HLA-DR antigens on differentiating human mammary gland epithelium and breast tumours
Language English Country Great Britain, England Media print
Document type Journal Article
PubMed
3435699
PubMed Central
PMC2002386
DOI
10.1038/bjc.1987.278
Knihovny.cz E-resources
- MeSH
- Cell Differentiation MeSH
- Epithelium immunology MeSH
- HLA-D Antigens analysis MeSH
- HLA-DR Antigens analysis MeSH
- Lactation immunology MeSH
- Leukocytes immunology MeSH
- Humans MeSH
- Mitosis MeSH
- Antibodies, Monoclonal MeSH
- Cell Transformation, Neoplastic immunology MeSH
- Breast Neoplasms immunology MeSH
- Breast immunology MeSH
- Pregnancy MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Pregnancy MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- HLA-D Antigens MeSH
- HLA-DR Antigens MeSH
- Antibodies, Monoclonal MeSH
The staining pattern of a monoclonal antibody directed to the monomorphic determinant of HLA-DR antigens was examined on sections of human mammary gland tissues at various stages of differentiation as well as on 50 benign and 72 malignant breast lesions. Normal resting breast epithelium lacked HLA-DR, whereas late-pregnant and lactating epithelia expressed high levels of HLA-DR antigens, followed by a decline in the post-weaning regression period. Most benign breast lesions revealed heterogeneous staining ranging from very few up to 20-25% positive epithelial Greater variability was observed among carcinomas, where a small group (approximately 7%) of cases showing 40-95% positive tumour cells was found, in addition to negative tumours and those with the minority of HLA-DR expressing carcinoma cells. The density of the leukocytic infiltrate was higher in carcinomas than in either normal breast tissue or benign lesions, the HLA-DR phenotype of the mononuclear infiltrating cells lacking any obvious correlation with the HLA-DR status of the epithelial component. Immunoblotting analyses of whole-tissue lysates separated by SDS-PAGE confirmed the immunohistochemical data and demonstrated the reactivity with only one protein band predicted for HLA-DR alpha-chain. The combination of immunohistochemistry and autoradiography on sections of human reduction mammoplasty organoids cultured in collagen gels and labelled with tritiated thymidine revealed a lack of HLA-DR expression on proliferating breast epithelial cells suggesting factors other than cell kinetics must be responsible for induction of HLA-DR antigens seen in pregnant and lactating breast epithelium and some tumours.
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