Bitter-Suermann D, Dierich M, König W, Hadding U
Immunology. 1972 Sep;23(3):267-81.
Antibody independent activation of the complement system starting with C3 can be achieved by means of a purified factor from cobra venom (VF), which interacts with a purified serum factor (SF). The latter is a normal constituent of guinea-pig and human serum (C3-proactivator). The interaction between VF and SF is Mg dependent and leads to the formation of a complex. Immunological analysis reveals that both VF- and SF-antigens are contained in the complex. The VF—SF complex activates enzymatically isolated C3, which in the presence of the subsequent components yields all effects of the normal complement sequence. Purified C5 is not affected by the complex. Its activation is mediated by activated C3. The VF—SF system represents a model for direct activation of C3 to C9 independent of antibody, C1, C4 and C2. An analogous pathway of alternate complement activation might be used by other substances, e.g. endotoxin, guinea-pig γ1-immune aggregates and zymosan. The corresponding serum factors are under investigation.
通过从眼镜蛇毒中提取的纯化因子(VF)可实现从C3开始的补体系统的抗体非依赖性激活,该因子与纯化的血清因子(SF)相互作用。后者是豚鼠和人血清的正常成分(C3前激活剂)。VF与SF之间的相互作用依赖于镁,并导致形成一种复合物。免疫分析表明,复合物中同时含有VF和SF抗原。VF-SF复合物可酶促激活分离出的C3,在后续成分存在的情况下,可产生正常补体序列的所有效应。纯化的C5不受该复合物影响。其激活由活化的C3介导。VF-SF系统代表了一种不依赖抗体、C1、C4和C2直接激活C3至C9的模型。其他物质,如内毒素、豚鼠γ1免疫聚集体和酵母聚糖,可能会使用类似的替代补体激活途径。相应的血清因子正在研究中。