Taylor R P, Horgan C
Mol Immunol. 1984 Oct;21(10):853-62. doi: 10.1016/0161-5890(84)90139-1.
We have investigated quantitatively the complement-mediated binding of prepared, soluble 125I-7S IgG antibody/3H-dsDNA immune complexes to human red blood cells (RBCs). We have performed these studies by using a detailed modification of the RBC-CF assay [Pedersen et al., J. Immun. Meth. 38, 269-280 (1980)] which now allows for the simultaneous measurement of both 3H-DNA and 125I-binding to the cells. Our results indicate that, in the case of three SLE patients, their anti-dsDNA antibody titers are sufficiently high that a small fraction of their 125I-7S IgG antibodies (ca 0.1-0.2%) can be identified as specifically anti-dsDNA. We have also used an indirect method (with 125I-labelled rabbit anti-human IgG) for the determination of IgG anti-dsDNA antibodies in complement-fixing antibody/dsDNA immune complexes that bind to RBCs, and the results of these measurements are in reasonable agreement with the direct binding experiments. These studies have also allowed us to estimate the antibody/DNA stoichiometries in complement-fixing immune complexes. The results of these experiments may provide a useful standard for the analysis of monoclonal anti-dsDNA antibodies.
我们已经定量研究了制备好的可溶性125I-7S IgG抗体/3H-双链DNA免疫复合物通过补体介导与人红细胞(RBC)的结合。我们通过对红细胞补体结合试验(RBC-CF试验)[Pedersen等人,《免疫学方法杂志》38,269 - 280(1980)]进行详细改进来开展这些研究,该改进后的试验现在能够同时测量3H-DNA和125I与细胞的结合情况。我们的结果表明,对于三名系统性红斑狼疮(SLE)患者而言,他们的抗双链DNA抗体滴度足够高,以至于其一小部分125I-7S IgG抗体(约0.1 - 0.2%)可被鉴定为特异性抗双链DNA抗体。我们还使用了一种间接方法(用125I标记的兔抗人IgG)来测定与RBC结合的补体固定抗体/双链DNA免疫复合物中的IgG抗双链DNA抗体,这些测量结果与直接结合实验结果合理相符。这些研究还使我们能够估计补体固定免疫复合物中的抗体/DNA化学计量比。这些实验结果可能为单克隆抗双链DNA抗体的分析提供一个有用的标准。