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针对来自暴露于甲苯二异氰酸酯蒸汽的小鼠的半抗原化蛋白质的单克隆抗体。

Monoclonal antibodies against toluene diisocyanate haptenated proteins from vapor-exposed mice.

作者信息

Ruwona Tinashe B, Johnson Victor J, Schmechel Detlef, Simoyi Reuben H, Beezhold Donald, Siegel Paul D

机构信息

Allergy and Clinical Immunology, National Institute for Occupational Safety and Health, Morgantown, West Virginia 26505-2888, USA.

出版信息

Hybridoma (Larchmt). 2010 Jun;29(3):221-9. doi: 10.1089/hyb.2009.0110.

Abstract

Toluene diisocyanate (TDI) is an industrially important polymer cross-linker used in the production of polyurethane. Workplace exposure to TDI and other diisocyanates is reported to be a leading cause of low molecular weight-induced occupational asthma (OA). Currently we have a limited understanding of the pathogenesis of OA. Monoclonal antibodies (MAbs) that recognize TDI bound proteins would be valuable tools/reagents, both in exposure monitoring and in TDI-induced asthma research. We sought to develop toluene diisocyanate (TDI)-specific MAbs for potential use in the development of standardized immunoassays for exposure and biomarker assessments. Mice were exposed 4 h/day for 12 consecutive weekdays to 50 ppb, 2,4;2,6 TDI vapor (80/20 mixture). Splenocytes were isolated 24 h after the last exposure for hybridoma production. Hybridomas were screened in a solid-phase indirect enzyme-linked immunosorbent assay (ELISA) against a 2,4 TDI-human serum albumin (2,4 TDI-HSA) protein conjugate. Three hybridomas producing 2,4 TDI-HSA reactive IgM MAbs were obtained. The properties of these MAbs (isotype and reactivity to various protein-isocyanate conjugate epitopes) were characterized using ELISA, dot blot, and Western blot analyses. Western blot analyses demonstrated that some TDI conjugates form inter- and intra-molecular links, resulting in multimers and a change in the electrophoretic mobility of the conjugate. These antibodies may be useful tools for the isolation of endogenous diisocyanate-modified proteins after natural or experimental exposures and for characterization of the toxicity of specific dNCOs.

摘要

甲苯二异氰酸酯(TDI)是一种在工业上重要的聚合物交联剂,用于生产聚氨酯。据报道,工作场所接触TDI和其他二异氰酸酯是低分子量诱导的职业性哮喘(OA)的主要原因。目前,我们对OA的发病机制了解有限。识别与TDI结合蛋白的单克隆抗体(MAb)在暴露监测和TDI诱导的哮喘研究中都是有价值的工具/试剂。我们试图开发针对甲苯二异氰酸酯(TDI)的特异性单克隆抗体,以用于开发标准化免疫测定法进行暴露和生物标志物评估。小鼠连续12个工作日每天暴露4小时,接触浓度为50 ppb的2,4;2,6 TDI蒸汽(80/20混合物)。在最后一次暴露24小时后分离脾细胞用于制备杂交瘤。在固相间接酶联免疫吸附测定(ELISA)中,用2,4 TDI-人血清白蛋白(2,4 TDI-HSA)蛋白偶联物筛选杂交瘤。获得了三种产生与2,4 TDI-HSA反应性IgM单克隆抗体的杂交瘤。使用ELISA、斑点印迹和蛋白质印迹分析对这些单克隆抗体的特性(亚型以及对各种蛋白质-异氰酸酯偶联表位的反应性)进行了表征。蛋白质印迹分析表明,一些TDI偶联物形成分子间和分子内连接,导致多聚体形成以及偶联物电泳迁移率的变化。这些抗体可能是用于在自然或实验暴露后分离内源性二异氰酸酯修饰蛋白以及表征特定二异氰酸酯毒性的有用工具。

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