Reilly T M, Knabb R M, Chiu A T, Bradfute D L, Timmermans P B
E.I. du Pont de Nemours and Company, Medical Products Department, Wilmington, Delaware 19880-0400.
Thromb Haemost. 1989 Apr 25;61(2):259-61.
Three murine monoclonal antibodies to tissue-type plasminogen activator (t-PA) were evaluated for their effects on the binding of iodinated t-PA to cultured human hepatoma cells (Hep G2), and on extending the half-life of t-PA injected into rabbits. Two of the antibodies, AE5 and EG2, significantly inhibited t-PA binding in vitro, and extended the in vivo half-life of t-PA four to five-fold. A third antibody, BA10, which had a much smaller inhibitory effect on t-PA binding, had no influence in extending t-PA's half-life. MOPC-21, a control antibody not directed to t-PA, had no effect on either test. Our results are the first to correlate different compounds' effects on t-PA binding with their ability to retard t-PA clearance in vivo, and provide additional evidence for the importance of a liver cell receptor in the t-PA clearance process.
评估了三种针对组织型纤溶酶原激活剂(t-PA)的鼠单克隆抗体,它们对碘化t-PA与培养的人肝癌细胞(Hep G2)的结合以及对延长注入兔子体内的t-PA半衰期的影响。其中两种抗体AE5和EG2在体外显著抑制t-PA的结合,并将t-PA的体内半衰期延长了四至五倍。第三种抗体BA10对t-PA结合的抑制作用要小得多,对延长t-PA的半衰期没有影响。MOPC-21是一种不针对t-PA的对照抗体,对两项测试均无影响。我们的结果首次将不同化合物对t-PA结合的影响与其在体内延缓t-PA清除的能力相关联,并为肝细胞受体在t-PA清除过程中的重要性提供了额外证据。