New approaches to morphological diagnosis of gluten-sensitive celiac disease


如何引用文章

全文:

详细

Aim. To characterize cell adhesion molecules (CAM), components of intercellular matrix (ICM) in gluten-sensitive celiac disease (GSCD).
Material and methods. A histological examination was made of biopsies of small intestinal mucosa (SIM) obtained from 890 patients with clinical and laboratory symptoms of GSCD. Of them, 124(14%) patients had signs of chronic atrophic duodenitis of different severity corresponding to GSCD. Newly diagnosed GSCD was in 63(7.1%) patients, 61 (6,9 %) patients kept aglutenic diet. Biopsy specimens from unaffected mucosa of distal parts of the duodenum from 10 patients served control. Immunohistochemical examination of CAM and ICM was made using antibodies to E-cadgerin, beta-catenin, CD44, type IV collagen, matrix metalloproteinase of type 9 (MMP-9).
Results. Interrupted weak reaction in epithelial basal membrane and enhanced expression of this antigen in stroma were observed in SIM in GSCD of stage IIIC by Marsh. Subnormal irregular expression of E-cadgerin and beta-catenin were seen in membrane of surface epithelium and cryptal epithelium. Moreover, high CD44 expression was detected in membrane of SIM stroma cells and high expression of MMP-9 in the cytoplasm of stromal cells and intercellular matrix.
Conclusion. The detected disorders of intercellular and cellular-matrix interaction in GSCD promote tissue lesion, increased permeability of epithelial barrier and changes in histogenesis processes. Further study of minimal disorders in SIM in GSCD on the molecular level will facilitate diagnosis of early stages of the disease and prognosis of its course.

作者简介

Natal'ya Vorob'eva

Email: VorobyevaN@yandex.ru

Sergey Khomeriki

Asfol'd Parfenov

N Vorobyeva

Central Research Institute of Gastroenterology, Moscow

Central Research Institute of Gastroenterology, Moscow

S Khomeriki

Central Research Institute of Gastroenterology, Moscow

Central Research Institute of Gastroenterology, Moscow

A Parfenov

Central Research Institute of Gastroenterology, Moscow

Central Research Institute of Gastroenterology, Moscow

参考

  1. Louglin R., Sebastian S. S., Qasim A. et al. Celiac disease in Europe. Aliment. Pharmacol. Ther. 2003; 18 (Suppl. 3): 45-48.
  2. Парфенов А. И. Целиакия. Эволюция представлений о распространенности, клинических проявлениях и значимости этиотропной терапии. М.: Анахарсис; 2007.
  3. Leffler D. A., Dennis M., Hyett B. et al. Etiologies and predictors of diagnosis in nonresponsive celiac disease. Clin. Gastroenterol. Hepatol. 2007; 5 (4): 445-450.
  4. Rostom A., Murray J. A., Kagnoff M. A. American Gastroenterological Association (AGA) Institute. Technical review on the diagnosis and management of celiac disease. Gastroenterology 2006; 131: 1981-2002.
  5. Аруин Л. И., Каппулер Л. Л., Исаков В. А. Морфологическая диагностика болезней желудка и кишечника. М.: Триада-Х; 1998.
  6. Bonamico M., Mariani P., Thanasi E. et al. Duodenal atrophy or proximal duodenal involvement by coeliac disease? J. Pediatr. Gastroenterol. Nutr. 2004; 39 (2): 217-218.
  7. Ravelli A., Bolognini S., Gambarotti M., Villanacci V. Variability of histologic lesions in relation to biopsy site in glutensensitive enteropathy. Am. J. Gastroenterol. 2005; 100 (1): 177-185.
  8. Marsh M. N., Crowe P. T. Morphology of the mucosal lesion in gluten sensitivity. Bailliere's Clin. Gastroenterol. 1995; 9: 273-293.
  9. Oberhuber G., Granditsch G., Vogelsang H. The histopathology of coeliac disease: time for a standardized report scheme for pathologists. Eur. J. Gastroenterol. Hepatol. 1999; 11 (10): 1185-1194.
  10. Corazza G. R., Villanacci V. Coeliac disease. Some considerations on the histological classification. J. Clin. Pathol. 2005; 58: 573-574.
  11. Лысиков Ю. А. Нерешенные и не решаемые вопросы целиакии. Клиническое питание 2006; 1-2: 49-52.
  12. Hayat M., Cairns A., Dixon M. F., O'Mahony S. Quantitation of intraepithelial lymphocytes in human duodenum: what is normal? J. Clin. Pathol. 2002; 55 (5): 393-394.
  13. Jarvinen T. T., Kaukinen K., Laurila K. et al. Intraepithelial lymphocytes in coeliac disease. Am. J. Gastroenterol. 2003; 98 (6): 1332-1337.
  14. Brown I., Mino-Kenudson M., Deshpande V., Lawers G. Y. Intraepithelial lymphocytosis in architecturally preserved proximal small intestinal mucosa: an increasing diagnostic problem with a wide differential diagnosis. Arch. Pathol. Lab. Med. 2006; 130: 1020-1025.
  15. Бельмер С. В., Гасилина Т. В., Усачева А. Ю. Современные концепции патогенеза целиакии. Экспер. и клин. гастроэнтерол. 2010; 1: 86-92.
  16. Sander G. R., Cummins A. G., Henshall T. et al. Rapid disruption of intestinal barrier function by gliadin involves altered expression of apical functional proteins. FEBS Lett. 2005; 579 (21): 4851-4855.
  17. Drago S., El Asmar R., Di Pierro M. Gliadin, zonulin and gut permeability: Effects on celiac and non-celiac intestinal mucosa and intestinal cell lines. Scand. J. Gastroenterol. 2006; 41 (4): 408-419.
  18. Zebrowska A., Narbutt J., Sysa-Jedrzejowska A. et al. The imbalance between metalloproteinases and their tissue inhibitors is involved in the pathogenesis of dermatitis herpetiformis. Мediators Inflamm. 2005; 6: 373-379.
  19. Mohamed B. M., Feighery C., Kelly J. Increased protein expression of matrix metalloproteinases -1, -3, and -9 and TIMP-1 in patients with gluten-sensitive enteropathy. Dig. Dis. Sci. 2006; 51 (10): 1862-1868.

补充文件

附件文件
动作
1. JATS XML

版权所有 © Consilium Medicum, 2012

Creative Commons License
此作品已接受知识共享署名-非商业性使用-相同方式共享 4.0国际许可协议的许可。
 

Address of the Editorial Office:

  • Alabyan Street, 13/1, Moscow, 127055, Russian Federation

Correspondence address:

  • Alabyan Street, 13/1, Moscow, 127055, Russian Federation

Managing Editor:

  • Tel.: +7 (926) 905-41-26
  • E-mail: e.gorbacheva@ter-arkhiv.ru

 

© 2018-2021 "Consilium Medicum" Publishing house


##common.cookie##