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分泌人单克隆抗体的杂交瘤细胞上淋巴细胞表面标志物的表达

Lymphocyte surface marker expression on hybridomas secreting human monoclonal antibodies.

作者信息

Seifert M, Jahn S, Schwab J, Döcke W, Volk H D, von Baehr R

机构信息

Department of Medical Immunology, Medical School (Charité), Humboldt University of Berlin, Germany.

出版信息

Hum Antibodies Hybridomas. 1992 Apr;3(2):86-92.

PMID:1633269
Abstract

The expression of human leucocyte markers on the surface of hybridoma cell lines producing human monoclonal antibodies was studied using immunofluorescence analysis (FACS). We tested 36 different hybridoma cell lines from fusions of lymphocytes of different organs of fetal and adult organisms with the mouse myeloma line P3 X63 Ag8.653 or the mouse-human heteromyeloma line CB-F7 (IgM-, IgG-, and nonproducer) with a panel of 21 murine monoclonal antibodies against human differentiation and activation antigens. CD2, 3, 4, 5, 8, 10, 23, 25 antigen and major histocompatibility complex (MHC) class II determinants could not be detected on all hybridomas analyzed. The antigens CD22, 69, 71, and 72 were expressed on few of the hybridomas tested. The majority of the cell lines carried the surface markers CD19, 20, 40, 45 as well as the plasma cell markers CD38 and O/C11. The activation antigen 4F2 was expressed on all the cell lines tested. However, a direct connection between the expression of a lymphocyte marker and the capacity for Ig production (high and low producer; Ig isotype), the origin of the lymphocytes, and the fusion cell line used could not be detected.

摘要

利用免疫荧光分析(荧光激活细胞分选术)研究了产生人单克隆抗体的杂交瘤细胞系表面人白细胞标志物的表达情况。我们用一组21种针对人分化和激活抗原的鼠单克隆抗体,检测了来自胎儿和成年生物体不同器官淋巴细胞与小鼠骨髓瘤系P3 X63 Ag8.653或小鼠-人异种骨髓瘤系CB-F7(IgM-、IgG-和不产生抗体的细胞系)融合得到的36种不同杂交瘤细胞系。在所分析的所有杂交瘤细胞系中均未检测到CD2、3、4、5、8、10、23、25抗原以及主要组织相容性复合体(MHC)II类决定簇。抗原CD22、69、71和72仅在少数所检测的杂交瘤细胞系中表达。大多数细胞系携带表面标志物CD19、20、40、45以及浆细胞标志物CD38和O/C11。激活抗原4F2在所检测的所有细胞系中均有表达。然而,未检测到淋巴细胞标志物的表达与Ig产生能力(高产和低产;Ig同种型)、淋巴细胞来源以及所用融合细胞系之间存在直接联系。

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