Veenstra H, Close P, Dowdle E B
MRC Human Cell Biology Research Unit, University of Cape Town.
S Afr Med J. 1987 Dec 5;72(11):794-6.
A monoclonal antibody-secreting hybridoma cell line, VCD-1, was derived from the fusion of murine myeloma cells with splenocytes from a BALB/c mouse that had been immunised with chronic B-lymphocytic leukaemia cells. The cells came from a patient who had developed the leukaemia approximately 10 years after a course of radiotherapy for nodular sclerosing Hodgkin's disease. The antibody bound to a 30,000-dalton protein that was present in normal and malignant B cells, in monocytes, neutrophils, and interdigitating reticulum cells, and in malignant cells present in Hodgkin's disease lymph nodes. The reactive epitope was not accessible to antibody in viable intact cells; binding to peripheral blood cells could only be seen if the cells were fixed. The antibody recognises a determinant that probably resides on the alpha-chain of HLA class II molecules.
一种分泌单克隆抗体的杂交瘤细胞系VCD - 1,是由小鼠骨髓瘤细胞与来自一只用慢性B淋巴细胞白血病细胞免疫的BALB/c小鼠的脾细胞融合而成。这些细胞来自一名患者,该患者在接受结节硬化型霍奇金病放射治疗约10年后患上了白血病。该抗体与一种30000道尔顿的蛋白质结合,这种蛋白质存在于正常和恶性B细胞、单核细胞、中性粒细胞和交错突网状细胞以及霍奇金病淋巴结中的恶性细胞中。在活的完整细胞中,反应表位不能被抗体识别;只有在细胞固定后才能看到与外周血细胞的结合。该抗体识别一个可能位于HLA II类分子α链上的决定簇。