Eotaxin and eosinophil recruitment: implications for human disease

被引:198
作者
Rankin, SM [1 ]
Conroy, DM [1 ]
Williams, TJ [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Div Biomed Sci, Leukocyte Biol Sect, London SW7 2AZ, England
来源
MOLECULAR MEDICINE TODAY | 2000年 / 6卷 / 01期
关键词
D O I
10.1016/S1357-4310(99)01635-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eosinophils have been implicated in a broad range of diseases, notably allergic conditions (for example, asthma, rhinitis and atopic dermatitis) and other inflammatory disorders (for example, inflammatory bowel disease, eosinophilic gastroenteritis and pneumonia). These disease states are characterized by an accumulation of eosinophils in tissues. Severe tissue damage ensues as eosinophils release their highly cytotoxic granular proteins. Defining the mechanisms that control recruitment of eosinophils to tissues is fundamental to understanding these disease processes and provides targets for novel drug therapy. An important discovery in this context was the identification of an eosinophil-specific chemoattractant, eotaxin. Over the past six years there has been intensive investigation into the biological effects of eotaxin and its role in specific disease processes and this is the subject of this review.
引用
收藏
页码:20 / 27
页数:8
相关论文
共 61 条
[1]   Human chemokines: An update [J].
Baggiolini, M ;
Dewald, B ;
Moser, B .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :675-705
[2]   Human dermal fibroblasts express eotaxin: Molecular cloning, mRNA expression, and identification of eotaxin sequence variants [J].
Bartels, J ;
Schluter, C ;
Richter, E ;
Noso, N ;
Kulke, R ;
Christophers, E ;
Schroder, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 225 (03) :1045-1051
[3]  
Bartels Joachim, 1997, Rhinology (Utrecht), V35, P171
[4]  
BOCHNER BS, 1995, J IMMUNOL, V154, P799
[5]   Eotaxin stimulates eosinophil adhesion to human lung microvascular endothelial cells [J].
BurkeGaffney, A ;
Hellewell, PG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 227 (01) :35-40
[6]  
Campbell EM, 1998, J IMMUNOL, V161, P7047
[7]   The beta-chemokine receptors CCR3 and CCR5 facilitate infection by primary HIV-1 isolates [J].
Choe, H ;
Farzan, M ;
Sun, Y ;
Sullivan, N ;
Rollins, B ;
Ponath, PD ;
Wu, LJ ;
Mackay, CR ;
LaRosa, G ;
Newman, W ;
Gerard, N ;
Gerard, C ;
Sodroski, J .
CELL, 1996, 85 (07) :1135-1148
[8]   COOPERATION BETWEEN INTERLEUKIN-5 AND THE CHEMOKINE EOTAXIN TO INDUCE EOSINOPHIL ACCUMULATION IN-VIVO [J].
COLLINS, PD ;
MARLEAU, S ;
GRIFFITHSJOHNSON, DA ;
JOSE, PJ ;
WILLIAMS, TJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (04) :1169-1174
[9]   The role of the eosinophil-selective chemokine, eotaxin, in allergic and non-allergic airways inflammation [J].
Conroy, DM ;
Humbles, AA ;
Rankin, SM ;
Palframan, RT ;
Collins, PD ;
Griffiths-Johnson, DA ;
Jose, PJ ;
Williams, TJ .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 1997, 92 :183-191
[10]   Cloning, expression, and characterization of the human eosinophil eotaxin receptor [J].
Daugherty, BL ;
Siciliano, SJ ;
DeMartino, JA ;
Malkowitz, L ;
Sirotina, A ;
Springer, MS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) :2349-2354