Williams D, Esquenazi V, Cirocco R, Jensen J A
J Immunol. 1976 Feb;116(2):554-61.
Neutrophils (PMN) migrated in vitro chemotactically along concentration gradients of heterologous and homologous leukocytotoxic, complement-active sera. The heterologous systems consisted of normal, non-immune nurse shark or dog serum and human PMN; the homologous systems consisted of human or dog immune sera and human or dog PMN, respectively. Chemotaxis was induced 1) by fresh cytotoxic sera, 2) by complement alone if the cytotoxic antibodies were with the responding cells or if the cells were passively sensitized with the antibodies, and 3) by individual and combined complement components if the corresponding intermediate PMN-antibody-complement component complexes were the migrating cells. These observations represent a new mechanism of immune chemotaxis: the chemotactic stimulation is a direct consequence of a gradient-controlled immune reaction occuring at and involving the surface of the chemoattracted cell. This mechanism is distinctly different from that which depends on chemotactic factors produced or released independent of and at a distance from the responding cells.
中性粒细胞(PMN)在体外沿异源和同源白细胞毒性、补体活性血清的浓度梯度进行趋化迁移。异源系统由正常的、非免疫的护士鲨或狗血清与人PMN组成;同源系统分别由人或狗的免疫血清与人或狗的PMN组成。趋化作用由以下因素诱导:1)新鲜的细胞毒性血清;2)如果细胞毒性抗体与反应细胞在一起,或者细胞被抗体被动致敏,则单独由补体诱导;3)如果相应的中间PMN-抗体-补体成分复合物是迁移细胞,则由单个和组合的补体成分诱导。这些观察结果代表了免疫趋化的一种新机制:趋化刺激是在趋化吸引细胞表面发生并涉及该表面的梯度控制免疫反应的直接结果。这种机制与依赖于独立于反应细胞产生或释放且与反应细胞有一定距离的趋化因子的机制明显不同。