Division of Liver Diseases, Mount Sinai School of Medicine, New York, NY 10029, USA.
J Virol Methods. 2011 Jan;171(1):169-75. doi: 10.1016/j.jviromet.2010.10.020. Epub 2010 Oct 27.
Many anti-HCV antibodies are available, but more are needed for research and clinical applications. This study examines whether ascitic fluid from cirrhotic patients could be a source of reagent-grade antibodies. Ascitic fluid from 29 HCV patients was screened by ELISA for anti-HCV antibodies against three viral proteins: core, NS4B, and NS5A. Significant patient-to-patient variability in anti-HCV antibody titers was observed. Total ascitic fluid IgG purified by Protein-A chromatography reacted with HCV proteins in immunoblots, cell extracts, and replicon-expressing cells. Affinity-purification using synthetic peptides as bait allowed the preparation of cross-genotypic antibodies directed against pre-selected regions of HCV core, NS4B, and NS5A proteins. The performance of the polyclonal antibodies was comparable to that of monoclonal antibodies. Anti-NS4B antibody preparations reacted with genotype 1a, 1b, and 2a NS4B proteins in immunoblots and allowed NS4B to be localized in replicon-expressing cells. Ascitic fluid is an abundant source of human polyclonal cross-genotypic antibodies that can be used as an alternative to blood. This study shows the utility of selectively purifying human polyclonal antibodies from ascitic fluid. Affinity purification allows antibodies to be selected that are comparable to monoclonal antibodies in their ability to react with targeted regions of viral proteins.
许多抗 HCV 抗体可用于临床诊断,但研究和临床应用仍需要更多的抗体。本研究旨在探讨肝硬化患者腹水能否成为试剂级抗体的来源。采用 ELISA 法对 29 例 HCV 患者的腹水进行检测,以鉴定针对 HCV 核心、NS4B 和 NS5A 三种蛋白的抗体。结果发现,患者之间的抗 HCV 抗体滴度存在显著差异。腹水 IgG 经 Protein-A 层析柱纯化后,与免疫印迹、细胞提取物和表达复制子的细胞中的 HCV 蛋白发生反应。用合成肽作为诱饵进行亲和纯化,可制备针对 HCV 核心、NS4B 和 NS5A 蛋白选定区域的交叉基因型抗体。这些多克隆抗体的性能与单克隆抗体相当。抗 NS4B 抗体与免疫印迹中的 1a、1b 和 2a 基因型 NS4B 蛋白反应,并能使 NS4B 在表达复制子的细胞中定位。腹水是人类交叉基因型多克隆抗体的丰富来源,可替代血液用于检测。本研究表明,选择性从腹水纯化人多克隆抗体具有实际应用价值。亲和纯化可以选择与单克隆抗体具有相似反应性的抗体,用于鉴定病毒蛋白的靶向区域。