Increased plasma eotaxin in atopic dermatitis and acute urticaria in infants and children

被引:41
作者
Hossny, E
Aboul-Magd, M
Bakr, S
机构
[1] Ain Shams Univ, Dept Clin Pathol, Cairo, Egypt
[2] Ain Shams Univ, Dept Dermatol & Venerol, Cairo, Egypt
[3] Ain Shams Univ, Dept Pediat, Cairo, Egypt
关键词
angioedema; atopic dermatitis; chemokines; children; eosinophil; infants; plasma eotaxin; urticaria;
D O I
10.1034/j.1398-9995.2001.00169.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: The previously reported eotaxin overexpression in the lesional skin of atopic dermatitis (AD) led us to the assumption that circulating levels of eotaxin may be elevated too. We sought to investigate the plasma expression of eotaxin in children with skin allergy in relation to clinical activity and type of lesions. Methods: Plasma cotaxin was assayed in 78 infants and children, of whom 16 had AD, 19 had acute urticaria (AU), and 43 were healthy matched subjects. Seven children in the group of AU were resampled for plasma cotaxin after clinical remission. Results: The plasma eotaxin levels in AD (median = 158 pg/ml, mean [SD] = 168 [61] pg/ml) were significantly higher than the control values (median = 60 pg/ml, mean [SD]= 59.5 [18.5] pg/ml). Not only did patients with AU demonstrate elevated plasma eotaxin levels (median = 126 pg/ml, mean [SD] = 124 [33] pg/ml), but also a significant decline occurred on follow-up. The coexistence of angioedema with AU did not cause any further increase in plasma eotaxin expression. Plasma eotaxin levels were significantly higher in AD than in AU, probably reflecting the chronic nature of eczematous AD lesions. The plasma eotaxin levels did not correlate with serum total I-E, peripheral blood absolute eosinophil count, or age of the patients. However, there was a positive correlation between age and plasma eotaxin in the control group. Conclusions: Our findings imply that circulating levels of cotaxin increase in AD and during flares of AU, probably to serve in the recruitment and activation of eosinophils. It may also represent a biomarker of lesional activity.
引用
收藏
页码:996 / 1002
页数:7
相关论文
共 44 条
[1]  
[Anonymous], ACTA DERM VENERE S92, DOI [10.2340/00015555924447, DOI 10.2340/00015555924447]
[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]   Dermal eosinophils in atopic dermatitis undergo cytolytic degeneration [J].
Cheng, JF ;
Ott, NL ;
Peterson, EA ;
George, TJ ;
Hukee, MJ ;
Gleich, GJ ;
Leiferman, KM .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1997, 99 (05) :683-692
[4]  
DAUHERTY BL, 1996, J EXP MED, V183, P2349
[5]   Novel co-operation between eotaxin and substance-P in inducing eosinophil-derived neurotoxin release [J].
El-Shazly, A ;
Ishikawa, T .
MEDIATORS OF INFLAMMATION, 1999, 8 (03) :177-179
[6]  
FRANK MM, 2000, CECIL TXB MED, P1440
[7]   IL-4 induces eotaxin production in corneal keratocytes but not in epithelial cells [J].
Fukagawa, K ;
Nakajima, T ;
Saito, H ;
Tsubota, K ;
Shimmura, S ;
Natori, M ;
Hirai, K .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2000, 121 (02) :144-150
[8]   Human eotaxin is a specific chemoattractant for eosinophil cells and provides a new mechanism to explain tissue eosinophilia [J].
GarciaZepeda, EA ;
Rothenberg, ME ;
Ownbey, RT ;
Celestin, J ;
Leder, P ;
Luster, AD .
NATURE MEDICINE, 1996, 2 (04) :449-456
[9]  
GAY JC, 1999, WINTROBES CLIN HEMAT, P1836
[10]  
Geaghan S.M., 2000, HEMATOLOGY BASIC PRI, P2520