Gfl. Hofbauer et al., MAGE-3 IMMUNOREACTIVITY IN FORMALIN-FIXED, PARAFFIN-EMBEDDED PRIMARY AND METASTATIC MELANOMA - FREQUENCY AND DISTRIBUTION, The American journal of pathology, 151(6), 1997, pp. 1549-1553
Monoclonal antibody 57B specifically detects MAGE-3 gene protein expre
ssion, MAGE-derived peptides are recognized by CD8(+) T cells and appl
ied in immunotherapy, We examined formalin-fixed, paraffin-embedded ti
ssue of 61 melanoma (primary, n = 40; metastatic, n = 21) and 46 contr
ol cases (junctional, dermal, compound, Spitz, Reed, and balloon-cell
nevi) by immunohistochemistry using the alkaline phosphatase anti-alka
line phosphatase method after antigen retrieval, Immunoreactivity was
rated positive at 20 positive cells per tumor or more, Staining patter
n was homogeneous, scattered, or focal, AU. control samples and intern
al controls were immunonegative. Staining with monoclonal antibody 57B
showed a specificity of 100% with a sensitivity of 44%, Immunopositiv
ity (overall, 44% of melanomas) increased along with tumor, node, and
metastasis stage; pT1 showed 15%, pT2 22%, pT3a 29%, pT3b 45%, pT4 100
%, pTxN1 60%, and pTxNxM1a 63% of samples positive, The staining patte
rn was homogeneous on pT1 to pT3a tumors, homogeneous or focal in pT3b
and pT4a, and homogeneous, focal, or scattered in pTxN1 and pTxNxM1a,
The frequency of immunopositivity relates well to data on mRNA expres
sion using reverse transcriptase polymerase chain reaction in a subgro
up analyzed by both methods, Monoclonal antibody 57B can be used to al
low profiling of melanomas using routine archival tissue, when conside
ring immunotherapeutic approaches involving MAGE-3-derived epitopes.