Karounos D G, Pisetsky D S
Immunology. 1987 Apr;60(4):497-501.
The specificity of a panel of murine monoclonal anti-DNA antibodies for DNA antigenic determinants was evaluated by testing their relative binding to various animal and bacterial DNAs. The antibody panel consisted of six monoclonal anti-DNAs of MRL-lpr/lpr and B6-lpr/lpr origin, while the antigens tested were calf thymus (CT), salmon testes (ST), E. coli (EC) and Micrococcus (MC) DNA. While all antibodies bound to CT, ST, and EC DNA to a similar extent by direct ELISA, only one showed an equivalent level of interaction with MC DNA. The relationship of antigenic sites recognized by the antibodies was evaluated further by competition ELISA, assessing the ability of the anti-DNAs to block the interaction of a biotinylated anti-DNA with solid-phase DNA antigen. For each of the DNAs tested, two patterns of DNA interaction could be distinguished on the basis of the relative inhibitory activity of the different monoclonals. These results suggest that anti-DNA antibodies can be characterized using naturally occurring DNAs, with the observed patterns of binding suggesting recognition of unique antigenic sites, some of which are discrete and non-overlapping.
通过检测一组鼠源单克隆抗DNA抗体与各种动物和细菌DNA的相对结合情况,评估了它们对DNA抗原决定簇的特异性。该抗体组由六种源自MRL-lpr/lpr和B6-lpr/lpr的单克隆抗DNA抗体组成,而测试的抗原为小牛胸腺(CT)、鲑鱼精巢(ST)、大肠杆菌(EC)和微球菌(MC)DNA。虽然通过直接ELISA法,所有抗体与CT、ST和EC DNA的结合程度相似,但只有一种抗体与MC DNA的相互作用水平相当。通过竞争ELISA进一步评估抗体识别的抗原位点之间的关系,评估抗DNA抗体阻断生物素化抗DNA与固相DNA抗原相互作用的能力。对于每种测试的DNA,根据不同单克隆抗体的相对抑制活性,可以区分出两种DNA相互作用模式。这些结果表明,可以使用天然存在的DNA对抗DNA抗体进行表征,观察到的结合模式表明识别了独特的抗原位点,其中一些是离散且不重叠的。