Freedman J, Massey A
Transfusion. 1981 Jan-Feb;21(1):32-7. doi: 10.1046/j.1537-2995.1981.21181127480.x.
Anti-C3d sera were raised to different C3d antigens or to the same C3d antigen by different methods. Although identical by immunoprecipitation studies, the various anti-C3d sera showed differences in specificities against bound C3d antigen. Such differences were observed wih red blood cells coated with C3d in vivo and in vitro. Antisera made to the C3d-KAF antigen detected fewer molecules/cell on C3d-tryp cells than did antisera made to the C3d-tryp antigen. The converse was true for C3d-KAF cells. "Saturation" experiments indicated that different anti-C3d detected different "subpopulations" of bound C3d. C3d bound to red blood cells in vivo was, in at least one case, detectable by some anti-C3d sera but not by others. Such differences in anti-C3d specificity may be important in determining the optimal characteristics of anti-C3d antiglobulin serum for routine laboratory use.
通过不同方法制备了针对不同C3d抗原或相同C3d抗原的抗C3d血清。尽管通过免疫沉淀研究显示相同,但各种抗C3d血清在针对结合的C3d抗原的特异性上存在差异。在体内和体外涂有C3d的红细胞上观察到了这种差异。针对C3d-KAF抗原制备的抗血清在C3d-胰蛋白酶处理的细胞上检测到的分子/细胞比针对C3d-胰蛋白酶抗原制备的抗血清少。对于C3d-KAF细胞,情况则相反。“饱和”实验表明,不同的抗C3d检测到结合的C3d的不同“亚群”。在至少一种情况下,体内与红细胞结合的C3d可被某些抗C3d血清检测到,但不能被其他血清检测到。抗C3d特异性的这种差异对于确定常规实验室使用的抗C3d抗球蛋白血清的最佳特性可能很重要。