Fornasieri A, Sinico R A, Maldifassi P, Bernasconi P, Vegni M, D'Amico G
Br Med J (Clin Res Ed). 1987 Jul 11;295(6590):78-80. doi: 10.1136/bmj.295.6590.78.
Circulating IgA-antigliadin antibodies were detected with enzyme linked immunosorbent assay (ELISA) in four of 121 patients (3%) who had IgA mesangial nephropathy and 14 of 17 children (82%) who had untreated coeliac disease. No positive cases were present in the 54 healthy subjects of the control group. Three patients who had IgA nephropathy and IgA-antigliadin antibodies underwent jejunal biopsy, and two showed mucosal atrophy. In these two patients urinary abnormalities, together with the IgA-antigliadin antibodies, disappeared completely after three months and five months, respectively, of following a gluten free diet. Circulating IgA immune complexes were found in most patients who had coeliac disease and Berger's disease associated with IgA-antigliadin antibodies, suggesting overactivity of the B cells producing IgA in both conditions. By contrast, a circulating IgA rheumatoid factor was detectable in three of the four patients who had IgA nephropathy and asymptomatic coeliac disease but was always absent in children who had coeliac disease but did not show signs of renal disease. These results suggest that a more complex abnormality in the IgA immune response is necessary for renal disease to become manifest in patients who have gluten enteropathy.
采用酶联免疫吸附测定(ELISA)法检测发现,121例患有IgA系膜肾病的患者中有4例(3%)、17例未经治疗的乳糜泻患儿中有14例(82%)存在循环IgA抗麦醇溶蛋白抗体。对照组的54名健康受试者中未出现阳性病例。3例患有IgA肾病且存在IgA抗麦醇溶蛋白抗体的患者接受了空肠活检,其中2例显示黏膜萎缩。在这2例患者中,分别在遵循无麸质饮食3个月和5个月后,尿液异常连同IgA抗麦醇溶蛋白抗体完全消失。在大多数患有乳糜泻且与IgA抗麦醇溶蛋白抗体相关的贝格尔病患者中发现了循环IgA免疫复合物,这表明在这两种情况下产生IgA的B细胞均过度活跃。相比之下,4例患有IgA肾病和无症状乳糜泻的患者中有3例可检测到循环IgA类风湿因子,但在患有乳糜泻但未表现出肾脏疾病迹象的儿童中该因子始终不存在。这些结果表明,对于患有麸质肠病的患者而言,IgA免疫反应中更复杂的异常是肾病显现的必要条件。