ME1 is a monoclonal antibody which is generated by the use of a mesoth
elioma cell line (SPCIII). The antibody has a preferential reaction to
antigens on mesothelial and mesothelioma cells. In a prospective stud
y we determined the reactivity in frozen sections from malignant mesot
heliomas (two cases, positive controls), lung tumours (115 cases) and
other malignant tumours (23 cases). The two malignant mesotheliomas we
re immunoreactive in most of the tumour cells. The reaction was strong
, often with a diffuse staining of the cytoplasm and in some tumour ce
lls there was heavy staining of the cell membrane. Five adenocarcinoma
s of the lung (9%), one large cell carcinoma (10%) and 18 squamous cel
l carcinomas of the lung (41%) were positive (defined as tumours conta
ining more than 10% positive tumour cells with a strong reaction). The
same was true for seven out of 23 (30%) extrapulmonary malignancies.
The overall nosologic specificity of ME1 was 76%. Twenty out of the 26
ME1-positive lung tumours and six out of seven ME1-positive extrapulm
onary malignancies were also positive for one or more markers, which i
s considered characteristic of carcinomas. The six negative lung tumou
rs were squamous cells carcinomas and the negative extrapulmonary tumo
ur was a meningeoma; all of them with a morphology different to malign
ant mesothelioma. In conclusion, when frozen sections are available, M
E1 might be useful in the differential diagnosis of malignant tumours.
However, a positive reaction is not specific for malignant mesothelio
ma.