Dual targeting of CCR2 and CCR5: therapeutic potential for immunologic and cardiovascular diseases

被引:92
作者
Zhao, Qihong [1 ]
机构
[1] Bristol Myers Squibb Co, Res & Dev, Princeton, NJ 08543 USA
关键词
chemokines; chemokine receptors; disease pathogenesis; monocyte/macrophage recruitment; MONOCYTE CHEMOATTRACTANT PROTEIN-1; COLLAGEN-INDUCED ARTHRITIS; CHEMOKINE RECEPTOR CCR5; E-KNOCKOUT MICE; NILE-VIRUS-INFECTION; SMOOTH-MUSCLE-CELLS; ATHEROSCLEROTIC LESION DEVELOPMENT; CHANGES NEOINTIMAL HYPERPLASIA; SULFATE-MEDIATED COLITIS; IN-STENT RESTENOSIS;
D O I
10.1189/jlb.1009671
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A cardinal feature of inflammation is the tissue recruitment of leukocytes, a process that is mediated predominantly by chemokines via their receptors on migrating cells. CCR2 and CCR5, two CC chemokine receptors, are important players in the trafficking of monocytes/macrophages and in the functions of other cell types relevant to disease pathogenesis. This review provides a brief overview of the biological actions of CCR2 and CCR5 and a comprehensive summary of published data that demonstrate the involvement of both receptors in the pathogenesis of immunologic diseases (RA, CD, and transplant rejection) and cardiovascular diseases (atherosclerosis and AIH). In light of the potential for functional redundancy of chemokine receptors in mediating leukocyte trafficking and the consequent concern over insufficient efficacy offered by pharmacologically inhibiting one receptor, this review presents evidence supporting dual targeting of CCR2 and CCR5 as a more efficacious strategy than targeting either receptor alone. It also examines potential safety issues associated with such dual targeting. J. Leukoc. Biol. 88: 41-55; 2010.
引用
收藏
页码:41 / 55
页数:15
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