Luyten G P, van der Spek C W, Brand I, Sintnicolaas K, de Waard-Siebinga I, Jager M J, de Jong P T, Schrier P I, Luider T M
Department of Ophthalmology, Erasmus University Rotterdam, The Netherlands.
Melanoma Res. 1998 Feb;8(1):11-6. doi: 10.1097/00008390-199802000-00003.
In order to determine the possible use of uveal melanoma cell lines as stimulators in immunotherapy, we evaluated the expression of the human genes for MAGE-1, -2 and -3, gp100 and tyrosinase in uveal melanoma cell lines. mRNA expression of the MAGE-1, -2 and -3, gp100 and tyrosinase genes and the HLA class I specificity were determined in five primary and three metastatic uveal melanoma cell lines. Expression of the examined genes was heterogeneous in the primary and metastatic cell lines. The cell lines OCM-1 and OMM-1 expressed MAGE-1, -2 and -3, whereas EOM-3, MEL202, 92-1 and OMM-3 were negative for these antigens. gp100 was expressed in all cell lines, and tyrosinase in all but three (EOM-29, OMM-2 and OMM-3). Except for EOM-3, the HLA-A type of all the cell lines could be determined by complement-dependent microlymphocytotoxicity assay. Since at least two melanoma-associated antigens can be found in uveal melanoma cell lines, as well as the HLA class I molecules, these cell lines may be applicable as immunogens for specific immunotherapy against metastatic uveal melanoma.
为了确定葡萄膜黑色素瘤细胞系作为免疫治疗刺激剂的潜在用途,我们评估了葡萄膜黑色素瘤细胞系中人类MAGE-1、-2和-3、gp100及酪氨酸酶基因的表达情况。在五个原发性和三个转移性葡萄膜黑色素瘤细胞系中测定了MAGE-1、-2和-3、gp100及酪氨酸酶基因的mRNA表达以及HLA I类特异性。所检测基因的表达在原发性和转移性细胞系中是异质性的。细胞系OCM-1和OMM-1表达MAGE-1、-2和-3,而EOM-3、MEL202、92-1和OMM-3对这些抗原呈阴性。gp100在所有细胞系中均有表达,酪氨酸酶除三个细胞系(EOM-29、OMM-2和OMM-3)外均有表达。除EOM-3外,所有细胞系的HLA-A型均可通过补体依赖的微量淋巴细胞毒性试验确定。由于在葡萄膜黑色素瘤细胞系中可发现至少两种黑色素瘤相关抗原以及HLA I类分子,这些细胞系可能适用于作为针对转移性葡萄膜黑色素瘤的特异性免疫治疗的免疫原。