Bishara A, Brautbar C, Marbach A, Bonavida B, Nelken D
J Immunol Methods. 1983 Aug 26;62(2):265-71. doi: 10.1016/0022-1759(83)90254-5.
HLA-A and -B antigens were detected on fresh and dried peripheral blood lymphocytes by an enzyme-linked immunosorbent assay. Intact cells fixed to plates with glutaraldehyde were used as antigen and anti-HLA alloantisera as a source of antibodies. Determination of HLA antigens by the ELISA technique was comparable with the complement-dependent cytotoxicity test. The relative stability of HLA antigens as shown in this report and the extensive polymorphism of the HLA system make the ELISA technique a promising tool for the analysis of HLA antigens on non-living cells including, for example, medicolegal investigation of blood stains.
采用酶联免疫吸附测定法检测新鲜和干燥外周血淋巴细胞上的HLA - A和 - B抗原。用戊二醛固定在平板上的完整细胞作为抗原,抗HLA同种抗血清作为抗体来源。通过酶联免疫吸附测定技术测定HLA抗原与补体依赖细胞毒性试验相当。本报告所示的HLA抗原的相对稳定性以及HLA系统的广泛多态性使得酶联免疫吸附测定技术成为分析非活细胞上HLA抗原的一种有前景的工具,例如用于血迹的法医学调查。