Sobieska M, Fassbender K, Aeschlimann A, Bourgeois P, Mackiewicz S, Müller W
Department of Rheumatology, University of Medical Sciences, Poznań, Poland.
Clin Rheumatol. 1998;17(3):258-60. doi: 10.1007/BF01451062.
Crossed affinoimmunoelectrophoresis with Con A as a ligand was used to examine the microheterogeneity of alpha1-acid glycoprotein (AGP) and alpha1-antichymotrypsin (ACT) in sera of patients with child-onset and adult-onset Still's disease. The reactivity of both proteins was increased in sera of adults and decreased in sera of children with active disease, when compared with normal values. We also found statistically significant differences in serum concentration of ACT and ferritin in both diseases. This result suggests different pathogenic mechanisms of Still's disease in children and adults. Serum concentration of ferritin and ACT could be of value as a combined marker for the adult, but not the juvenile form of Still's disease.
以伴刀豆球蛋白A作为配体的交叉亲和免疫电泳,用于检测儿童期和成人期斯蒂尔病患者血清中α1-酸性糖蛋白(AGP)和α1-抗糜蛋白酶(ACT)的微观异质性。与正常值相比,在患有活动性疾病的成人血清中,这两种蛋白质的反应性增加,而在儿童血清中则降低。我们还发现,在这两种疾病中,ACT和铁蛋白的血清浓度存在统计学上的显著差异。这一结果表明,儿童和成人斯蒂尔病的致病机制不同。铁蛋白和ACT的血清浓度,作为成人斯蒂尔病而非青少年型斯蒂尔病的联合标志物,可能具有一定价值。