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Temporal changes in immune cell composition and cytokines in response to chemoradiation in rectal cancer

We measured systemic changes in the immune response in 92 patients receiving preoperative chemoradiation therapy (CRT) and subsequent surgery for rectal cancer. The peripheral blood was sampled five times from the onset of CRT until surgery. Lymphocytes decreased continuously during CRT but increase...

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Autores principales: Lee, Yong Joon, Lee, Sat Byol, Beak, Suk Kyung, Han, Yoon Dae, Cho, Min Soo, Hur, Hyuk, Lee, Kang Young, Kim, Nam Kyu, Min, Byung Soh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5953940/
https://www.ncbi.nlm.nih.gov/pubmed/29765096
http://dx.doi.org/10.1038/s41598-018-25970-z
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author Lee, Yong Joon
Lee, Sat Byol
Beak, Suk Kyung
Han, Yoon Dae
Cho, Min Soo
Hur, Hyuk
Lee, Kang Young
Kim, Nam Kyu
Min, Byung Soh
author_facet Lee, Yong Joon
Lee, Sat Byol
Beak, Suk Kyung
Han, Yoon Dae
Cho, Min Soo
Hur, Hyuk
Lee, Kang Young
Kim, Nam Kyu
Min, Byung Soh
author_sort Lee, Yong Joon
collection PubMed
description We measured systemic changes in the immune response in 92 patients receiving preoperative chemoradiation therapy (CRT) and subsequent surgery for rectal cancer. The peripheral blood was sampled five times from the onset of CRT until surgery. Lymphocytes decreased continuously during CRT but increased after CRT. The increased lymphocyte population was predominantly CD8+ T lymphocytes, which accounted for a significantly larger proportion in patients without residual lymph node metastasis than in those with residual lymph node metastasis. Neutrophils and monocytes decreased during the initial two weeks of CRT but were maintained or increased afterwards. Neutrophil and monocyte counts were significantly lower in patients with a pCR (pathologic complete response) than in those without a pCR two weeks after CRT began but not at the initiation of CRT. All cytokines showed dramatic changes one month after the termination of CRT. Cytokines related to the antitumour immune response increased, and those related to tumour progression decreased. The predictive value of cytokines was not clear. In short, we observed that immune components in peripheral blood are affected by CRT and show dynamic changes over time. We identified biomarker candidates to predict the pathologic response in the future.
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spelling pubmed-59539402018-05-21 Temporal changes in immune cell composition and cytokines in response to chemoradiation in rectal cancer Lee, Yong Joon Lee, Sat Byol Beak, Suk Kyung Han, Yoon Dae Cho, Min Soo Hur, Hyuk Lee, Kang Young Kim, Nam Kyu Min, Byung Soh Sci Rep Article We measured systemic changes in the immune response in 92 patients receiving preoperative chemoradiation therapy (CRT) and subsequent surgery for rectal cancer. The peripheral blood was sampled five times from the onset of CRT until surgery. Lymphocytes decreased continuously during CRT but increased after CRT. The increased lymphocyte population was predominantly CD8+ T lymphocytes, which accounted for a significantly larger proportion in patients without residual lymph node metastasis than in those with residual lymph node metastasis. Neutrophils and monocytes decreased during the initial two weeks of CRT but were maintained or increased afterwards. Neutrophil and monocyte counts were significantly lower in patients with a pCR (pathologic complete response) than in those without a pCR two weeks after CRT began but not at the initiation of CRT. All cytokines showed dramatic changes one month after the termination of CRT. Cytokines related to the antitumour immune response increased, and those related to tumour progression decreased. The predictive value of cytokines was not clear. In short, we observed that immune components in peripheral blood are affected by CRT and show dynamic changes over time. We identified biomarker candidates to predict the pathologic response in the future. Nature Publishing Group UK 2018-05-15 /pmc/articles/PMC5953940/ /pubmed/29765096 http://dx.doi.org/10.1038/s41598-018-25970-z Text en © The Author(s) 2018 Open Access 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 http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lee, Yong Joon
Lee, Sat Byol
Beak, Suk Kyung
Han, Yoon Dae
Cho, Min Soo
Hur, Hyuk
Lee, Kang Young
Kim, Nam Kyu
Min, Byung Soh
Temporal changes in immune cell composition and cytokines in response to chemoradiation in rectal cancer
title Temporal changes in immune cell composition and cytokines in response to chemoradiation in rectal cancer
title_full Temporal changes in immune cell composition and cytokines in response to chemoradiation in rectal cancer
title_fullStr Temporal changes in immune cell composition and cytokines in response to chemoradiation in rectal cancer
title_full_unstemmed Temporal changes in immune cell composition and cytokines in response to chemoradiation in rectal cancer
title_short Temporal changes in immune cell composition and cytokines in response to chemoradiation in rectal cancer
title_sort temporal changes in immune cell composition and cytokines in response to chemoradiation in rectal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5953940/
https://www.ncbi.nlm.nih.gov/pubmed/29765096
http://dx.doi.org/10.1038/s41598-018-25970-z
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