Altered expression of IgG and complement receptors indicates a significant role of phagocytes in atopic dermatitis

被引:24
作者
Isolauri, E
Pelto, L
Nuutila, J
Majamaa, H
Lilius, EM
Salminen, S
机构
[1] UNIV TURKU,DEPT BIOCHEM & FOOD CHEM,FIN-20520 TURKU,FINLAND
[2] UNIV TAMPERE,DEPT PAEDIAT,FIN-33101 TAMPERE,FINLAND
基金
芬兰科学院;
关键词
complement receptors; atopic dermatitis; Fc receptors; food allergy; hypersensitivity;
D O I
10.1016/S0091-6749(97)70034-4
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Strict dietary precautions against allergic sensitization may benefit a group of predisposed children. Objective, To develop new strategies for identifying these children, a better understanding of the processes that initiate sensitization and regulate and perpetuate the inflammatory response is needed, Methods: We measured the expression of the receptors for the constant (Fc) region of IgG (Fc gamma RI, Fc gamma RII, and Fc gamma RIII) and that for the complement fragments C3b and C3bi (CRI and CR3) in neutrophils and monocytes from 39 children with atopic dermatitis, 17 disease control patients with acute infections, and 17 healthy control subjects. The capacity of phagocytes to produce reactive oxygen species was also determined, To find the best way of discriminating the patients with atopic dermatitis from control subjects, a stepwise logistic binary regression model was made, Results: The stepwise logistic regression analysis was based on differences in individual receptor expression between the study groups, Because acute infections strongly affected receptor expression in both neutrophils and monocytes, to avoid diagnostic bias, children with acute infections were excluded from the analysis, The combination of the receptors CR1 in neutrophils and Fc gamma R1 and Fc gamma RII in monocytes was the best indicator of atopic dermatitis. A significant correlation between the expression of CRI in neutrophils and in monocytes, as well as reactive oxygen species production of phagocytes, and the severity of the eczema was detected, Conclusions: These results suggest that a distinct receptor profile of phagocytic cells can be characterized in patients with atopic dermatitis, providing a new direction to the search for early identification of children predisposed to allergic sensitization.
引用
收藏
页码:707 / 713
页数:7
相关论文
共 30 条
[1]   KERATINOCYTES AS INITIATORS OF INFLAMMATION [J].
BARKER, JNWN ;
MITRA, RS ;
GRIFFITHS, CEM ;
DIXIT, VM ;
NICKOLOFF, BJ .
LANCET, 1991, 337 (8735) :211-214
[2]   SURFACE EXPRESSION OF GP165/95, THE COMPLEMENT RECEPTOR CR3, AS A MARKER OF DISEASE-ACTIVITY IN SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
BUYON, JP ;
SHADICK, N ;
BERKMAN, R ;
HOPKINS, P ;
DALTON, J ;
WEISSMANN, G ;
WINCHESTER, R ;
ABRAMSON, SB .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1988, 46 (01) :141-149
[3]   AN ABNORMALITY OF THE GENE THAT ENCODES NEUTROPHIL FC-RECEPTOR-III IN A PATIENT WITH SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
CLARK, MR ;
LIU, L ;
CLARKSON, SB ;
ORY, PA ;
GOLDSTEIN, IM .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (01) :341-346
[4]   MOLECULAR-BASIS OF IGG FC RECEPTOR-III DEFECT IN A PATIENT WITH SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
ENENKEL, B ;
JUNG, D ;
FREY, J .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1991, 21 (03) :659-663
[5]  
*EUR TASK FORC AT, 1993, DERMATOLOGY, V186, P23
[6]   BOOSTED SYSTEMIC IMMUNE AND LOCAL RESPONSIVENESS AFTER INTESTINAL INFLAMMATION IN ORALLY SENSITIZED GUINEA-PIGS [J].
FARGEAS, MJ ;
THEODOROU, V ;
MORE, J ;
WAL, JM ;
FIORAMONTI, J ;
BUENO, L .
GASTROENTEROLOGY, 1995, 109 (01) :53-62
[7]  
FYFE A, 1987, CLIN EXP IMMUNOL, V67, P300
[8]   PHENOTYPIC ANALYSIS OF FUNCTIONALLY ASSOCIATED MOLECULES ON PERIPHERAL-BLOOD AND SYNOVIAL-FLUID MONOCYTES FROM ARTHRITIS PATIENTS [J].
GADD, SJ ;
FELZMANN, T ;
MAJDIC, O ;
MAURER, D ;
PETERA, P ;
CHEN, WJ ;
SMOLEN, J ;
KNAPP, W .
RHEUMATOLOGY INTERNATIONAL, 1992, 12 (04) :153-157
[9]   GRANULOCYTE ACTIVATION-INDUCED BY INTENSE INTERVAL RUNNING [J].
GRAY, AB ;
TELFORD, RD ;
COLLINS, M ;
BAKER, MS ;
WEIDEMANN, MJ .
JOURNAL OF LEUKOCYTE BIOLOGY, 1993, 53 (05) :591-597
[10]  
HANIFIN JM, 1987, MONOGR ALLERGY, V21, P116