Sakaguchi K
Gastroenterol Jpn. 1983 Aug;18(4):330-8. doi: 10.1007/BF02774950.
Anti-liver-specific membrane lipoprotein (anti-LP-1) and anti-Tamm-Horsfall glycoprotein (anti-THGP) rabbit antibodies were found to bind to Chang liver cells, a cultured human hepatocyte cell line, and PLC/PRF/5, a hepatoma cell line. The antibodies bound were determined by an immunofluorescence staining and a semiquantitative 125I-protein A binding assay. The 125I-protein A binding assay was successfully adapted to determine anti-hepatocyte plasma membrane antibodies in sera of patients with lupoid hepatitis and chronic active hepatitis. The percentage of 125I-protein A bound in 10 normal subjects were 1.5 +/- 0.4 (mean +/- standard deviation) for PLC/PRF/5 and 1.6 +/- 0.6 for Chang liver cell, while those in 2 patients with lupoid hepatitis were 7.2 +/- 0.3, 5.9 +/- 0.1, and those in 8 patients with chronic active hepatitis 3.9 +/- 1.3, 3.2 +/- 1.5, respectively. Furthermore, a blocking study revealed that LP-1 and THGP were partially involved in antigen sites recognized with anti-hepatocyte plasma membrane antibodies in sera of a patient with lupoid hepatitis. The retaining ability of antibody binding to the hepatocytes after the absorption with non-hepatocyte cells suggested the presence of antibodies specific for the hepatocyte plasma membrane in the patient's serum.
抗肝特异性膜脂蛋白(抗LP - 1)和抗Tamm - Horsfall糖蛋白(抗THGP)兔抗体被发现可与Chang肝细胞(一种培养的人肝细胞系)和PLC/PRF/5(一种肝癌细胞系)结合。通过免疫荧光染色和125I - 蛋白A结合的半定量测定来确定结合的抗体。125I - 蛋白A结合测定成功用于检测类狼疮性肝炎和慢性活动性肝炎患者血清中的抗肝细胞质膜抗体。10名正常受试者中,PLC/PRF/5细胞的125I - 蛋白A结合百分比为1.5±0.4(平均值±标准差),Chang肝细胞为1.6±0.6;而2名类狼疮性肝炎患者的分别为7.2±0.3、5.9±0.1,8名慢性活动性肝炎患者的分别为3.9±1.3、3.2±1.5。此外,一项阻断研究表明,LP - 1和THGP部分参与了类狼疮性肝炎患者血清中抗肝细胞质膜抗体识别的抗原位点。用非肝细胞吸收后抗体与肝细胞结合的保留能力表明患者血清中存在对肝细胞质膜特异的抗体。