Palmer D K, Morse H G, Jones C
Eleanor Roosevelt Institute for Cancer Research, Denver, CO 80206.
Mol Immunol. 1987 Aug;24(8):865-9. doi: 10.1016/0161-5890(87)90189-1.
Five monoclonal antibodies which indirectly agglutinate human rbc were isolated and designated 2D8, 4E12, 4H10, 5A8, and 5H5. Expression of the antigen defined by 2D8 was 100% concordant with the presence of human chromosome 19 in a panel of human-Chinese hamster somatic cell hybrids. Secondary clones isolated from antigen positive hybrids exposed to antibody 2D8 and complement were shown to have lost both the cell surface antigen and chromosome 19. Small terminal deletions of 19p were observed in the karyotypes of two antigen negative clones that continued to express human GPI. All five monoclonal antibodies and the previously isolated F10 labelled the surface of parental cells and did not label the surface of deletion mutants, and the five monoclonal antibodies produced in this study inhibited the binding of F10 to the human rbc surface. Therefore, all must recognize the MSK20 cell surface antigen which was defined previously by antibody F10. Chimpanzee cells bind 5A8 and 5H5, orangutan cells bind 4E12, and neither bind 2D8 and 4H10. Therefore, the monoclonal antibodies produced in this study must recognize at least three distinct epitopes of the MSK20 cell surface antigen which are expressed on the human rbc.
分离出五种间接凝集人红细胞的单克隆抗体,分别命名为2D8、4E12、4H10、5A8和5H5。在一组人-中国仓鼠体细胞杂种中,由2D8定义的抗原表达与人类19号染色体的存在100%一致。从暴露于抗体2D8和补体的抗原阳性杂种中分离出的二次克隆显示已失去细胞表面抗原和19号染色体。在两个继续表达人GPI的抗原阴性克隆的核型中观察到19p的小末端缺失。所有五种单克隆抗体和先前分离的F10均标记亲代细胞表面,而不标记缺失突变体的表面,并且本研究中产生的五种单克隆抗体抑制F10与人红细胞表面的结合。因此,所有这些抗体必定识别先前由抗体F10定义的MSK20细胞表面抗原。黑猩猩细胞结合5A8和5H5,猩猩细胞结合4E12,两者均不结合2D8和4H10。因此,本研究中产生的单克隆抗体必定识别MSK20细胞表面抗原的至少三个不同表位,这些表位在人红细胞上表达。