Blumberg N, Masel D, Stoler M
Blood. 1986 Jan;67(1):200-2.
Estimates of the number of IgG molecules bound to normal platelets have ranged from several hundred to several tens of thousands. The lower estimates were generated from direct binding assays and stoichiometric assumptions. The higher values derive from competitive binding assays, in which platelet-associated IgG (PAIgG) is calculated from a standard curve using soluble IgG standards. Using a kinetic-ELISA (enzyme-linked immunosorbent assay) antiglobulin assay, we measured normal platelet IgG to be 21,200 +/- 9,400 molecules per platelet when a competitive assay and soluble IgG standards were used. Direct measurement of bound antiglobulin by kinetic-ELISA and stoichiometric assumptions yielded a measurement of 259 +/- 117 IgG molecules per platelet. Soluble IgG and PAIgG are not comparable in their ability to bind anti-IgG. Disparities in estimates of normal PAIgG are probably due to methodological differences. The estimate most likely to be correct is several hundred IgG or less per normal platelet.
与正常血小板结合的IgG分子数量估计值在几百到数万之间。较低的估计值来自直接结合试验和化学计量假设。较高的值来自竞争性结合试验,其中血小板相关IgG(PAIgG)是根据使用可溶性IgG标准品的标准曲线计算得出的。使用动力学酶联免疫吸附测定(ELISA)抗球蛋白试验,当使用竞争性试验和可溶性IgG标准品时,我们测得正常血小板IgG为每血小板21,200±9,400个分子。通过动力学ELISA直接测量结合的抗球蛋白并结合化学计量假设,得出每血小板259±117个IgG分子的测量值。可溶性IgG和PAIgG结合抗IgG的能力不可比。正常PAIgG估计值的差异可能是由于方法学差异。最可能正确的估计是每个正常血小板有几百个或更少的IgG。