Goodall A H, Meek F L, Waters J A, Miescher G C, Janossy G, Thomas H C
J Immunol Methods. 1982 Jul 30;52(2):167-74. doi: 10.1016/0022-1759(82)90042-4.
A two-site antigen assay for HBsAg has been developed that employs 3 monoclonal antibodies. The antibodies were selected for their high affinity and their particular epitope specificity to establish an assay with a sensitivity for the antigen comparable with that of a conventional assay with heterologous antisera. In addition, by selecting a monoclonal antibody for use as a tracer which does not compete for antigenic binding sites with the solid-phase monoclonal antibodies, it has been possible to perform a two-site assay in a single 1 h incubation step, achieving the same degree of sensitivity. This principle of using monoclonal antibodies in a one-step assay therefore gives advantages of speed and simplicity over assays using heterologous antisera and would be applicable to a variety of antigen assays for which appropriate monoclonal antibodies are available.
已开发出一种用于检测乙肝表面抗原(HBsAg)的双位点抗原检测法,该方法采用了3种单克隆抗体。这些抗体因其高亲和力和特定的表位特异性而被选中,以建立一种对该抗原的检测灵敏度与使用异种抗血清的传统检测法相当的检测方法。此外,通过选择一种用作示踪剂的单克隆抗体,该抗体不会与固相单克隆抗体竞争抗原结合位点,从而有可能在单个1小时孵育步骤中进行双位点检测,达到相同程度的灵敏度。因此,在一步检测中使用单克隆抗体的这一原理相对于使用异种抗血清的检测法具有速度快和操作简单的优点,并且适用于有合适单克隆抗体可用的各种抗原检测。