Taylor R P, Andrews B S, Morley K W, Conlon T
Rheumatol Int. 1981;1(1):29-34. doi: 10.1007/BF00541220.
We have prepared antibody/3H-dsDNA immune complexes and have used three independent radioimmunoassays to quantitate their interaction with complement; the solution phase C1q assay, the Raji cell assay, and a complement-based red blood cell adherence assay (RBC-CF). Our results indicate that although there is reasonable qualitative agreement between the Raji cell assay and the RBC-CF assay, there are some differences in the quantitative range of sensitivities of the two assays. On the other hand, we find that most of the complement-fixing antibody/3H-dsDNA complexes are not detected in the solution phase C1q assay. The results suggest this is because the absolute concentrations of the immune complexes were too low to achieve significant precipitation under the standard conditions used in the C1q assay. The implication of these findings with respect to the potential detection and analysis of antibody/dsDNA immune complexes is discussed.
我们制备了抗体/³H -双链DNA免疫复合物,并使用三种独立的放射免疫测定法来定量其与补体的相互作用;即液相C1q测定法、拉吉细胞测定法和基于补体的红细胞黏附测定法(RBC - CF)。我们的结果表明,尽管拉吉细胞测定法和RBC - CF测定法之间在定性上有合理的一致性,但两种测定法在定量敏感性范围上存在一些差异。另一方面,我们发现在液相C1q测定法中未检测到大多数补体结合抗体/³H -双链DNA复合物。结果表明,这是因为免疫复合物的绝对浓度过低,无法在C1q测定法所使用的标准条件下实现显著沉淀。本文讨论了这些发现对于抗体/双链DNA免疫复合物潜在检测和分析的意义。