Fais S, Maiuri L, Pallone F, De Vincenzi M, De Ritis G, Troncone R, Auricchio S
Cattedra di Gastroenterologia, Università di Roma, Italy.
Gut. 1992 Apr;33(4):472-5. doi: 10.1136/gut.33.4.472.
Jejunal biopsies from 16 treated coeliac disease patients and from nine controls were cultured with and without a peptic-tryptic digest of gliadin. Cultures with a peptic-tryptic digest of maize prolamins were also undertaken. Frozen sections of baseline and cultured mucosa were stained by immunofluorescence with an anti-HLA-DR monoclonal antibody. Before culture the villous epithelium from both controls and treated coeliac disease expressed DR molecules while the crypt epithelium did not. When biopsies from treated coeliac disease were cultured with gliadin the expression of DR was enhanced in the crypt epithelium in eight of 14 cultures and in 11 of 14 was reduced or absent on the villous epithelium. No change was observed in control cultures. We conclude that gliadin is capable of inducing HLA-DR on the crypt epithelium of in vitro cultured coeliac disease mucosa, providing indirect evidence that gliadin may activate cell mediated immune mechanisms within the small bowel mucosa. This model could prove useful in identifying the immunogenic sequence(s) of gliadins and related prolamins.
对16例接受治疗的乳糜泻患者和9例对照者的空肠活检组织进行培养,分别加入和不加入麦醇溶蛋白的胃蛋白酶 - 胰蛋白酶消化物。同时也进行了玉米醇溶蛋白胃蛋白酶 - 胰蛋白酶消化物的培养。用抗HLA - DR单克隆抗体通过免疫荧光对基线和培养后的黏膜冰冻切片进行染色。培养前,对照者和接受治疗的乳糜泻患者的绒毛上皮均表达DR分子,而隐窝上皮不表达。当用麦醇溶蛋白培养接受治疗的乳糜泻患者的活检组织时,14个培养物中有8个隐窝上皮的DR表达增强,14个中有11个绒毛上皮的DR表达减少或缺失。对照培养物中未观察到变化。我们得出结论,麦醇溶蛋白能够在体外培养的乳糜泻黏膜隐窝上皮诱导HLA - DR表达,间接证明麦醇溶蛋白可能激活小肠黏膜内的细胞介导免疫机制。该模型可能有助于确定麦醇溶蛋白和相关醇溶蛋白的免疫原性序列。