Paediatric Research Centre, Medical School, University of Tampere, Tampere 33014, Finland.
Clin Exp Immunol. 2011 Apr;164(1):127-36. doi: 10.1111/j.1365-2249.2010.04317.x. Epub 2011 Jan 14.
In coeliac disease, the intake of dietary gluten induces small-bowel mucosal damage and the production of immunoglobulin (Ig)A class autoantibodies against transglutaminase 2 (TG2). We examined the effect of coeliac patient IgA on the apical-to-basal passage of gluten-derived gliadin peptides p31-43 and p57-68 in intestinal epithelial cells. We demonstrate that coeliac IgA enhances the passage of gliadin peptides, which could be abolished by inhibition of TG2 enzymatic activity. Moreover, we also found that both the apical and the basal cell culture media containing the immunogenic gliadin peptides were able to induce the proliferation of deamidation-dependent coeliac patient-derived T cells even in the absence of exogenous TG2. Our results suggest that coeliac patient IgA could play a role in the transepithelial passage of gliadin peptides, a process during which they might be deamidated.
在乳糜泻中,膳食 gluten 的摄入会导致小肠黏膜损伤,并产生针对转谷氨酰胺酶 2 (TG2) 的免疫球蛋白 (Ig)A 类自身抗体。我们研究了乳糜泻患者 IgA 对肠上皮细胞中 gluten 衍生的gliadin 肽 p31-43 和 p57-68 从顶端到基底的传递的影响。我们证明乳糜泻 IgA 增强了 gliadin 肽的传递,而这一传递可以通过抑制 TG2 酶活性来消除。此外,我们还发现,含有免疫原性 gliadin 肽的顶端和基底细胞培养基都能够诱导脱酰胺依赖性乳糜泻患者源性 T 细胞的增殖,即使没有外源性 TG2 也是如此。我们的结果表明,乳糜泻患者 IgA 可能在 gliadin 肽的跨上皮传递中发挥作用,在此过程中它们可能被脱酰胺。