Abstract |
The expression of HLA-A,B,C antigens and lymphocyte function-associated antigen 3 in human colorectal adenomas and adenocarcinomas was studied by immunohistochemistry. None of 10 adenomas and only 1 of 30 carcinomas had lost expression of all HLA-A,B,C molecules. On the other hand, focal loss of an HLA-B product was seen in 2 of the adenomas, and complete losses of tumor cell HLA-A2 (in 7 of 13 cases), HLA-Bw4 (in 4 of 13 cases), and HLA-A3 (in 1 of 6 cases) were seen in the carcinomas. No complete losses of HLA-A1 (in 6 cases) or HLA-Bw6 (in 22 cases) occurred in the carcinomas. In addition, 1 of 20 adenocarcinomas totally lacked lymphocyte function-associated antigen 3. Because a loss of tumor cell HLA-A,B,C antigen or lymphocyte function-associated antigen 3 could be selected for through an advantage in escape from cytotoxic T-lymphocyte attack, our results suggest that immunoselection may be a more important mechanism in tumor progression than has previously been assumed.
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Authors | M E Smith, S G Marsh, J G Bodmer, K Gelsthorpe, W F Bodmer |
Journal | Proceedings of the National Academy of Sciences of the United States of America
(Proc Natl Acad Sci U S A)
Vol. 86
Issue 14
Pg. 5557-61
(Jul 1989)
ISSN: 0027-8424 [Print] United States |
PMID | 2473473
(Publication Type: Journal Article)
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Chemical References |
- Antigens, Surface
- CD58 Antigens
- HLA-A Antigens
- HLA-B Antigens
- HLA-C Antigens
- Membrane Glycoproteins
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Topics |
- Adenocarcinoma
(genetics, immunology, pathology)
- Adenoma
(genetics, immunology, pathology)
- Alleles
- Antigens, Surface
(genetics)
- CD58 Antigens
- Colonic Neoplasms
(genetics, immunology, pathology)
- Genes, MHC Class II
- HLA-A Antigens
(analysis, genetics)
- HLA-B Antigens
(analysis, genetics)
- HLA-C Antigens
(analysis, genetics)
- Humans
- Immunoenzyme Techniques
- Membrane Glycoproteins
(genetics)
- Tumor Cells, Cultured
(immunology)
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