趋化因子受体
CCR1
CCR10
生物
趋化因子
CCL7型
CCL21型
趋化因子受体
趋化因子受体
CCL13型
细胞生物学
受体
免疫学
血管生成
CX3CL1型
癌症研究
炎症
遗传学
作者
Dévora L. Rossi,Albert Zlotnik
出处
期刊:Annual Review of Immunology
[Annual Reviews]
日期:2000-04-01
卷期号:18 (1): 217-242
被引量:2407
标识
DOI:10.1146/annurev.immunol.18.1.217
摘要
During the last five years, the development of bioinformatics and EST databases has been primarily responsible for the identification of many new chemokines and chemokine receptors. The chemokine field has also received considerable attention since chemokine receptors were found to act as co-receptors for HIV infection ( 1 ). In addition, chemokines, along with adhesion molecules, are crucial during inflammatory responses for a timely recruitment of specific leukocyte subpopulations to sites of tissue damage. However, chemokines and their receptors are also important in dendritic cell maturation ( 2 ), B ( 3 ), and T ( 4 ) cell development, Th1 and Th2 responses, infections, angiogenesis, and tumor growth as well as metastasis ( 5 ). Furthermore, an increase in the number of chemokine/receptor transgenic and knock-out mice has helped to define the functions of chemokines in vivo. In this review we discuss some of the chemokines’ biological effects in vivo and in vitro, described in the last few years, and the implications of these findings when considering chemokine receptors as therapeutic targets.
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