Richardson M D, Warnock D W
J Immunol Methods. 1984 Jan 20;66(1):119-32. doi: 10.1016/0022-1759(84)90255-2.
Four commercial antigen extracts of Aspergillus fumigatus were evaluated for use in a rapid enzyme-linked immunosorbent assay (ELISA) for anti-A. fumigatus IgG. Initial binding of both somatic and culture filtrate preparations to a polyvinyl chloride solid phase was concentration dependent and increased with incubation time. Antigen binding to the solid phase was reproducible. Binding of A. fumigatus precipitin-positive serum to bound antigen was rapid. All four A. fumigatus antigens demonstrated similar dose-response curves when tested against pooled sera containing a high titre of A. fumigatus antibodies. Detectable activity in precipitin test-negative sera decreased rapidly with dilution. All the antigen preparations were found to be suitable for ELISA procedures and permit the rapid determination of IgG antibodies to A. fumigatus.
对四种烟曲霉商业抗原提取物进行了评估,以用于抗烟曲霉IgG的快速酶联免疫吸附测定(ELISA)。菌体和培养滤液制剂与聚氯乙烯固相的初始结合呈浓度依赖性,并随孵育时间增加。抗原与固相的结合具有可重复性。烟曲霉沉淀素阳性血清与结合抗原的结合迅速。当用含有高滴度烟曲霉抗体的混合血清进行检测时,所有四种烟曲霉抗原均显示出相似的剂量反应曲线。沉淀素试验阴性血清中的可检测活性随稀释迅速降低。发现所有抗原制剂均适用于ELISA程序,并可快速测定抗烟曲霉IgG抗体。