Gfl. Hofbauer et al., TYROSINASE IMMUNOREACTIVITY IN FORMALIN-FIXED, PARAFFIN-EMBEDDED PRIMARY AND METASTATIC MELANOMA - FREQUENCY AND DISTRIBUTION, Journal of cutaneous pathology, 25(4), 1998, pp. 204-209
Monoclonal antibody T311 specifically detects tyrosinase protein expre
ssion. Tyrosinase-derived peptides are recognized by CD8+ T-cells and
applied in immunotherapy. We examined formalin-fixed paraffin-embedded
tissue of 50 melanoma (primary n=31, metastatic n=19) and 41 control
cases (junctional, dermal, compound, Spitz, Reed, balloon-cell nevi) b
y immunochemistry using the alkaline phosphatase-anti-alkaline phospha
tase method after antigen retrieval. Staining with mAb T311 showed a s
ensitivity of 94% for melanoma with a very high specificity for melano
cytic cells. Immunopositivity (94% of melanomas overall) correlated in
versely with clinical stage: clinical stage I and stage II showed 100%
, stage III and stage IV 86% immunoreactivity each. Staining changed f
rom an exclusively homogeneous pattern in early stages to a more heter
ogeneous pattern in later stages. Melanocytic control tissue like nevi
of different subtypes all showed weak to moderate, homogeneous immuno
reactivity with polarity towards the epidermis. RT-PCR ELISA analysis
of short-term melanoma cell cultures displaced mRNA expression in only
half of the originally immunopositive tumors only suggesting rapid mR
NA expression loss in culture, mAb T311 allows detection of melanoma-a
ssociated tyrosinase protein expression and thus profiling of melanoma
s using routine archival tissue suited for immunotherapy approaches in
volving tyrosinase derived epitopes. (C) Munksgaard 1998.