Intraepithelial CD8+ T-cell-count becomes a prognostic factor after a longer follow-up period in human colorectal carcinoma: possible association with suppression ... View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2004-10-19

AUTHORS

T Chiba, H Ohtani, T Mizoi, Y Naito, E Sato, H Nagura, A Ohuchi, K Ohuchi, K Shiiba, Y Kurokawa, S Satomi

ABSTRACT

T-cell infiltration into human cancer tissues can be a manifestation of host immune responses to cancer cells. The present study was undertaken to explore the clinicopathological significance of intraepithelial CD8+ T cells using 371 consecutively sampled human colorectal carcinomas. By univariate analysis, we noted that the survival curves by intraepithelial CD8+ T cells became separated only after 1 to 2 years postoperation. Multivariate analyses revealed that the beneficial effect of this factor becomes significant only after a longer (more than 2 year), but not after a shorter (less than 2 year) follow-up period. Furthermore, the number of intraepithelial CD8+ T cells was significantly higher in patients alive for more than 5 years than in patients who either died of cancer after a curative operation or patients who underwent a noncurative operation. Patients' cancer-specific death long after a curative operation is thought to be caused by the growth of micrometastases in other organs or near the primary sites. The effects of intraepithelial CD8+ T cells, therefore, may be mediated by suppression of micrometastasis, rather than suppression of growth in the primary tumour. In conclusion, our data support a hypothesis on the presence of systemic immunosurveillance against micrometastasis of cancer cells. More... »

PAGES

1711-1717

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/sj.bjc.6602201

DOI

http://dx.doi.org/10.1038/sj.bjc.6602201

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1011870228

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/15494715


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