Koethe S M, Casper J T, Rodey G E
Clin Exp Immunol. 1976 Jan;23(1):56-60.
The low molecular weight cobra venom factor (CoVF) was used to activate the terminal sequence of the alternative complement pathway in thirty-one sera from patients with sickle cell disease (SCD). The SCD sera were compared with normal sera as a source of the alternative complement pathway factors C3 proactivator (C3PA) and C3PA convertase. These factors are required for formation of the enzymatically active CoVF-C3PA complex which is capable of cleaving C3 and thus initiating generation of the cytolytic C5b-9 complex. CoVF cofactor activity was significantly less than normal in SCD sera as measured in an indirect lysis assay, indicating reduced C3PA or C3PA convertase activity in these sera. Qualitative (immunoelectrophoresis) and quantitative (radial immunodiffusion) measurement of C3PA showed, however, that this protein is normal or elevated in SCD sera. Taken together, the reduced CoVF cofactor activity and normal or elevated C3PA in SCD sera suggests that sera from patients with sickle cell disease have reduced C3PA convertase activity.
低分子量眼镜蛇毒因子(CoVF)用于激活31例镰状细胞病(SCD)患者血清中替代补体途径的终末序列。将SCD患者血清与正常血清进行比较,后者作为替代补体途径因子C3前活化剂(C3PA)和C3PA转化酶的来源。这些因子是形成具有酶活性的CoVF - C3PA复合物所必需的,该复合物能够裂解C3,从而启动溶细胞性C5b - 9复合物的生成。在间接溶血试验中测得,SCD患者血清中的CoVF辅因子活性显著低于正常水平,表明这些血清中C3PA或C3PA转化酶活性降低。然而,对C3PA进行定性(免疫电泳)和定量(放射免疫扩散)检测发现,SCD患者血清中该蛋白含量正常或升高。综合来看,SCD患者血清中CoVF辅因子活性降低以及C3PA正常或升高,提示镰状细胞病患者血清中C3PA转化酶活性降低。