Harkiss G D, Hendrie F, Nuki G
Clin Immunol Immunopathol. 1987 Sep;44(3):283-96. doi: 10.1016/0090-1229(87)90072-9.
Antibodies to DNA and K30p were purified by affinity procedures and tested for their ability to cross-react with K30p and DNA, respectively. Anti-ssDNA antibodies were shown to react with solid-phase K30p and be inhibited in a dose-dependent manner by soluble ssDNA and K30p. Conversely, anti-K30p antibodies were found to bind immobilized ssDNA and be inhibited with soluble inhibitor. These results show that certain subpopulations of anti-ssDNA and anti-K30p antibodies overlap in their ligand-binding specificities. Idiotypic (Id) analysis showed that anti-K30p antibodies did not react significantly with an anti-Id reagent directed against a common anti-DNA framework Id (AM Id), thus clearly separating K30p-binding anti-DNA antibodies into an AM Id-negative population. When anti-DNA antibodies were probed with an anti-Id reagent directed against a framework Id present on anti-K30p antibodies (SP Id), substantial reactivity was found. Thus the SP Id identifies a subpopulation of antibodies capable of binding both K30p and DNA. These results show that a subset of anti-ssDNA antibodies cross-react with K30p antigen and are idiotypically related to a subset of antibodies reactive with K30p.
通过亲和程序纯化了针对DNA和K30p的抗体,并分别检测它们与K30p和DNA交叉反应的能力。抗单链DNA抗体显示与固相K30p反应,并被可溶性单链DNA和K30p以剂量依赖性方式抑制。相反,发现抗K30p抗体与固定化单链DNA结合,并被可溶性抑制剂抑制。这些结果表明,抗单链DNA和抗K30p抗体的某些亚群在其配体结合特异性上存在重叠。独特型(Id)分析表明,抗K30p抗体与针对常见抗DNA框架Id(AM Id)的抗Id试剂没有明显反应,从而将结合K30p的抗DNA抗体明确分为AM Id阴性群体。当用针对抗K30p抗体上存在的框架Id(SP Id)的抗Id试剂检测抗DNA抗体时,发现有显著反应性。因此,SP Id识别出能够结合K30p和DNA的抗体亚群。这些结果表明,一部分抗单链DNA抗体与K30p抗原交叉反应,并且在独特型上与一部分与K30p反应的抗体相关。