Homburger H A, McCarthy R, Deodhar S
Section of Clinical Immunology, Mayo Clinic, Rochester, MN 55905.
Arch Pathol Lab Med. 1989 Jun;113(6):667-72.
In 1986, the College of American Pathologists introduced an interlaboratory proficiency testing program for clinical laboratories that perform flow cytometry. Specimens consisting of fresh human lymphocytes isolated from blood or tissue or neoplastic cells grown in culture were mailed to participants by overnight mail. Results of analyses for cell surface antigens on lymphocytes and for cellular DNA content were reported to the College of American Pathologists Computer Center and the summary data were mailed to participants. The results obtained to date indicate no reagent- or instrument-related biases for measurements of cell surface antigens or for cellular DNA content. Interlaboratory variability in enumerating lymphocytes of a given subset varies inversely with the percentage of such cells in each specimen. In our experience, it is feasible and practical to conduct an interlaboratory proficiency survey in clinical flow cytometry.
1986年,美国病理学家学会为开展流式细胞术检测的临床实验室推出了一项实验室间能力验证计划。由从血液或组织中分离出的新鲜人类淋巴细胞或培养的肿瘤细胞组成的样本通过隔夜快递寄给参与者。淋巴细胞表面抗原分析结果和细胞DNA含量分析结果被报告给美国病理学家学会计算机中心,汇总数据则寄给参与者。迄今获得的结果表明,在细胞表面抗原测量或细胞DNA含量测量方面不存在与试剂或仪器相关的偏差。给定亚群淋巴细胞计数的实验室间变异性与每个样本中此类细胞的百分比成反比。根据我们的经验,在临床流式细胞术中开展实验室间能力验证调查是可行且实际的。