The human MAGE gene family encodes products that can be recognized by autol
ogous cytotoxic T cells. Because MACE genes are silent in most normal tissu
es except testis but are activated in a variety of neoplastic lesions, MAGE
antigens represent ideal targets for immunotherapy. Current knowledge of M
AGE gene expression is based primarily on mRNA typing and relatively little
is known about MAGE protein expression. Monoclonal antibody (MAb) 57B, ori
ginally thought to be specific for MAGE-3, but now known to be reactive wit
h other MAGE components, was used in the present study to analyze MACE expr
ession in a panel of normal and malignant tissues. In tests with a wide ran
ge of normal tissues, only spermatogenic cells of testis were reactive with
57B, In tumor tissues, significant immunoreactivity was observed in malign
ant melanomas and carcinomas of the lung, head and neck as well as urinary
bladder. No 57B reactivity was seen with colorectal, prostatic or renal cel
l carcinomas. Lipo- and myosarcomas, as well as malignant fibrous histiocyt
oma (MFH), were negative, but synovial sarcomas showed intense immunoreacti
vity, A subset of seminomas was also strongly reactive with 57B, Tumor spec
imens showed great variability in the number of tumor cells showing 57B rea
ctivity, with some tumors showing only small isolated clusters of positive
cells to other tumors with uniform staining throughout the tumor. Int. J, C
ancer 85:460-465, 2000, (C) 2000 Wiley-Liss, Inc.