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T cells but not NK cells are associated with a favourable outcome for resected colorectal liver metastases

BACKGROUND: The adaptive immune response to colorectal cancer is important for survival. Less is understood about the role of innate lymphocytes, such as Natural Killer (NK) cells, which are abundant in human liver. METHODS: Samples of fresh liver (n = 21) and tumour (n = 11) tissue were obtained fr...

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Autores principales: Pugh, Siân A, Harrison, Rebecca J, Primrose, John N, Khakoo, Salim I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995621/
https://www.ncbi.nlm.nih.gov/pubmed/24625075
http://dx.doi.org/10.1186/1471-2407-14-180
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author Pugh, Siân A
Harrison, Rebecca J
Primrose, John N
Khakoo, Salim I
author_facet Pugh, Siân A
Harrison, Rebecca J
Primrose, John N
Khakoo, Salim I
author_sort Pugh, Siân A
collection PubMed
description BACKGROUND: The adaptive immune response to colorectal cancer is important for survival. Less is understood about the role of innate lymphocytes, such as Natural Killer (NK) cells, which are abundant in human liver. METHODS: Samples of fresh liver (n = 21) and tumour (n = 11) tissue were obtained from patients undergoing surgical resection of colorectal liver metastases. Flow cytometry was used to analyse the presence and phenotype of NK cells, as compared to T cells, in the tumour and liver tissue. Results were correlated with survival. RESULTS: NK cells were poorly recruited to the tumours (distant liver tissue 38.3%, peritumoural liver 34.2%, tumour 12.9%, p = 0.0068). Intrahepatic and intratumoural NK cells were KIR (killer immunoglobulin-like receptor)(lo)NKG2A(hi) whereas circulating NK cells were KIR(hi)NKG2A(lo). By contrast T cells represented 65.7% of the tumour infiltrating lymphocytes. Overall survival was 43% at 5 years, with the 5-year survival for individuals with a T cell rich infiltrate being 60% (95% CI 17-93%) and for those with a low T cell infiltrate being 0% (95% CI 0-48%). Conversely individuals with higher levels of NK cells in the tumour had an inferior outcome, although there were insufficient numbers to reach significance (median survivals: NK(Hi) 1.63 years vs NK(Lo) 3.92 years). CONCLUSIONS: T cells, but not NK cells, are preferentially recruited to colorectal liver metastases. NK cells within colorectal metastases have an intrahepatic and potentially tolerogenic, rather than a peripheral, phenotype. Similar to primary tumours, the magnitude of the T cell infiltrate in colorectal metastases is positively associated with survival.
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spelling pubmed-39956212014-04-23 T cells but not NK cells are associated with a favourable outcome for resected colorectal liver metastases Pugh, Siân A Harrison, Rebecca J Primrose, John N Khakoo, Salim I BMC Cancer Research Article BACKGROUND: The adaptive immune response to colorectal cancer is important for survival. Less is understood about the role of innate lymphocytes, such as Natural Killer (NK) cells, which are abundant in human liver. METHODS: Samples of fresh liver (n = 21) and tumour (n = 11) tissue were obtained from patients undergoing surgical resection of colorectal liver metastases. Flow cytometry was used to analyse the presence and phenotype of NK cells, as compared to T cells, in the tumour and liver tissue. Results were correlated with survival. RESULTS: NK cells were poorly recruited to the tumours (distant liver tissue 38.3%, peritumoural liver 34.2%, tumour 12.9%, p = 0.0068). Intrahepatic and intratumoural NK cells were KIR (killer immunoglobulin-like receptor)(lo)NKG2A(hi) whereas circulating NK cells were KIR(hi)NKG2A(lo). By contrast T cells represented 65.7% of the tumour infiltrating lymphocytes. Overall survival was 43% at 5 years, with the 5-year survival for individuals with a T cell rich infiltrate being 60% (95% CI 17-93%) and for those with a low T cell infiltrate being 0% (95% CI 0-48%). Conversely individuals with higher levels of NK cells in the tumour had an inferior outcome, although there were insufficient numbers to reach significance (median survivals: NK(Hi) 1.63 years vs NK(Lo) 3.92 years). CONCLUSIONS: T cells, but not NK cells, are preferentially recruited to colorectal liver metastases. NK cells within colorectal metastases have an intrahepatic and potentially tolerogenic, rather than a peripheral, phenotype. Similar to primary tumours, the magnitude of the T cell infiltrate in colorectal metastases is positively associated with survival. BioMed Central 2014-03-13 /pmc/articles/PMC3995621/ /pubmed/24625075 http://dx.doi.org/10.1186/1471-2407-14-180 Text en Copyright © 2014 Pugh et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Pugh, Siân A
Harrison, Rebecca J
Primrose, John N
Khakoo, Salim I
T cells but not NK cells are associated with a favourable outcome for resected colorectal liver metastases
title T cells but not NK cells are associated with a favourable outcome for resected colorectal liver metastases
title_full T cells but not NK cells are associated with a favourable outcome for resected colorectal liver metastases
title_fullStr T cells but not NK cells are associated with a favourable outcome for resected colorectal liver metastases
title_full_unstemmed T cells but not NK cells are associated with a favourable outcome for resected colorectal liver metastases
title_short T cells but not NK cells are associated with a favourable outcome for resected colorectal liver metastases
title_sort t cells but not nk cells are associated with a favourable outcome for resected colorectal liver metastases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995621/
https://www.ncbi.nlm.nih.gov/pubmed/24625075
http://dx.doi.org/10.1186/1471-2407-14-180
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