Klotz J L, Minami R M, Teplitz R L
J Immunol Methods. 1979;29(2):155-65. doi: 10.1016/0022-1759(79)90065-6.
A modification of the enzyme-linked immunosorbent assay (ELISA) is described, that permits determination of antibodies to native DNA (nDNA). The same approach can be used to measure antibodies to denatured DNA (dDNA). Poor binding of nDNA to the polystyrene solid phase has presented difficulties in using the ELISA method for assaying anti-nDNA activity (Engvall, 1976), but we find that precoating of the solid phase with protamine sulfate circumvents this problem. Assays for anti-dDNA are also enhanced by the use of protamine sulfate coated tubes. We have used the ELISA method to assay 15 SLE and 27 non-SLE sera for anti-nDNA and anti-dDNA activity. The results are compared with those obtained using the GF/A glass fiber filter assay, previously described by Lewis et al. (1973).
本文描述了一种酶联免疫吸附测定(ELISA)的改良方法,该方法可用于测定抗天然DNA(nDNA)抗体。同样的方法也可用于检测抗变性DNA(dDNA)抗体。nDNA与聚苯乙烯固相的结合较差,这给使用ELISA方法检测抗nDNA活性带来了困难(Engvall,1976),但我们发现用硫酸鱼精蛋白预包被固相可避免这一问题。使用硫酸鱼精蛋白包被的试管也可增强抗dDNA的检测。我们已使用ELISA方法检测了15份系统性红斑狼疮(SLE)血清和27份非SLE血清中的抗nDNA和抗dDNA活性。将结果与Lewis等人(1973年)先前描述的使用GF/A玻璃纤维滤膜测定法获得的结果进行了比较。