Welch T R, Forristal J, Beischel L
J Lab Clin Med. 1986 Jun;107(6):529-33.
A relationship was found between the sums of the component proteins of the classical pathway C3 convertase (C2 and C4) and their regulators (C4bp and 1) in 184 normal controls. The relationship was maintained in most patients with low levels of individual components resulting from congenital deficiency and urinary losses, as well as in most cord sera. On the other hand, classical pathway activation in membranoproliferative glomerulonephritis type I, systemic lupus erythematosus, hereditary angioneurotic edema, and bacteremia resulted in loss of this relationship. Patients with alternative pathway-mediated complement activation (membranoproliferative glomerulonephritis type II) had a normal relationship between the classical component and regulatory proteins. In situations in which classical pathway activation is suspected, simultaneous examination of C4, C2, C4bp, and I may be helpful.
在184名正常对照者中,发现经典途径C3转化酶的组成蛋白(C2和C4)与其调节蛋白(C4bp和I)的总和之间存在关联。在大多数因先天性缺陷和尿液丢失导致个别成分水平较低的患者以及大多数脐带血清中,这种关联得以维持。另一方面,I型膜增生性肾小球肾炎、系统性红斑狼疮、遗传性血管性水肿和菌血症中的经典途径激活导致这种关联丧失。由替代途径介导补体激活的患者(II型膜增生性肾小球肾炎),经典成分与调节蛋白之间的关系正常。在怀疑有经典途径激活的情况下,同时检测C4、C2、C4bp和I可能会有帮助。