Connell P A, Seehra M S, Leslie R G, Reeves W G
Eur J Immunol. 1980 Dec;10(12):966-8. doi: 10.1002/eji.1830101214.
The chemiluminescence (CL) response of guinea pig peritoneal macrophages to immune precipitates and soluble immune complexes has been investigated. The rapid burst of intense light emission observed in response to both stimuli, was inhibited by superoxide dismutase (SOD). With soluble immune complexes, this was followed by prolonged CL of lower intensity susceptible to both SOD and catalase inhibition. The magnitude of the CL response was directly related to seize the size of the soluble complexes reacting with the macrophages. These findings suggest that circulating, as distinct from deposited immune complexes, may play a role in the pathogenesis of complex-mediated diseases.
对豚鼠腹膜巨噬细胞对免疫沉淀物和可溶性免疫复合物的化学发光(CL)反应进行了研究。观察到对两种刺激的快速强烈发光爆发都被超氧化物歧化酶(SOD)抑制。对于可溶性免疫复合物,随后是强度较低的长时间CL,且易受SOD和过氧化氢酶抑制。CL反应的强度与与巨噬细胞反应的可溶性复合物的大小直接相关。这些发现表明,与沉积的免疫复合物不同,循环免疫复合物可能在复杂介导疾病的发病机制中起作用。