The MAGE gene family, encoding tumor-rejection antigens recognized by
cytotoxic T lymphocytes, is frequently expressed in human solid cancer
s. However, its expression in leukemia has not been well studied. We h
ave investigated MAGE gene expression at the mRNA level in human leuke
mia. The MAGE gene family was expressed in 17 of 34 (50%) examples of
T cell leukemia (12/21 patients' peripheral blood mononuclear cells an
d 5/13 cell lines), in 7 of 16 (44%) cases of B cell leukemia (1/8 and
6/8 respectively), but in none of 23 myelomonocytic leukemia cases (0
/16 and 0/7), as evaluated by the primers common to the MAGE-1, -3, -4
(-4a and/or -4b), and -6 genes and the semi-quantificative reverse tr
anscription/polymerase chain reaction method. None of a panel of norma
l lymphoid cells expressed the MAGE gene family. As revealed by the pr
imers specific for each of the MAGE genes, the MAGE-1, -2, -3, -4 or -
6 gene was expressed in 8, 8, 6, 2, or 6 respectively out of 23 types
of leukemia cell lines. Expression of the MAGE-1 protein in both the c
ell lines and patients' cells was confirmed by immunoblot analysis wit
h the polyclonal antibody to recombinant MAGE-1 protein. Cellular MAGE
-4 protein in the cell lines was measured by an enzyme-linked immunoso
rbent assay with the polyclonal and monoclonal antibodies to recombina
nt MAGE-4b protein. In summary, the MAGE gene family was found to be e
xpressed in the substantial proportion of T cell leukemias, but in no
case of myelomonocytic leukemia. Antigens coded by the MAGE gene famil
y could be important molecules for understanding specific immunity aga
inst lymphocytic leukemia.