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循环中形成的IgA免疫复合物的肝胆清除。

Hepatobiliary clearance of IgA immune complexes formed in the circulation.

作者信息

Harmatz P R, Kleinman R E, Bunnell B W, Bloch K J, Walker W A

出版信息

Hepatology. 1982 May-Jun;2(3):328-33. doi: 10.1002/hep.1840020307.

Abstract

The formation and clearance of circulating IgA immune complexes from blood to bile was investigated in this study. The i.v. injection of either MOPC-315, an IgA M-component with antidinitrophenyl (DNP) specificity, or TEPC-15, an IgA M-component of a different specificity, was followed by i.v. injection of 125I-DNP10-bovine serum albumin (BSA) as the antigen. The formation and clearance of IgA immune complexes in the circulation of MOPC-315-treated, but not TEPC-15-treated animals was demonstrated by immunoprecipitation with polyacrylamide beads coated with rabbit anti-mouse IgA. IgA-125I-DNP10-BSA complexes were identified in the bile from MOPC-315-treated, but not TEPC-15-treated animals utilizing this same immunoprecipitation technique. These observations suggest that the liver or bile ducts transport IgA immune complexes from blood into bile. The clearance of 125I-DNP10-BSA from the circulation was documented by coprecipitation with rabbit anti-BSA and BSA. The clearance of this circulating antigen was slower in the MOPC-315-treated than in the TEPC-15-treated animals suggesting that under the conditions of the present experiment, circulating antigen is cleared more slowly after IgA immune complex formation.

摘要

本研究对循环IgA免疫复合物从血液到胆汁的形成及清除过程进行了研究。静脉注射具有抗二硝基苯基(DNP)特异性的IgA M成分MOPC-315或具有不同特异性的IgA M成分TEPC-15后,再静脉注射125I-DNP10-牛血清白蛋白(BSA)作为抗原。用包被兔抗小鼠IgA的聚丙烯酰胺珠进行免疫沉淀,结果表明,在MOPC-315处理而非TEPC-15处理的动物循环中,IgA免疫复合物得以形成并清除。利用相同的免疫沉淀技术,在MOPC-315处理而非TEPC-15处理的动物胆汁中鉴定出了IgA-125I-DNP10-BSA复合物。这些观察结果表明,肝脏或胆管可将IgA免疫复合物从血液转运至胆汁中。通过与兔抗BSA和BSA共沉淀记录了125I-DNP10-BSA从循环中的清除情况。在MOPC-315处理的动物中,这种循环抗原的清除比TEPC-15处理的动物更慢,这表明在本实验条件下,IgA免疫复合物形成后,循环抗原的清除更慢。

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