Gur H, Shen G, Sutjita M, Terrberry J, Alosachie I, Barka N, Lin H C, Peter J B, Meroni P L, Kaplan M
Department of Medicine, Sheba Medical Center, Tel Hashomer, Israel.
Pathobiology. 1995;63(2):76-82. doi: 10.1159/000163937.
Primary sclerosing cholangitis (PSC) is a chronic progressive liver disease of unknown etiology. It has been suggested that genetic and immunological factors are important in its pathogenesis. The present study examined the prevalence of 23 different autoantibodies in 25 PSC sera, by ELISA, in order to better define the autoimmune profile of PSC. The results indicate that 88% of PSC patients produced at least 1 autoantibody, and 36% had reactivity to multiple autoantibodies. Moreover, 35% of the PSC patients produced anti-endothelial-cell antibodies (AECA) and 75% of the sera contained perinuclear antineutrophil cytoplasmic antibodies (pANCA), detected by indirect immunofluorescence. The prominent ANCA autoantibody was anti-cathepsin-G, demonstrated in 35% of the patients. The multiplicity of the autoantibody profile, revealed in the present study, points to the autoimmune characteristics of PSC. In addition, the association of ANCA and of AECA in PSC may suggest a pathogenic role for these antibodies in PSC.
原发性硬化性胆管炎(PSC)是一种病因不明的慢性进行性肝病。有人认为遗传和免疫因素在其发病机制中起重要作用。本研究通过酶联免疫吸附测定(ELISA)检测了25份PSC血清中23种不同自身抗体的流行情况,以便更好地界定PSC的自身免疫特征。结果表明,88%的PSC患者至少产生1种自身抗体,36%的患者对多种自身抗体有反应。此外,通过间接免疫荧光检测,35%的PSC患者产生抗内皮细胞抗体(AECA),75%的血清含有核周抗中性粒细胞胞浆抗体(pANCA)。突出的ANCA自身抗体是抗组织蛋白酶G,在35%的患者中检测到。本研究揭示的自身抗体谱的多样性表明PSC具有自身免疫特征。此外,PSC中ANCA和AECA的关联可能提示这些抗体在PSC中具有致病作用。