Harmon M W, Phillips D J, Reimer C B, Kendal A P
J Clin Microbiol. 1986 Dec;24(6):913-6. doi: 10.1128/jcm.24.6.913-916.1986.
Mouse monoclonal antibodies specific for human immunoglobulin isotypes were investigated for use in an isotype-specific enzyme immunoassay for detection of antibody to influenza type A hemagglutinin (H1 and H3). The monoclonal antibody reagents were compared with isotype-specific, hyperimmune rabbit antisera from the National Institutes of Health. Endpoint titers for immunoglobulin G (IgG) obtained with the two reagents were within fourfold of each other 84% of the time (79 of 84) and within eightfold of each other 95% of the time (89 of 94). Regression analysis of the data gave a multiple correlation coefficient (r2) of 0.77 and a Spearman rank value of 0.83 (P less than 0.001). For IgA reagents, endpoint titers agreed within fourfold 77% of the time (88 of 114) and within eightfold 92% of the time (105 of 114). The r2 was 0.73, and Spearman rank was 0.83 (P less than 0.001). IgM antibody was detected in only 17 of 114 sera by either monoclonal or polyclonal reagents. Of these sera, 14 (82%) gave titers with the two reagents that were within fourfold of each other. A similar number of fourfold titer rises were detected with each reagent in paired sera showing hemagglutination inhibition titer rises. Monoclonal antibody reagents detected 27 IgA, 29 IgG, and 6 IgM rises, while polyclonal antisera detected 26 IgA, 31 IgG, and 7 IgM rises. These results show that monoclonal antibodies specific for human immunoglobulin isotypes are suitable as reagents for diagnostic assays. The advantages of monoclonal antibodies are their high degree of specificity and the ability to be standardized and produced in unlimited quantities. Moreover, the availability of immunoglobulin subclass- and allotype-specific monoclonal antibodies will enable a more detailed analysis of the antibody response to influenza as well as other infectious agents.
研究了针对人免疫球蛋白同种型的小鼠单克隆抗体,用于一种同种型特异性酶免疫测定,以检测抗甲型流感血凝素(H1和H3)的抗体。将单克隆抗体制剂与来自美国国立卫生研究院的同种型特异性超免疫兔抗血清进行了比较。用这两种试剂获得的免疫球蛋白G(IgG)的终点滴度在84%的时间内(84次中的79次)彼此相差四倍以内,在95%的时间内(94次中的89次)彼此相差八倍以内。对数据进行回归分析得到多重相关系数(r2)为0.77,Spearman秩值为0.83(P小于0.001)。对于IgA试剂,终点滴度在77%的时间内(114次中的88次)相差四倍以内,在92%的时间内(114次中的105次)相差八倍以内。r2为0.73,Spearman秩为0.83(P小于0.001)。在114份血清中,只有17份通过单克隆或多克隆试剂检测到IgM抗体。在这些血清中,14份(82%)用两种试剂测得的滴度彼此相差四倍以内。在显示血凝抑制滴度升高的配对血清中,每种试剂检测到的四倍滴度升高数量相似。单克隆抗体制剂检测到27份IgA升高、29份IgG升高和6份IgM升高,而多克隆抗血清检测到26份IgA升高、31份IgG升高和7份IgM升高。这些结果表明,针对人免疫球蛋白同种型的单克隆抗体适合作为诊断测定的试剂。单克隆抗体的优点是其高度特异性以及能够标准化并大量生产。此外,免疫球蛋白亚类和同种异型特异性单克隆抗体的可用性将能够对流感以及其他感染因子的抗体反应进行更详细的分析。