Ross J, Dickerson T, Perkins H A
Tissue Antigens. 1975 Sep;6(3):129-36. doi: 10.1111/j.1399-0039.1975.tb00626.x.
Two techniques capable of increasing the sensitivity of the lymphocytotoxic crossmatch test were compared for sensitivity and practically using the fluorochromasia modification of the cytotoxicity test. Prolonging the incubation period after addition of complement in the standard test resulted in further positive reactions. Modification of the test by addition of antiglobulin reagent increased the reactivity more than prolonged incubation of the standard test. The fluorochromasia adaptation of the antiglobulin test had sensitivity equivalent to the original antiglobulin method. The antiglobulin technique had a number of disadvantages, and neither the prolonged incubation nor the antiglobulin procedure meet the requirements of a busy histocompatibility testing service in view of the time consumed for the first and the complexity of the second.
为了比较两种能够提高淋巴细胞毒性交叉配型试验敏感性的技术的敏感性和实用性,采用细胞毒性试验的荧光染色法进行了研究。在标准试验中添加补体后延长孵育期,会导致更多阳性反应。添加抗球蛋白试剂对试验进行改良,其反应性的提高幅度大于标准试验延长孵育期的情况。抗球蛋白试验的荧光染色改良法的敏感性与原抗球蛋白法相当。抗球蛋白技术存在一些缺点,考虑到第一种方法耗时且第二种方法复杂,延长孵育期和抗球蛋白程序均不符合繁忙的组织相容性检测服务的要求。