Oral proteases: a new approach to managing coeliac disease

被引:30
作者
Cerf-Bensussan, Nadine [1 ]
Matysiak-Budnik, Tamara [1 ]
Cellier, Christophe [1 ]
Heyman, Martine [1 ]
机构
[1] Fac Med Rene Descartes, INSERM U793, F-75730 Paris 15, France
关键词
PROLYL-ENDOPEPTIDASE; GLIADIN PEPTIDES; ENZYME THERAPY; GLUTEN; ASSOCIATION; EP-B2; CELLS;
D O I
10.1136/gut.2005.090498
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
A life-long but constraining gluten-free diet is the only treatment currently available for coeliac disease. The human gastrointestinal tract does not possess the enzymatic equipment to efficiently cleave the gluten-derived proline-rich peptides driving the abnormal immune intestinal response in patients with coeliac disease. Oral therapy by exogenous prolylendopeptidases able to digest ingested gluten was therefore propounded as an alternative treatment to the diet. The feasibility of this approach is discussed by reviewing recent data on the intestinal transport of gliadin peptides, properties of available enzymes and preliminary clinical assays. Development of new enzymes or enzymatic cocktails offers potentially more potent therapeutic tools that, however, need meticulous evaluation based on clinical, biological and histological criteria.
引用
收藏
页码:157 / 160
页数:4
相关论文
共 23 条
[1]   Heterologous expression, purification, refolding, and structural-functional characterization of EP-B2, a self-activating barley cysteine endoprotease [J].
Bethune, Michael T. ;
Strop, Pavel ;
Tang, Yinyan ;
Sollid, Ludvig M. ;
Khosla, Chaitan .
CHEMISTRY & BIOLOGY, 2006, 13 (06) :637-647
[2]   BREAKDOWN OF GLIADIN PEPTIDES BY INTESTINAL BRUSH-BORDERS FROM CELIAC PATIENTS [J].
BRUCE, G ;
WOODLEY, JF ;
SWAN, CHJ .
GUT, 1984, 25 (09) :919-924
[3]   Study of two ectopeptidases in the susceptibility to celiac disease: Two newly identified polymorphisms of dipeptidylpeptidase IV [J].
Clot, F ;
Babron, MC ;
Percopo, S ;
Giordano, M ;
Bouguerra, F ;
Clerget-Darpoux, F ;
Greco, L ;
Serre, JL ;
Fulchignoni-Lataud, MC .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2000, 30 (04) :464-466
[4]   Enzyme therapy for management of coeliac disease [J].
Cornell, HJ ;
Macrae, FA ;
Melny, J ;
Pizzey, CJ ;
Cook, F ;
Mason, S ;
Bhathal, PS ;
Stelmasiak, T .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2005, 40 (11) :1304-1312
[5]   No genetic association of the human prolyl endopeptidase gene in the Dutch celiac disease population [J].
Diosdado, B ;
Stepniak, DT ;
Monsuur, AJ ;
Franke, L ;
Wapenaar, MC ;
Mearin, ML ;
Koning, F ;
Wijmenga, C .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2005, 289 (03) :G495-G500
[6]  
FRAZER AC, 1959, LANCET, V2, P252
[7]   Effect of barley endoprotease EP-B2 on gluten digestion in the intact rat [J].
Gass, Jonathan ;
Vora, Harmit ;
Bethune, Michael T. ;
Gray, Gary M. ;
Khosla, Chaitan .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2006, 318 (03) :1178-1186
[8]   A direct role for NKG2D/MICA interaction in villous atrophy during celiac disease [J].
Hüe, S ;
Mention, JJ ;
Monteiro, RC ;
Zhang, SL ;
Cellier, C ;
Schmitz, J ;
Verkarre, V ;
Fodil, N ;
Bahram, S ;
Cerf-Bensussan, N ;
Caillat-Zucman, S .
IMMUNITY, 2004, 21 (03) :367-377
[9]   Association between innate response to gliadin and activation of pathogenic T cells in coeliac disease [J].
Maiuri, L ;
Ciacci, C ;
Ricciardelli, I ;
Vacca, L ;
Raia, V ;
Auricchio, S ;
Picard, J ;
Osman, M ;
Quaratino, S ;
Londei, M .
LANCET, 2003, 362 (9377) :30-37
[10]   Alterations of the intestinal transport and processing of gliadin peptides in celiac disease [J].
Matysiak-Budnik, T ;
Candalh, C ;
Dugave, C ;
Namane, A ;
Cellier, C ;
Cerf-Bensussan, N ;
Heyman, M .
GASTROENTEROLOGY, 2003, 125 (03) :696-707