Leptin M, Melchers F
J Immunol Methods. 1983 Apr 15;59(1):53-61. doi: 10.1016/0022-1759(83)90145-x.
A panel of monoclonal rat antibodies binding to mouse mu heavy chain were tested for their ability to inhibit the formation of antigen-specific plaques in the hemolytic plaque assay. Nine antibodies inhibited SRC-specific direct IgM plaques at high concentrations (greater than 20 micrograms/ml). In contrast to all others, however, one antibody inhibited these plaques at much lower concentrations (down to 0.4 microgram/ml) when added to the assay. This antibody also inhibited plaques formed by cells secreting antibodies against trinitrophenyl or phosphorylcholine determinants. IgG plaques with any of the above specificities were not inhibited. IgM secretion was unaffected by the monoclonal anti-mu antibody. Its inhibitory effect on plaque formation rather appears to be a consequence of its ability to inhibit complement dependent, IgM mediated lysis of erythrocytes. This monoclonal anti-IgM antibody therefore provides a convenient reagent to distinguish specific direct IgM plaques from indirect IgG plaques.
检测了一组与小鼠μ重链结合的单克隆大鼠抗体在溶血空斑试验中抑制抗原特异性空斑形成的能力。九种抗体在高浓度(大于20微克/毫升)时抑制SRC特异性直接IgM空斑。然而,与所有其他抗体不同的是,有一种抗体在加入试验时,能在低得多的浓度(低至0.4微克/毫升)下抑制这些空斑。该抗体还抑制由分泌针对三硝基苯或磷酰胆碱决定簇的抗体的细胞形成的空斑。具有上述任何特异性的IgG空斑均未被抑制。IgM分泌不受单克隆抗μ抗体的影响。它对空斑形成的抑制作用似乎是其抑制补体依赖性、IgM介导的红细胞裂解能力的结果。因此,这种单克隆抗IgM抗体提供了一种方便的试剂,可用于区分特异性直接IgM空斑和间接IgG空斑。