Shi L R, Eichelbauer D, Borchard F, Jürgens H, Göbel U, Schneider E M
Immunology Laboratory, Institute of Blood Coagulation and Transfusion Medicine, University of Düsseldorf, Germany.
Cancer Immunol Immunother. 1994 Mar;38(3):208-13. doi: 10.1007/BF01525643.
A selection of 16 monoclonal antibodies has been produced against a fresh Ewing's sarcoma (ES) tumor mixed with a permanent ES cell line. The majority of antibodies identify an 80-kDa molecule, which is not detected on healthy tissues except on certain cultured monocytes. One antibody recognizes the CD2 ligand MIC2 and 2 antibodies (numbers 13 and 16) define a higher-molecular-mass antigen. Antibody 16 is also expressed on mesenchymal fibroblasts of bone marrow or fetal origin. Tumor-specific antigen expression is potentially linked to the chromosome 22 abnormality described in Ewing's sarcoma, products altered expression in tumors with the chromosome 11/22 translocation has not been shown. The putative chimeric protein on chromosome 11 is apparently not expressed to a great extent, as tested by Northern blotting; however, the fusion protein initiated on chromosome 22 and ending on chromosome 11 is readily seen on Northern blots. The altered expression of a number of cellular genes in addition to a novel gene product(s) originating from translocation events were expected to be identified by monoclonal antibodies selected by their unique binding pattern to Ewing's sarcoma (ES) cells.
已制备出16种单克隆抗体,这些抗体针对的是与一种永久性尤文肉瘤(ES)细胞系混合的新鲜尤文肉瘤(ES)肿瘤。大多数抗体识别一种80 kDa的分子,除了某些培养的单核细胞外,在健康组织中未检测到该分子。一种抗体识别CD2配体MIC2,2种抗体(编号13和16)界定了一种分子量更高的抗原。抗体16也在骨髓或胎儿来源的间充质成纤维细胞上表达。肿瘤特异性抗原的表达可能与尤文肉瘤中描述的22号染色体异常有关,尚未证明在具有11/22号染色体易位的肿瘤中产物表达发生改变。如通过Northern印迹法检测,11号染色体上假定的嵌合蛋白显然没有大量表达;然而,在Northern印迹上很容易看到起始于22号染色体并终止于11号染色体的融合蛋白。除了源自易位事件的新型基因产物外,预计还能通过根据其与尤文肉瘤(ES)细胞独特结合模式选择的单克隆抗体识别许多细胞基因的表达改变。