In vitro activities of A-gliadin-related synthetic peptides - Damaging effect on the atrophic coeliac mucosa and activation of mucosal immune response in the treated coeliac mucosa

被引:92
作者
Maiuri, L
Troncone, R
Mayer, M
Coletta, S
Picarelli, A
DeVincenzi, M
Pavone, V
Auricchio, S
机构
[1] UNIV NAPLES FEDERICO II,DEPT CHEM,I-80131 NAPLES,ITALY
[2] UNIV ROMA LA SAPIENZA,MED CLIN 2,DEPT GASTROENTEROL,ROME,ITALY
[3] IST SUPER SANITA,LAB METAB & PATHOL BIOCHEM,I-00161 ROME,ITALY
关键词
coeliac disease; gliadin; mucosal immunity; organ culture;
D O I
10.3109/00365529609004874
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Gliadin amino acid sequence(s) responsible for toxicity in susceptible individuals have nor been fully elucidated. Previous in vitro studies have suggested the presence of active sequences in the NH2-terminal part of the A-gliadin molecule. In this paper the in vitro activity of A-gliadin synthetic peptides 31-55, 31-43, and 44-55 has been investigated. Methods: Organ culture of jejunal mucosa from untreated and treated coeliac patients was used. In the first system enterocyte height was used as a measure of peptide toxicity; in the second system evidence of activated mucosal cell-mediated immune response was sought. Results: Peptides 31-55 and 31-43 were active on untreated coeliac mucosa at a concentration of 0.5 mg/ml and peptide 44-55 only at a concentration of 3 mg/ml. In in vitro-cultured treated coeliac mucosa peptides 31-55 and 31-43 at 1 mg/ml and peptide 44-55 at 3 mg/ml were able to induce enhanced epithelial expression of HLA-DR and 4F2 molecules and the appearance of CD25-positive cells. Conclusions: Our results suggest that 31-43 and 44-55 A-gliadin peptides are both active, even if to different extents. In vitro systems remain essential tools to screen material to be subsequently tested in vivo.
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页码:247 / 253
页数:7
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