Novel uses for anti-platelet agents as anti-inflammatory drugs

被引:55
作者
Pitchford, S. C. [1 ]
机构
[1] Imperial Coll, Natl Heart & Lung Inst, Leukocyte Biol Sect, London SW7 2AZ, England
关键词
platelets; inflammation; P2Y(1); P2Y(12); p-selectin; GPIIb/IIIa; CD40; S1P; PPAR;
D O I
10.1038/sj.bjp.0707364
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
An alteration in the character and function of platelets is manifested in patients with inflammatory diseases, and these alterations have been dissociated from the well-characterized involvement of platelets in thrombosis and haemostasis. Recent evidence reveals platelet activation is sometimes critical in the development of inflammation. The mechanisms by which platelets participate in inflammation are diverse, and offer numerous opportunities for future drug intervention. There is now acceptance that platelets act as innate inflammatory cells in immune responses, with roles as sentinel cells undergoing surveillance, responding to microbial invasion, orchestrating leukocyte recruitment, and migrating through tissue, causing damage and influencing repair processes in chronic disease. Some of these processes are targeted by drugs that are being developed to target platelet participation in atherosclerosis. The actions of platelets therefore influence the pathogenesis of diverse inflammatory diseases in various body compartments, encompassing parasitic and bacterial infection, allergic inflammation (especially asthma and rhinitis), and non-atopic inflammatory conditions, for example, chronic obstructive pulmonary disease (COPD), rheumatoid arthritis (RA), inflammatory bowel disease (IBD) and atherosclerosis. This review will first discuss the evidence for platelet activation in these various inflammatory diseases, and secondly discuss the mechanisms by which this pathogenesis occurs and the various anti-platelet agents which have been developed to combat platelet activation in atherosclerosis and their potential future use for the treatment of other inflammatory diseases.
引用
收藏
页码:987 / 1002
页数:16
相关论文
共 218 条
[51]   Enhanced thromboxane biosynthesis in patients with chronic obstructive pulmonary disease [J].
Davi, G ;
Basili, S ;
Vieri, M ;
Cipollone, F ;
Santarone, S ;
Alessandri, C ;
Gazzaniga, P ;
Cordova, C ;
Violi, F ;
DeLuca, N ;
Coppotelli, L ;
Paradiso, M ;
Bellomo, A ;
Belogi, A ;
Ferroni, P ;
Pulcinelli, F ;
Roccaforte, S ;
Antidormi, T .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 156 (06) :1794-1799
[52]   Modulation of airway hyperresponsiveness and eosinophilia by selective histamine and 5-HT receptor antagonists in a mouse model of allergic asthma [J].
De Bie, JJ ;
Henricks, PAJ ;
Cruikshank, WW ;
Hofman, G ;
Jonker, EH ;
Nijkamp, FP ;
Van Oosterhout, AJM .
BRITISH JOURNAL OF PHARMACOLOGY, 1998, 124 (05) :857-864
[53]   INHIBITION OF HUMAN EOSINOPHIL CHEMOTAXIS AND OF THE IGE-DEPENDENT STIMULATION OF HUMAN-BLOOD PLATELETS BY CETIRIZINE [J].
DEVOS, C ;
JOSEPH, M ;
LEPREVOST, C ;
VORNG, H ;
TOMASSINI, M ;
CAPRON, M ;
CAPRON, A .
INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1989, 88 (1-2) :212-215
[54]  
Diacovo TG, 1996, BLOOD, V88, P146
[55]   Platelet-mediated lymphocyte delivery to high endothelial venules [J].
Diacovo, TG ;
Puri, KD ;
Warnock, RA ;
Springer, TA ;
vonAndrian, UH .
SCIENCE, 1996, 273 (5272) :252-255
[56]   A FUNCTIONAL INTEGRIN LIGAND ON THE SURFACE OF PLATELETS - INTERCELLULAR-ADHESION MOLECULE-2 [J].
DIACOVO, TG ;
DEFOUGEROLLES, AR ;
BAINTON, DF ;
SPRINGER, TA .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (03) :1243-1251
[57]  
Dorn GW, 1997, AGENT ACTION SUPPL, V48, P42
[58]   Platelet-mediated modulation of adaptive immunity: A communication link between innate and adaptive immune compartments [J].
Elzey, BD ;
Tian, J ;
Jensen, RJ ;
Swanson, KA ;
Lees, JR ;
Lentz, SR ;
Stein, CS ;
Nieswandt, B ;
Wang, YQ ;
Davidson, BL ;
Ratliff, TL .
IMMUNITY, 2003, 19 (01) :9-19
[59]  
ENDRESEN GKM, 1992, CLIN EXP RHEUMATOL, V10, P181
[60]   EVIDENCE FOR ACTIVATION OF PLATELETS IN THE SYNOVIAL-FLUID FROM PATIENTS WITH RHEUMATOID-ARTHRITIS [J].
ENDRESEN, GKM .
RHEUMATOLOGY INTERNATIONAL, 1989, 9 (01) :19-24