Expression of Tissue Factor by Eosinophils in Patients with Chronic Urticaria

被引:101
作者
Cugno, Massimo [1 ]
Marzano, Angelo V. [2 ]
Tedeschi, Alberto [3 ]
Fanoni, Daniele [2 ]
Venegoni, Luigia [2 ]
Asero, Riccardo [4 ]
机构
[1] IRCCS Fdn Maggiore Policlin Hosp, Dept Internal Med, Milan, Italy
[2] IRCCS Fdn Maggiore Policlin Hosp, Inst Dermatol Sci, Milan, Italy
[3] IRCCS Fdn Maggiore Policlin Hosp, Allergy & Clin Immunol Unit, Milan, Italy
[4] Clin San Carlo, Milan, Italy
关键词
Tissue factor; Eosinophils; Chronic urticaria; Skin; AUTOLOGOUS SERUM; ANTI-IGE; AUTOANTIBODIES; ACTIVATION; PLASMA;
D O I
10.1159/000155748
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Although several cases of chronic urticaria (CU) are currently regarded as autoimmune in origin, associated with histamine-releasing autoantibodies, an activation of blood coagulation via tissue factor (TF) and a strong expression of TF in lesional skin have been described. Eosinophils, which are involved in CU skin lesions, have recently been demonstrated as the major source of TF in human blood. We assessed whether eosinophils are the cellular source of TF in CU skin lesions. Methods: Twenty patients with severe CU were studied. Skin biopsy specimens were taken from wheals. The control group consisted of specimens of perilesional normal skin from different types of skin tumours (10) and various skin disorders with non-eosinophilic infiltrates, including leukocytoclastic vasculitis (7), lichen planus (8) and mastocytosis (3). TF expression was evaluated by immunohistochemical methods using an anti-TF monoclonal antibody. Co-localization of TF and eosinophil cationic protein, a classic cell marker of eosinophils, was investigated by double-staining studies using 2 specific monoclonal antibodies in the 4 specimens showing the highest TF reactivity scores. Results: All specimens from patients with CU clearly showed TF expression that was absent in all normal control specimens (p = 0.0001) and in the skin disorders with non-eosinophilic infiltrates (p = 0.001-0.0001). The double-staining experiments for TF and eosinophil cationic protein clearly showed that the TF-positive cells were eosinophils. Conclusions: Eosinophils are the main source of TF in CU lesional skin. This finding highlights the role of these cells in the pathophysiology of CU and might pave the way for new therapeutic strategies. Copyright (C) 2008 S. Karger AG, Basel
引用
收藏
页码:170 / 174
页数:5
相关论文
共 19 条
[1]   Severe chronic urticaria is associated with elevated plasma levels of D-dimer [J].
Asero, R. ;
Tedeschi, A. ;
Riboldi, P. ;
Griffini, S. ;
Bonanni, E. ;
Cugno, M. .
ALLERGY, 2008, 63 (02) :176-180
[2]   Chronic urticaria: novel clinical and serological aspects [J].
Asero, R ;
Tedeschi, A ;
Lorini, M ;
Salimbeni, R ;
Zanoletti, T ;
Miadonna, A .
CLINICAL AND EXPERIMENTAL ALLERGY, 2001, 31 (07) :1105-1110
[3]   Plasma of patients with chronic urticaria shows signs of thrombin generation, and its intradermal injection causes wheal-and-flare reactions much more frequently than autologous serum [J].
Asero, R ;
Tedeschi, A ;
Riboldi, P ;
Cugno, M .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 117 (05) :1113-1117
[4]   Activation of the tissue factor pathway of blood coagulation in patients with chronic urticaria [J].
Asero, Riccardo ;
Tedeschi, Alberto ;
Coppola, Raffaella ;
Griffini, Samantha ;
Paparella, Paolo ;
Riboldi, Piersandro ;
Marzano, Angelo V. ;
Fanoni, Daniele ;
Cugno, Massimo .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2007, 119 (03) :705-710
[5]   Monocytes, but not macrophages, produce the eosinophil cationic protein [J].
Byström, J ;
Tenno, T ;
Håkansson, L ;
Amin, K ;
Trulson, A ;
Högbom, E ;
Venge, P .
APMIS, 2001, 109 (7-8) :507-516
[6]   Thrombin functions as an inflammatory mediator through activation of its receptor [J].
Cirino, G ;
Cicala, C ;
Bucci, MR ;
Sorrentino, L ;
Maraganore, JM ;
Stone, SR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (03) :821-827
[7]  
Fagiolo U, 2000, J ALLERGY CLIN IMMUN, V106, P567, DOI 10.1067/mai.2000.108913
[8]   DETECTION OF CIRCULATING HISTAMINE RELEASING AUTOANTIBODIES WITH FUNCTIONAL-PROPERTIES OF ANTI-IGE IN CHRONIC URTICARIA [J].
GRATTAN, CEH ;
FRANCIS, DM ;
HIDE, M ;
GREAVES, MW .
CLINICAL AND EXPERIMENTAL ALLERGY, 1991, 21 (06) :695-704
[9]   AUTOANTIBODIES AGAINST THE HIGH-AFFINITY IGE RECEPTOR AS A CAUSE OF HISTAMINE-RELEASE IN CHRONIC URTICARIA [J].
HIDE, M ;
FRANCIS, DM ;
GRATTAN, CEH ;
HAKIMI, J ;
KOCHAN, JP ;
GREAVES, MW .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (22) :1599-1604
[10]   Late-phase urticaria update [J].
Kambe N. ;
Kitao A. ;
Nishigori C. ;
Miyachi Y. .
Current Allergy and Asthma Reports, 2002, 2 (4) :288-291