Steward M W, Collins M J, Stanley C, Devey M E
Br J Exp Pathol. 1981 Dec;62(6):614-22.
Daily injection of human serum albumin into mice genetically selected to produce low-affinity antibody to protein antigens resulted in a more severe antigen-antibody-complex-induced glomerulonephritis than in mice producing high-affinity antibody. The low-affinity mice had higher levels of circulating antigen-antibody complexes, greater impairment of renal function and reduced reticuloendothelial clearance of 125I-PVP compared to high-affinity mice. Electron microscopy of glomeruli revealed the presence of subepithelial electron-dense deposits in low-affinity mice and predominantly subendothelial-mesangial deposits in high-affinity mice which corresponded to the predominantly capillary staining in low-affinity mice and mesangial staining in high-affinity mice by immunofluorescence. Auto-radiography of electron-microscopy sections demonstrated the presence of antigen in the electron-dense deposits, indicating that these deposits indeed contained antigen-antigen complexes.
每天给经过基因筛选产生低亲和力蛋白质抗原抗体的小鼠注射人血清白蛋白,会导致比产生高亲和力抗体的小鼠更严重的抗原-抗体复合物诱导的肾小球肾炎。与高亲和力小鼠相比,低亲和力小鼠循环中的抗原-抗体复合物水平更高,肾功能损害更大,125I-PVP的网状内皮清除率降低。肾小球的电子显微镜检查显示,低亲和力小鼠存在上皮下电子致密沉积物,高亲和力小鼠主要是内皮下-系膜沉积物,这与免疫荧光显示的低亲和力小鼠主要为毛细血管染色、高亲和力小鼠为系膜染色相对应。电子显微镜切片的放射自显影显示电子致密沉积物中存在抗原,表明这些沉积物确实含有抗原-抗体复合物。