Poskitt T R, Poskitt P K
Immunol Commun. 1978;7(5):543-55. doi: 10.3109/08820137809025483.
A radioimmune assay for the detection and quantitation of circulating immune complexes has been developed which employs the L1210 murine leukemia cell. The assay is based upon the binding of immune complexes to the L1210 through its Fc receptor followed by quantitation of the complexes with an 125I-labelled anti-IgG. The radioactivity of the cell pellet is referred to a standard curve generated by incubating the L1210 with known amounts of heat aggregated IgG (AIgG). 7S IgG of three species (human, canine, murine) do not bind significantly to the L1210 in contrast to the respective AIgG. The assay readily distinguishes between sera of healthy individuals and sera of individuals (human and canine) with diseases known to be associated with circulation immune complexes (i.e., systemic lupus erythematosus, HBAg positive acute hepatitis). The L1210 radioimmune assay is capable of detecting as little as 5 micrograms of immune complexes per ml of serum in all three species tested. The assay possesses several advantages over those currently employed, the most notable being the ability of the L1210 cell to detect immune complexes irrespective of their complement fixing properties.
已开发出一种利用L1210小鼠白血病细胞检测和定量循环免疫复合物的放射免疫分析方法。该分析基于免疫复合物通过其Fc受体与L1210结合,随后用125I标记的抗IgG对复合物进行定量。细胞沉淀的放射性与通过将L1210与已知量的热聚集IgG(AIgG)孵育产生的标准曲线相关。与相应的AIgG相比,三种物种(人、犬、小鼠)的7S IgG与L1210的结合不明显。该分析能够轻松区分健康个体的血清和已知与循环免疫复合物相关疾病(即系统性红斑狼疮、HBAg阳性急性肝炎)患者(人和犬)的血清。L1210放射免疫分析在所有测试的三种物种中能够检测到低至每毫升血清5微克的免疫复合物。该分析相对于目前使用的方法具有几个优点,最显著的是L1210细胞能够检测免疫复合物,而不管其补体固定特性如何。