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Concurrent infiltration by CD8(+) T cells and CD4(+) T cells is a favourable prognostic factor in non-small-cell lung carcinoma

The purpose of this study was to clarify the relationship between the number of tumour-infiltrating T lymphocytes and the clinicopathological features and clinical outcome in patients with non-small-cell lung cancer (NSCLC). Tissue specimens from 109 patients who underwent surgical resection for NSC...

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Autores principales: Hiraoka, K, Miyamoto, M, Cho, Y, Suzuoki, M, Oshikiri, T, Nakakubo, Y, Itoh, T, Ohbuchi, T, Kondo, S, Katoh, H
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361103/
https://www.ncbi.nlm.nih.gov/pubmed/16421594
http://dx.doi.org/10.1038/sj.bjc.6602934
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author Hiraoka, K
Miyamoto, M
Cho, Y
Suzuoki, M
Oshikiri, T
Nakakubo, Y
Itoh, T
Ohbuchi, T
Kondo, S
Katoh, H
author_facet Hiraoka, K
Miyamoto, M
Cho, Y
Suzuoki, M
Oshikiri, T
Nakakubo, Y
Itoh, T
Ohbuchi, T
Kondo, S
Katoh, H
author_sort Hiraoka, K
collection PubMed
description The purpose of this study was to clarify the relationship between the number of tumour-infiltrating T lymphocytes and the clinicopathological features and clinical outcome in patients with non-small-cell lung cancer (NSCLC). Tissue specimens from 109 patients who underwent surgical resection for NSCLC were immunohistochemically analysed for CD4 and CD8 expression. Patients were classified into two groups according to whether their tumours exhibited a ‘high’ or ‘low’ level of CD8(+) or CD4(+) lymphocyte infiltration. Although the level of infiltration by CD8(+) T cells alone had no prognostic significance, the survival rate for patients with both ‘high’ CD8(+) and ‘high’ CD4(+) T-cell infiltration was significantly higher than that for the other groups (log-rank test, P=0.006). Multivariate analysis indicated that concomitant high CD8(+) and high CD4(+) T-cell infiltration was an independent favourable prognostic factor (P=0.0092). In conclusion, the presence of high levels of both CD8(+) T cells and CD4(+) T cells is a significant indicator of a better prognosis for patients with NSCLC, and cooperation between these cell populations may allow a significantly more potent antitumour response than either population alone.
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spelling pubmed-23611032009-09-10 Concurrent infiltration by CD8(+) T cells and CD4(+) T cells is a favourable prognostic factor in non-small-cell lung carcinoma Hiraoka, K Miyamoto, M Cho, Y Suzuoki, M Oshikiri, T Nakakubo, Y Itoh, T Ohbuchi, T Kondo, S Katoh, H Br J Cancer Molecular Diagnostics The purpose of this study was to clarify the relationship between the number of tumour-infiltrating T lymphocytes and the clinicopathological features and clinical outcome in patients with non-small-cell lung cancer (NSCLC). Tissue specimens from 109 patients who underwent surgical resection for NSCLC were immunohistochemically analysed for CD4 and CD8 expression. Patients were classified into two groups according to whether their tumours exhibited a ‘high’ or ‘low’ level of CD8(+) or CD4(+) lymphocyte infiltration. Although the level of infiltration by CD8(+) T cells alone had no prognostic significance, the survival rate for patients with both ‘high’ CD8(+) and ‘high’ CD4(+) T-cell infiltration was significantly higher than that for the other groups (log-rank test, P=0.006). Multivariate analysis indicated that concomitant high CD8(+) and high CD4(+) T-cell infiltration was an independent favourable prognostic factor (P=0.0092). In conclusion, the presence of high levels of both CD8(+) T cells and CD4(+) T cells is a significant indicator of a better prognosis for patients with NSCLC, and cooperation between these cell populations may allow a significantly more potent antitumour response than either population alone. Nature Publishing Group 2006-01-30 2006-01-17 /pmc/articles/PMC2361103/ /pubmed/16421594 http://dx.doi.org/10.1038/sj.bjc.6602934 Text en Copyright © 2006 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Hiraoka, K
Miyamoto, M
Cho, Y
Suzuoki, M
Oshikiri, T
Nakakubo, Y
Itoh, T
Ohbuchi, T
Kondo, S
Katoh, H
Concurrent infiltration by CD8(+) T cells and CD4(+) T cells is a favourable prognostic factor in non-small-cell lung carcinoma
title Concurrent infiltration by CD8(+) T cells and CD4(+) T cells is a favourable prognostic factor in non-small-cell lung carcinoma
title_full Concurrent infiltration by CD8(+) T cells and CD4(+) T cells is a favourable prognostic factor in non-small-cell lung carcinoma
title_fullStr Concurrent infiltration by CD8(+) T cells and CD4(+) T cells is a favourable prognostic factor in non-small-cell lung carcinoma
title_full_unstemmed Concurrent infiltration by CD8(+) T cells and CD4(+) T cells is a favourable prognostic factor in non-small-cell lung carcinoma
title_short Concurrent infiltration by CD8(+) T cells and CD4(+) T cells is a favourable prognostic factor in non-small-cell lung carcinoma
title_sort concurrent infiltration by cd8(+) t cells and cd4(+) t cells is a favourable prognostic factor in non-small-cell lung carcinoma
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361103/
https://www.ncbi.nlm.nih.gov/pubmed/16421594
http://dx.doi.org/10.1038/sj.bjc.6602934
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