Tsuneyama K, Van De Water J, Yamazaki K, Suzuki K, Sato S, Takeda Y, Ruebner B, Yost B A, Nakanuma Y, Coppel R L, Gershwin M E
Department of Pathology, Kanazawa University School of Medicine, Japan.
Autoimmunity. 1997;26(1):23-31. doi: 10.3109/08916939709009547.
Primary biliary cirrhosis (PBC) is an autoimmune liver disease of unknown etiology. Nearly 93% of patients with PBC exhibit evidence of focal sialoadenitis. In an earlier study, we reported evidence of aberrant expression of PDC-E2, or a mimeotope, in the salivary glands of patients with PBC that had Sjogren's syndrome. At the time of the previous study, data was not yet available regarding patients with PBC without sicca complaints. Therefore, to investigate the extent of salivary gland involvement in PBC, we collected lip biopsy sections from 9 PBC patients diagnosed as PBC by liver biopsy, without clinical or histologic features of Sjogren's syndrome and 9 PBC patients with established Sjogren's syndrome. Using immunohistochemical staining with both a murine monoclonal antibody. C355.1, and a human combinatorial antibody, SP4, we examined the ducts of these salivary glands for the presence of the characteristic aberrant staining pattern found in patients with PBC. We report that 6/9 PBC patients fulfilling established Sjogren's syndrome criteria and 6/9 PBC patients lacking features of Sjogren's syndrome showed intense staining of the ductal epithelial cells of the salivary gland. These data suggest that the PBC-specific antigen recognized by C355.1 and SP4 in bile duct epithelial cells is expressed aberrantly in the salivary gland in 66% of patients with PBC, independent of Sjogren's syndrome. This finding suggests a common disease process in these two tissues. Further, expression of this molecule may be an early marker of salivary gland involvement in patients with PBC.
原发性胆汁性肝硬化(PBC)是一种病因不明的自身免疫性肝病。近93%的PBC患者有局灶性涎腺炎的证据。在一项早期研究中,我们报告了患有干燥综合征的PBC患者唾液腺中丙酮酸脱氢酶E2(PDC-E2)或其模拟表位异常表达的证据。在之前的研究时,尚无关于无干燥症状的PBC患者的数据。因此,为了研究PBC患者唾液腺受累的程度,我们收集了9例经肝活检诊断为PBC、无干燥综合征临床或组织学特征的患者以及9例已确诊干燥综合征的PBC患者的唇活检切片。使用鼠单克隆抗体C355.1和人组合抗体SP4进行免疫组化染色,我们检查了这些唾液腺导管,以寻找PBC患者中发现的特征性异常染色模式。我们报告,6/9符合已确立的干燥综合征标准的PBC患者和6/9无干燥综合征特征的PBC患者唾液腺导管上皮细胞显示强烈染色。这些数据表明,C355.1和SP4在胆管上皮细胞中识别的PBC特异性抗原在66%的PBC患者唾液腺中异常表达,与干燥综合征无关。这一发现提示这两种组织中存在共同的疾病过程。此外,该分子的表达可能是PBC患者唾液腺受累的早期标志物。