Rockstroh, JK ;
Dezube, BJ ;
Jenkins, TM ;
Medhurst, C ;
Sullivan, JF ;
Ridgway, C ;
Abel, S ;
James, IT ;
Youle, M ;
van der Ryst, E .
NATURE MEDICINE, 2005, 11 (11) :1170-1172
[6]   Evaluation of eight different bioinformatics tools to predict viral tropism in different human immunodeficiency virus type 1 subtypes [J].
Garrido, Carolina ;
Roulet, Vanessa ;
Chueca, Natalia ;
Poveda, Eva ;
Aguilera, Antonio ;
Skrabal, Katharina ;
Zahonero, Natalia ;
Carlos, Silvia ;
Garcia, Federico ;
Louis Faudon, Jean ;
Soriano, Vincent ;
de Mendoza, Carmen .
JOURNAL OF CLINICAL MICROBIOLOGY, 2008, 46 (03) :887-891
[7]   Chemokine receptor CCR5 promotes leukocyte trafficking to the brain and survival in West Nile virus infection [J].
Glass, WG ;
Lim, JK ;
Cholera, R ;
Pletnev, AG ;
Gao, JL ;
Murphy, PM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (08) :1087-1098
[8]  
GOETZ M, 2007, 4 INT AIDS SOC C SYD
[9]  
GOODRICH JM, 2007, 2007 ANN M INF DIS S
[10]  
Hardy D, 2008, 15 C RETR OPP INF BO