Similar IL-5, IL-3, and GM-CSF syntheses by eosinophils in the jejunal mucosa of patients with celiac disease and dermatitis herpetiformis

被引:27
作者
Desreumaux, P [1 ]
Delaporte, E
Colombel, JF
Capron, M
Cortot, A
Janin, A
机构
[1] CHU Lille, Lab Rech Malad Inflammat Intestinales, Lille, France
[2] Inst Pasteur, Ctr Immunol & Biol Parasitaire, INSERM, Unite U167, Lille, France
[3] CHRU, Hop Claude Huriez, Lille, France
[4] Hop St Louis, Lab Rech Univ Pathol, Inst Hematol, Ctr HAYEM, Paris, France
来源
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY | 1998年 / 88卷 / 01期
关键词
celiac disease; dermatitis herpetiformis; T-cells; eosinophils; cytokines;
D O I
10.1006/clin.1997.4494
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Celiac disease (CD) and dermatitis herpetiformis (DH) are gluten-sensitive diseases with different clinical features that can initiate similar intestinal changes. The flat-destructive stage corresponds to severe lesions involving activated T-cells. However, other inflammatory cells such as eosinophils are also abundant. The mechanisms for the intestinal recruitment of eosinophils in patients with CD and DH remain unknown. Eosinophil recruitment and activation are induced in vitro by three main cytokines: interleukin-3 (IL-3), interleukin-5 (IL-5), and granulocyte-macrophage colony-stimulating factor (GM-CSF), In this study, IL-3, IL-5, and GM-CSF were detected by immunohistochemistry in an patients with CD and DH but not in the control group. By ultrastructural immunogold staining, these three cytokines had the same subcellular localization in the granule matrix of eosinophils, This result suggests that eosinophils may be involved in the immune response at the fiat-destructive stage of both CD and DH. (C) 1998 Academic Press.
引用
收藏
页码:14 / 21
页数:8
相关论文
共 42 条
[1]  
ABUGHAZALEH RI, 1989, J IMMUNOL, V142, P2393
[2]   MAJOR HISTOCOMPATIBILITY COMPLEX SUSCEPTIBILITY GENES FOR DERMATITIS-HERPETIFORMIS COMPARED WITH THOSE FOR GLUTEN-SENSITIVE ENTEROPATHY [J].
AHMED, AR ;
YUNIS, JJ ;
MARCUSBAGLEY, D ;
YUNIS, EJ ;
SALAZAR, M ;
KATZ, AJ ;
AWDEH, Z ;
ALPER, CA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (06) :2067-2075
[3]   EOSINOPHILS EXPRESS INTERLEUKIN-5 AND GRANULOCYTE MACROPHAGE-COLONY-STIMULATING FACTOR MESSENGER-RNA AT SITES OF ALLERGIC INFLAMMATION IN ASTHMATICS [J].
BROIDE, DH ;
PAINE, MM ;
FIRESTEIN, GS .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (04) :1414-1424
[4]  
CLUTTERBUCK EJ, 1989, BLOOD, V73, P1504
[5]   COOPERATION BETWEEN INTERLEUKIN-5 AND THE CHEMOKINE EOTAXIN TO INDUCE EOSINOPHIL ACCUMULATION IN-VIVO [J].
COLLINS, PD ;
MARLEAU, S ;
GRIFFITHSJOHNSON, DA ;
JOSE, PJ ;
WILLIAMS, TJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (04) :1169-1174
[6]   ACTIVATED EOSINOPHILS IN ADULT CELIAC-DISEASE - EVIDENCE FOR A LOCAL RELEASE OF MAJOR BASIC-PROTEIN [J].
COLOMBEL, JF ;
TORPIER, G ;
JANIN, A ;
KLEIN, O ;
CORTOT, A ;
CAPRON, M .
GUT, 1992, 33 (09) :1190-1194
[7]   EOSINOPHILIA IN TRANSGENIC MICE EXPRESSING INTERLEUKIN-5 [J].
DENT, LA ;
STRATH, M ;
MELLOR, AL ;
SANDERSON, CJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (05) :1425-1431
[8]   Distinct cytokine patterns in early and chronic ileal lesions of Crohn's disease [J].
Desreumaux, P ;
Brandt, E ;
Gambiez, L ;
Emilie, D ;
Geboes, K ;
Klein, O ;
Ectors, N ;
Cortot, A ;
Capron, M ;
Colombel, JF .
GASTROENTEROLOGY, 1997, 113 (01) :118-126
[9]   Eosinophils in allergic reactions [J].
Desreumaux, P ;
Capron, M .
CURRENT OPINION IN IMMUNOLOGY, 1996, 8 (06) :790-795
[10]   INTERLEUKIN-5 MESSENGER-RNA EXPRESSION BY EOSINOPHILS IN THE INTESTINAL-MUCOSA OF PATIENTS WITH CELIAC-DISEASE [J].
DESREUMAUX, P ;
JANIN, A ;
COLOMBEL, JF ;
PRIN, L ;
PLUMAS, J ;
EMILIE, D ;
TORPIER, G ;
CAPRON, A ;
CAPRON, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (01) :293-296