The relationship between serum levels of total IgE, IL-18, IL-12, IFN-γ and disease severity in children with atopic dermatitis

被引:42
作者
Aral, Murat [1 ]
Arican, Ozer
Gul, Mustafa
Sasmaz, Sezai
Kocturk, Sumeyra Alkis
Kastal, Ummugulsum
Ekerbicer, Hasan Cetin
机构
[1] Kahramanmaras Sutcu Imam Univ, Fac Med, Dept Microbiol & Clim Microbiol, TR-46100 Kahramanmaras, Turkey
[2] Kahramanmaras Sutcu Imam Univ, Fac Med, Dept Dermatol, TR-46100 Kahramanmaras, Turkey
[3] Kahramanmaras Sutcu Imam Univ, Fac Med, Dept Publ Hlth, TR-46100 Kahramanmaras, Turkey
关键词
D O I
10.1155/MI/2006/73098
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Studies about the role of cytokines on the immunopathogenesis of atopic dermatitis (AD) are generally based on in vitro observations and this role has not been completely clarified yet. Serum levels of total IgE, IL-18, IL-12, IFN-gamma and the relationship between these parameters and disease severity, determined using the SCORAD index, in a group of atopic patients were investigated in this study. Serum levels of total IgE were measured by the nephelometric method and serum levels of IL-18, IL-12/p40 and IFN-gamma were measured by ELISA method. Serum levels of total IgE and IL-18 were found significantly higher in study group than in controls (P < .001). There was no statistically significant difference between patients and controls in respect of serum levels of IL12/p40 (P = .227). A statistically significant relationship between SCORAD values and serum levels of total IgE (P < .001), IL-18 (P < .001), and IL-12/p40 (P < .001) was determined. These results show that serum levels of IL-18 can be a sensitive parameter that importantly correlates with clinical severity of AD, can play a role in the immunopathogenesis of AD, and furthermore may be used in the diagnosis and follow-up of the disease in addition to other parameters. Copyright (c) 2006 Murat Aral et al.
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页数:4
相关论文
共 32 条
[1]
DEMIS BJ, 1992, CLIN DERMATOL, P13
[2]
Serum concentration of IL-18 correlates with disease extent in young children with atopic dermatitis [J].
Ellis, KL ;
Leung, TF ;
Ma, KC ;
Wong, CK ;
Wan, H ;
Lam, CWK .
PEDIATRIC DERMATOLOGY, 2004, 21 (06) :619-622
[3]
CYTOKINE PRODUCTION BY MAST-CELLS AND BASOPHILS [J].
GALLI, SJ ;
GORDON, JR ;
WERSHIL, BK .
CURRENT OPINION IN IMMUNOLOGY, 1991, 3 (06) :865-873
[4]
ESTABLISHMENT OF A CELL-LINE WITH FEATURES OF EARLY DENDRITIC CELL PRECURSORS FROM FETAL MOUSE SKIN [J].
GIROLOMONI, G ;
LUTZ, MB ;
PASTORE, S ;
ABMANN, CU ;
CAVANI, A ;
RICCIARDICASTAGNOLI, P .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (08) :2163-2169
[5]
ATOPIC-DERMATITIS - IS IT AN ALLERGIC DISEASE [J].
HALBERT, AR ;
WESTON, WL ;
MORELLI, JG .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1995, 33 (06) :1008-1018
[6]
DIFFERENTIAL IN-SITU CYTOKINE GENE-EXPRESSION IN ACUTE VERSUS CHRONIC ATONIC DERMATITIS [J].
HAMID, Q ;
BOGUNIEWICZ, M ;
LEUNG, DYM .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (02) :870-876
[7]
ATOPIC-DERMATITIS [J].
HANIFIN, JM .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1984, 73 (02) :211-222
[8]
HANIFIN JM, 1980, ACTA DERM-VENEREOL, P44
[9]
Hoshino T, 1999, J IMMUNOL, V162, P5070
[10]
Hoshino T, 2000, EUR J IMMUNOL, V30, P1998, DOI 10.1002/1521-4141(200007)30:7<1998::AID-IMMU1998>3.0.CO