Tedesco F, Rottini G, Patriarca P
J Immunol. 1981 Nov;127(5):1910-5.
The effect of complement (C) components on the intracellular killing of E. coli 0111:B4 by human PMN was studied. Various intermediate bacteria were prepared by opsonizing IgM-coated 0111:B4 with yeast cell-treated human serum (BAC1-3), a C6-deficient human serum (BAC1-5), a C8-deficient human serum (BAC1-7), a C8-deficient human serum, and with partially purified C8 (BAC1-8). All these bacterial preparations were phagocytosed by human PMN, but only BAC1-8 and, to a lesser extent, BAC1-5 were killed. Similar results were obtained when the 400 x G postnuclear supernatant (PNS) of PMN homogenate was used instead of intact leukocytes. The C9 nature of the killing factor in the PMN homogenate was ruled out by its inability to lyse EAC1-8 and by the finding that the killing of BAC1-8 by the PMN factor was not inhibited by the antiserum against human C9. The anti-C5 and anti-C8 antisera were unable to inhibit the killing by the PNS of BAC1-5 and BAC1-8, respectively, suggesting that bound C5 and C8 do not provide a binding site for the killing factor.
研究了补体(C)成分对人中性粒细胞(PMN)胞内杀灭大肠杆菌0111:B4的影响。通过用酵母细胞处理的人血清(BAC1 - 3)、C6缺陷型人血清(BAC1 - 5)、C8缺陷型人血清(BAC1 - 7)、C8缺陷型人血清以及部分纯化的C8(BAC1 - 8)调理包被IgM的0111:B4,制备了各种中间细菌。所有这些细菌制剂均被人PMN吞噬,但只有BAC1 - 8以及程度稍轻的BAC1 - 5被杀死。当使用PMN匀浆的400×G核后上清液(PNS)代替完整白细胞时,得到了类似的结果。PMN匀浆中杀伤因子的C9性质被排除,因为它不能裂解EAC1 - 8,并且发现PMN因子对BAC1 - 8的杀伤不受抗人C9抗血清的抑制。抗C5和抗C