Hierholzer J C, Phillips D J, Humphrey D D, Coombs R A, Reimer C B
Arch Virol. 1984;80(1):1-10. doi: 10.1007/BF01315289.
An immunofluorometric assay (IFMA) has been evaluated as a screening assay to detect monoclonal antibodies to the group-specific antigen of the adenovirus hexon component. The antibodies were produced as mouse ascitic fluids from hybridoma cells generated from Balb/C mice immunized with purified adenovirus type 2 hexon component and crude adenovirus type 3 culture supernatants. The purified IgG fractions from all monoclonal ascitic fluids tested were identified as the IgG1 K mouse isotype. Antibody titers ranged from 102,400 to 204,800 by the IFMA, from 200 to 12,800 by indirect FA, and were generally nonreactive in counterelectrophoresis, complement fixation, hemagglutination-inhibition, serum neutralization, and immune electron microscopy titrations. The IFMA is a reliable method for quantitating low levels of specific antibody in large numbers of test samples, and is therefore ideal as a screening assay for monoclonal antibody in tissue culture fluids and in mouse ascitic fluids.
免疫荧光测定法(IFMA)已被评估为一种筛查测定法,用于检测针对腺病毒六邻体成分群特异性抗原的单克隆抗体。这些抗体是由用纯化的2型腺病毒六邻体成分和3型腺病毒粗培养上清液免疫的Balb/C小鼠产生的杂交瘤细胞分泌的小鼠腹水。所有测试的单克隆腹水纯化IgG组分均被鉴定为IgG1 K小鼠同种型。通过IFMA测定的抗体效价范围为102,400至204,800,通过间接荧光抗体法测定的效价范围为200至12,800,并且在对流电泳、补体结合、血凝抑制、血清中和及免疫电镜滴定中通常无反应性。IFMA是一种可靠的方法,可用于定量大量测试样品中的低水平特异性抗体,因此作为组织培养液和小鼠腹水中单克隆抗体的筛查测定法非常理想。