Szostecki C, Guldner H H, Will H
Heinrich-Pette-Institu für Experimentelle Virologie und Immunologie, Universität Hamburg, Germany.
Semin Liver Dis. 1997 Feb;17(1):71-8. doi: 10.1055/s-2007-1007184.
Autoantibodies against nuclear proteins are not always but rather frequently present in sera of patients with primary biliary cirrhosis (PBC). The specificity and diagnostic value of these autoantibodies for PBC have only recently become clear through cloning of the cDNA of some of the corresponding autoantigens which allowed the establishment of immunological assays with recombinant autoantigens expressed in E. coli and eukaryotic cells. In this report we summarize primarily the knowledge on the structure and putative function of two nuclear autoantigens, the Sp100 and PML proteins, which are present in so-called nuclear dots (NDs) and against which autoantibodies are present in a subpopulation of PBC patients. Furthermore, the type of autoimmune response (epitope specificity and immunoglobulin class) against both the Sp100 and PML proteins and the specificity of the anti-Sp100 and anti-PML autoantibodies for PBC patients and patients with other autoimmune diseases is reviewed. Current knowledge clearly indicates that determination of anti-Sp100 and anti-PML autoantibodies substantially improves diagnosis of PBC as these autoantibodies are highly specific for this disease even when autoantibodies against mitochondrial antigens, a hallmark of most PBC patients, are not found. The type of autoimmune response against the Sp100 and PML proteins also provides some clues about possible mechanisms which lead to autoantigenicity of both proteins.
原发性胆汁性肝硬化(PBC)患者血清中常存在针对核蛋白的自身抗体,但并非总是如此。这些自身抗体对PBC的特异性和诊断价值,直到最近通过克隆一些相应自身抗原的cDNA才得以明确,这使得利用在大肠杆菌和真核细胞中表达的重组自身抗原建立免疫测定成为可能。在本报告中,我们主要总结了关于两种核自身抗原Sp100和PML蛋白的结构和假定功能的知识,它们存在于所谓的核点(NDs)中,并且在一部分PBC患者体内存在针对它们的自身抗体。此外,还综述了针对Sp100和PML蛋白的自身免疫反应类型(表位特异性和免疫球蛋白类别),以及抗Sp100和抗PML自身抗体对PBC患者和其他自身免疫性疾病患者的特异性。目前的知识清楚地表明,抗Sp100和抗PML自身抗体的检测显著改善了PBC的诊断,因为即使未发现大多数PBC患者的标志性抗线粒体抗原自身抗体,这些自身抗体对该疾病也具有高度特异性。针对Sp100和PML蛋白的自身免疫反应类型也为导致这两种蛋白自身抗原性的可能机制提供了一些线索。