In order to determine the possible use of uveal melanoma cell lines as
stimulators in immunotherapy, we evaluated the expression of the huma
n 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 tyrosi
nase genes and the HLA class I specificity were determined in five pri
mary and three metastatic uveal melanoma cell lines. Expression of the
examined genes was heterogeneous in the primary and metastatic cell l
ines. The cell lines OCM-1 and OMM-1 expressed MAGE-1, -2 and -3, wher
eas EOM-3, MEL202, 92-1 and OMM-3 were negative for these antigens. gp
100 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 microlymphocyto
toxicity assay. Since at least two melanoma-associated antigens can be
found in uveal melanoma cell lines, as well as the HLA class I molecu
les, these cell lines may be applicable as immunogens for specific imm
unotherapy against metastatic uveal melanoma. (C) 1998 Rapid Science L
td.