Gluten-sensitive disease with mild enteropathy

被引:101
作者
Picarelli, A
Maiuri, L
Mazzilli, MC
Coletta, S
Ferrante, P
DiGiovambattista, F
Greco, M
Torsoli, A
Auricchio, S
机构
[1] UNIV NAPLES FEDERICO II,DEPT PEDIAT,I-80131 NAPLES,ITALY
[2] CHILDRENS HOSP PAUSILIPON,NAPLES,ITALY
[3] UNIV ROMA LA SAPIENZA,CATTEDRA GASTROENTEROL 1,ROME,ITALY
[4] UNIV ROMA LA SAPIENZA,MED CLIN 2,ROME,ITALY
[5] UNIV ROMA LA SAPIENZA,DEPT EXPT MED,I-00185 ROME,ITALY
关键词
D O I
10.1053/gast.1996.v111.pm8780564
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Celiac disease is a permanent gluten intolerance strongly associated with HLA class II antigens and possibly showing milder changes of mucosal architecture, Ten patients with symptoms suggesting celiac disease and serum antiendomysium antibodies with normal mucosal architecture were studied. Methods: Immunohistochemical detection of mucosal immune activation and HLA typings were performed. Results, Mucosal immune activation, with normal mucosal architecture and normal gamma/delta(+) intraepithelial lymphocytes counts, was found on a gluten-containing diet. In 3 of 6 patients, multiple biopsy specimens showed one sample with severe villous atrophy, Clinical and immunomorphologic features were strictly gluten dependent. The mucosal immune activation was elicited in vitro by gliadin, Only 4 patients had the typical HLA typing of celiac disease. Conclusions: Gluten-sensitive celiac-like symptoms may occur in patients with serum antiendomysium antibodies, apparently normal intestinal mucosa, and HL4 typing not commonly associated with celiac disease, These patients should undergo multiple biopsies, and signs of immunologic activation should be sought accurately; in the presence of mucosal immune activation, a trial with a gluten-free diet should be encouraged to detect gluten dependency, In vitro immunologic response of small intestinal mucosa to gliadin may support the diagnosis of gluten-sensitive enteropathy.
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收藏
页码:608 / 616
页数:9
相关论文
共 27 条
[1]  
AMAUDBATTENDIER F, 1986, GASTROENTEROLOGY, V91, P1206
[2]   INTESTINAL ANTIBODY PATTERN OF CELIAC-DISEASE - OCCURRENCE IN PATIENTS WITH NORMAL JEJUNAL BIOPSY HISTOLOGY [J].
ARRANZ, E ;
FERGUSON, A .
GASTROENTEROLOGY, 1993, 104 (05) :1263-1272
[3]   BETA-2-MICROGLOBULIN LEVELS IN CELIAC-DISEASE [J].
BONAMICO, M ;
CULASSO, F ;
PITZALIS, G ;
MARIANI, P ;
MORELLINI, M ;
PROCOPIO, A ;
TRIGLIONE, P ;
SIGNORETTI, A ;
BALLATI, G .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1990, 11 (03) :330-336
[4]  
BRANDTZAEG P, 1993, IMMUNOPHYSIOLOGY GUT, V11, P295
[5]   FOLLOW-UP OF PATIENTS POSITIVE IN RETICULIN AND GLIADIN ANTIBODY TESTS WITH NORMAL SMALL-BOWEL BIOPSY FINDINGS [J].
COLLIN, P ;
HELIN, H ;
MAKI, M ;
HALLSTROM, O ;
KARVONEN, AL .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1993, 28 (07) :595-598
[6]   A GENE DOSAGE EFFECT OF THE DQA1-ASTERISK-0501/DQB1-ASTERISK-0201 ALLELIC COMBINATION INFLUENCES THE CLINICAL HETEROGENEITY OF CELIAC-DISEASE [J].
CONGIA, M ;
CUCCA, F ;
FRAU, F ;
LAMPIS, R ;
MELIS, L ;
CLEMENTE, MG ;
CAO, A ;
DEVIRGILIIS, S .
HUMAN IMMUNOLOGY, 1994, 40 (02) :138-142
[7]  
COOPER BT, 1980, GASTROENTEROLOGY, V79, P801
[8]   GLIADIN INDUCED CHANGES IN THE EXPRESSION OF MHC-CLASS-II ANTIGENS BY HUMAN SMALL INTESTINAL EPITHELIUM - ORGAN-CULTURE STUDIES WITH CELIAC-DISEASE MUCOSA [J].
FAIS, S ;
MAIURI, L ;
PALLONE, F ;
DEVINCENZI, M ;
DERITIS, G ;
TRONCONE, R ;
AURICCHIO, S .
GUT, 1992, 33 (04) :472-475
[9]   CLINICAL AND PATHOLOGICAL SPECTRUM OF CELIAC-DISEASE ACTIVE, SILENT, LATENT, POTENTIAL [J].
FERGUSON, A ;
ARRANZ, E ;
OMAHONY, S .
GUT, 1993, 34 (02) :150-151
[10]   INTRAEPITHELIAL GAMMA-DELTA-T-CELL-RECEPTOR LYMPHOCYTES AND GENETIC SUSCEPTIBILITY TO CELIAC-DISEASE [J].
HOLM, K ;
MAKI, M ;
SAVILAHTI, E ;
LIPSANEN, V ;
LAIPPALA, P ;
KOSKIMIES, S .
LANCET, 1992, 339 (8808) :1500-1503