Summary MHC class I antigens are intimately involved in intercellular communication, and recognition by cytotoxic T cells. Thus tumour cells that fail to express them may be at a growth or metastatic advantage. A series of ten colorectal and ten breast carcinomas, and their respective lymph node metastases, were examined immunohistologically using monoclonal antibodies (mAb) against both monomorphic and A2 polymorphic determinants, and beta-2-microglobulin (beta 2m). Four (Benacerraf, 1981;Linsk & Goodenow, 1986;Schwartz, 1982). The class I MHC molecule consists of three alpha regimes, covalently linked to beta-2-microglobulin (beta 2m), which are encoded by separate genes, and linked prior to expression at the cell membrane (Ploegh et al., 1981;Arce-Gomez, 1978 (Eisenbach et al., 1983;1985). Studies on the expression of human MHC class I antigens in primary vs metastatic tumour are limited; for example malignant melanoma, digestive tract, and laryngeal tumours (Ruiz-Cabello et al., 1989;Esteban et al., 1989). In these studies, both increased and decreased expression of monomorphic determinants of HLA class I was observed in the metastases compared with their primaries. In the present study we have used mAbs to evaluate a series of human primary colon and breast carcinomas, and their lymph node metastases, for the expression of monomorphic and polymorphic HLA class I determinants. Normal colon mucosa and, where possible, colon adenomas and liver metastases were included in the study. Many of the primary tumours at both sites showed reduced staining for monomorphic and polymorphic HLA class I determinants; metastases showed both greater and lesser degrees of loss of HLA expression when compared with their primary.
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