Haas G G, D'Cruz O J
Department of Obstetrics and Gynecology, University of Oklahoma Health Sciences Center, Oklahoma City.
Am J Reprod Immunol. 1989 Jun;20(2):37-43. doi: 10.1111/j.1600-0897.1989.tb00637.x.
An indirect inhibition assay was devised to quantitate the amount of immunoglobulin molecules on the surface of human sperm. Sperm-associated IgG was used to inhibit competitively 125I-labeled polyclonal anti-human IgG from binding to human IgG affixed to microtissue culture plate wells. Standard curves for the assay were derived by substituting soluble IgG in the supernatant of the tissue culture wells for sperm-associated IgG. The intraassay coefficient of variation was 6.7%; the interassay coefficient of variation was 5.6-21% depending upon the IgG antisperm antibody-positive plasma sample assayed. The assay technique was highly correlated (r = 0.99) with the number of antibody-bound sperm added to the supernatant. When different sperm donors were utilized as an antigen source, the coefficient of variation was 15.6% for positive plasmas and 19.3% for negative plasmas. The indirect inhibition assay showed a strong correlation (r = 0.91) with a previously described radiolabeled antiglobulin assay for sperm-associated IgG.
设计了一种间接抑制试验来定量人精子表面免疫球蛋白分子的数量。精子相关IgG用于竞争性抑制125I标记的多克隆抗人IgG与固定在微孔组织培养板孔中的人IgG结合。该试验的标准曲线是通过用组织培养孔上清液中的可溶性IgG替代精子相关IgG得出的。试验内变异系数为6.7%;试验间变异系数为5.6 - 21%,具体取决于所检测的IgG抗精子抗体阳性血浆样本。该试验技术与添加到上清液中的抗体结合精子数量高度相关(r = 0.99)。当使用不同的精子供体作为抗原来源时,阳性血浆的变异系数为15.6%,阴性血浆的变异系数为19.3%。间接抑制试验与先前描述的用于检测精子相关IgG的放射性标记抗球蛋白试验显示出强相关性(r = 0.91)。