Eisenbrey A B, Krebs T, Dunnette S, Gleich G J
J Immunol Methods. 1983 Mar 25;58(3):365-73. doi: 10.1016/0022-1759(83)90364-2.
Because the study of human IgE synthesis and regulation requires exquisitely sensitive and rapidly performed methods for assay of in vitro IgE production, we compared 4 methods for radiometric immunoassay (RIA) of human IgE: double antibody RIA (DARIA), ultrasensitive enzymatic RIA (USERIA), sensitive paper radioimmunosorbent test (SPRIST) and microtiter solid-phase RIA (MSPRIA). IgE protein was measured in serum samples and cord bloods. The USERIA and the MSPRIA consistently detected levels of IgE as low as 27-35 pg/ml. The DARIA and SPRIST were less sensitive. Comparison of the USERIA and the MSPRIA favored the latter because: (1) it is a more rapidly performed assay, (2) it involves fewer manipulations, and (3) it has less variability. We conclude that the MSPRIA for IgE is superior to the other methods both as a research tool for measuring minute quantities of IgE protein (as in tissue culture supernatants) and for measuring IgE in serum samples where concentrations fall below 1 ng/ml (0.42 IU/ml; 1 IU = 2.4 ng).
由于对人类IgE合成与调节的研究需要用于体外IgE产生检测的极其灵敏且能快速完成的方法,我们比较了4种用于人IgE放射免疫测定(RIA)的方法:双抗体RIA(DARIA)、超灵敏酶促RIA(USERIA)、灵敏纸放射免疫吸附试验(SPRIST)和微量滴定板固相RIA(MSPRIA)。在血清样本和脐带血中测量IgE蛋白。USERIA和MSPRIA始终能检测到低至27 - 35 pg/ml的IgE水平。DARIA和SPRIST的灵敏度较低。对USERIA和MSPRIA的比较表明后者更具优势,原因如下:(1)它是一种执行速度更快的检测方法;(2)它涉及的操作更少;(3)它的变异性更小。我们得出结论,用于IgE的MSPRIA无论是作为测量微量IgE蛋白(如在组织培养上清液中)的研究工具,还是用于测量血清样本中浓度低于1 ng/ml(0.42 IU/ml;1 IU = 2.4 ng)的IgE,都优于其他方法。