Poplack D G, Bonnard G D, Holiman B J, Blaese R M
Blood. 1976 Dec;48(6):809-16.
The lack of a simple, rapid, and quantitative test of the functional activity of the monocyte has hampered studies of the contribution of this cell type to host defense and human disease. This report describes an assay of antibody-dependent cellular cytotoxicity, which depends exclusively upon the monocyte as the effector cell and therefore provides a convenient test of monocyte function. In this system, mononuclear leukocytes (MNL) obtained by Ficoll-Hypaque separation of whole blood are cytotoxic for 51Cr-labeled human erythrocyte targets coated with anti-blood group antibody. Removal of phagocytic monocytes from the MNL by iron ingestion, followed by exposure to a magnetic field, completely abolishes all cytotoxic activity from the remaining MNL population. Similarly, in severely mono-cytopenic patients with aplastic anemia, cytotoxic effector activity is absent. In normals and less severely monocytopenic aplastic anemia patients, cytotoxicity correlates significantly (p less than 0.001) with monocyte number. Application of this monocyte-mediated antibody-dependent cellular cytotoxicity assay to the study of patients with the Wiskott-Aldrich syndrome has revealed defective monocyte cytotoxic activity in spite of normal monocyte numbers, suggesting that this test may be useful for the assessment of monocyte function in a variety of clinical situations.
缺乏一种简单、快速且能定量检测单核细胞功能活性的方法,这阻碍了对该细胞类型在宿主防御及人类疾病中所起作用的研究。本报告描述了一种抗体依赖性细胞毒性检测方法,该方法仅依赖单核细胞作为效应细胞,因此为单核细胞功能提供了一种便捷的检测手段。在这个系统中,通过Ficoll-Hypaque分离全血获得的单核白细胞(MNL)对包被有抗血型抗体的51Cr标记的人红细胞靶细胞具有细胞毒性。通过铁摄取从MNL中去除吞噬性单核细胞,然后暴露于磁场中,会完全消除剩余MNL群体的所有细胞毒性活性。同样,在严重单核细胞减少的再生障碍性贫血患者中,不存在细胞毒性效应活性。在正常人和单核细胞减少程度较轻的再生障碍性贫血患者中,细胞毒性与单核细胞数量显著相关(p小于0.001)。将这种单核细胞介导的抗体依赖性细胞毒性检测方法应用于Wiskott-Aldrich综合征患者的研究中,发现尽管单核细胞数量正常,但单核细胞的细胞毒性活性存在缺陷,这表明该检测方法可能有助于评估多种临床情况下的单核细胞功能。