Boyle M D, Langone J J
J Natl Cancer Inst. 1979 Jun;62(6):1537-44.
A method for the quantitative determination of rabbit IgM bound to cell surfaces has been developed. This method was based on the ability of goat IgG specific for rabbit IgM heavy chains to bind 125I-labeled protein A when bound to the antigen. With the use of this technique the production of specific IgM antitumor antibodies in New Zealand White rabbits after immunization with guinea pig hepatoma cells line-1 and line-10 was followed. Differences in the production of IgM were observed between the different bleedings from rabbits immunized with line-1. No significant IgM antibody was produced following immunization of rabbits with line-10 tumor cells. This indirect method for determining IgM on the cell surfaces was objective, easy to perform, and detected complement-fixing and noncomplement-fixing antibodies. In addition, this technique could be applied to quantify other components on the cell surface for which a suitable specific antibody was available.
已开发出一种定量测定与细胞表面结合的兔IgM的方法。该方法基于针对兔IgM重链的山羊IgG在与抗原结合时能够结合125I标记的蛋白A的能力。利用这项技术,追踪了用豚鼠肝癌细胞系-1和系-10免疫的新西兰白兔中特异性IgM抗肿瘤抗体的产生情况。在用系-1免疫的兔子的不同采血样本中观察到了IgM产生的差异。用系-10肿瘤细胞免疫兔子后未产生明显的IgM抗体。这种测定细胞表面IgM的间接方法客观、易于操作,并且能检测补体结合抗体和非补体结合抗体。此外,该技术可用于定量细胞表面其他有合适特异性抗体的成分。