Basso D, Guariso G, Fogar P, Navaglia F, Zambon C-F, Plebani M
Department of Laboratory Medicine, University of Padova, Italy.
Lupus. 2006;15(7):462-5. doi: 10.1191/0961203306lu2334oa.
The present report focuses on the diagnosis of celiac disease and its pathogenesis, which depends on a genetic predisposition (HLA DQ2 or DQ8 haplotypes), gluten ingestion and T cell activation, type II transglutaminase (TG2), the autoantigen recognized by the antiendomysial antibody playing a key role. IgA class antibody anti-environmental (gliadin) and endogenous (TG2) antigens are present in the sera of patients with celiac disease. The anti-TG2 antibody has the best available diagnostic accuracy, especially when measured employing second generation ELISA tests, which use the human TG2 antigen, or immunochemiluminescent assay, which is highly sensitive. A diagnosis of celiac disease must always be confirmed by the histological evaluation of multiple duodenal mucosa specimens, and serology is recommended for follow-up controls.
本报告聚焦于乳糜泻的诊断及其发病机制,其取决于遗传易感性(HLA DQ2或DQ8单倍型)、麸质摄入和T细胞激活,II型转谷氨酰胺酶(TG2)作为抗肌内膜抗体识别的自身抗原发挥关键作用。乳糜泻患者血清中存在针对环境(麦醇溶蛋白)和内源性(TG2)抗原的IgA类抗体。抗TG2抗体具有目前最佳的诊断准确性,尤其是采用使用人TG2抗原的第二代ELISA检测法或高度灵敏的免疫化学发光分析法进行检测时。乳糜泻的诊断必须始终通过多个十二指肠黏膜标本的组织学评估来确认,血清学检测则推荐用于随访监测。