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Regulatory T-cell density and cytotoxic T lymphocyte density are associated with complete response to neoadjuvant paclitaxel and carboplatin chemoradiotherapy in gastric cancer

Regulatory T-cell density and cytotoxic T lymphocyte density are crucial in regulating antitumor immune responses. Tumor infiltration has marked therapeutic effects in gastric carcinoma, and there is evidence that chemoradiotherapy (CRT) exhibits an immune-mediated component. In the present study, t...

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Autores principales: Huang, Di, Yang, Yongjiang, Zhang, Shuai, Su, Zhuobin, Peng, Tao, Wang, Xiaoyuan, Zhao, Yifeng, Li, Shuguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176141/
https://www.ncbi.nlm.nih.gov/pubmed/30344657
http://dx.doi.org/10.3892/etm.2018.6684
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author Huang, Di
Yang, Yongjiang
Zhang, Shuai
Su, Zhuobin
Peng, Tao
Wang, Xiaoyuan
Zhao, Yifeng
Li, Shuguang
author_facet Huang, Di
Yang, Yongjiang
Zhang, Shuai
Su, Zhuobin
Peng, Tao
Wang, Xiaoyuan
Zhao, Yifeng
Li, Shuguang
author_sort Huang, Di
collection PubMed
description Regulatory T-cell density and cytotoxic T lymphocyte density are crucial in regulating antitumor immune responses. Tumor infiltration has marked therapeutic effects in gastric carcinoma, and there is evidence that chemoradiotherapy (CRT) exhibits an immune-mediated component. In the present study, the density of CD4(+) and CD8(+) cells were evaluated in post-CRT surgical samples from 68 patients with gastric cancer using immunohistochemistry. The associations between T-cell density, cytotoxic T lymphocyte density and clinical survival rate were also analyzed. Cytotoxic T lymphocyte density was associated with gastric carcinoma regression grade and regulatory T-cell density was also associated with gastric carcinoma regression grade. Of the patients who had a pathologic complete response, 84 and 76% were found to have a high CD3(+) and CD4(+) cell density, which was significantly different to patients who had a low CD3(+) and CD4(+) cell density. High cytotoxic T lymphocyte density was also associated with improved survival rates of patients with gastric cancer. In conclusion, these outcomes indicated that regulatory T-cell density and cytotoxic T lymphocyte density in the tumor microenvironment were associated with the response to neoadjuvant CRT and may represent a therapeutic target for gastric cancer.
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spelling pubmed-61761412018-10-21 Regulatory T-cell density and cytotoxic T lymphocyte density are associated with complete response to neoadjuvant paclitaxel and carboplatin chemoradiotherapy in gastric cancer Huang, Di Yang, Yongjiang Zhang, Shuai Su, Zhuobin Peng, Tao Wang, Xiaoyuan Zhao, Yifeng Li, Shuguang Exp Ther Med Articles Regulatory T-cell density and cytotoxic T lymphocyte density are crucial in regulating antitumor immune responses. Tumor infiltration has marked therapeutic effects in gastric carcinoma, and there is evidence that chemoradiotherapy (CRT) exhibits an immune-mediated component. In the present study, the density of CD4(+) and CD8(+) cells were evaluated in post-CRT surgical samples from 68 patients with gastric cancer using immunohistochemistry. The associations between T-cell density, cytotoxic T lymphocyte density and clinical survival rate were also analyzed. Cytotoxic T lymphocyte density was associated with gastric carcinoma regression grade and regulatory T-cell density was also associated with gastric carcinoma regression grade. Of the patients who had a pathologic complete response, 84 and 76% were found to have a high CD3(+) and CD4(+) cell density, which was significantly different to patients who had a low CD3(+) and CD4(+) cell density. High cytotoxic T lymphocyte density was also associated with improved survival rates of patients with gastric cancer. In conclusion, these outcomes indicated that regulatory T-cell density and cytotoxic T lymphocyte density in the tumor microenvironment were associated with the response to neoadjuvant CRT and may represent a therapeutic target for gastric cancer. D.A. Spandidos 2018-11 2018-09-03 /pmc/articles/PMC6176141/ /pubmed/30344657 http://dx.doi.org/10.3892/etm.2018.6684 Text en Copyright: © Huang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Huang, Di
Yang, Yongjiang
Zhang, Shuai
Su, Zhuobin
Peng, Tao
Wang, Xiaoyuan
Zhao, Yifeng
Li, Shuguang
Regulatory T-cell density and cytotoxic T lymphocyte density are associated with complete response to neoadjuvant paclitaxel and carboplatin chemoradiotherapy in gastric cancer
title Regulatory T-cell density and cytotoxic T lymphocyte density are associated with complete response to neoadjuvant paclitaxel and carboplatin chemoradiotherapy in gastric cancer
title_full Regulatory T-cell density and cytotoxic T lymphocyte density are associated with complete response to neoadjuvant paclitaxel and carboplatin chemoradiotherapy in gastric cancer
title_fullStr Regulatory T-cell density and cytotoxic T lymphocyte density are associated with complete response to neoadjuvant paclitaxel and carboplatin chemoradiotherapy in gastric cancer
title_full_unstemmed Regulatory T-cell density and cytotoxic T lymphocyte density are associated with complete response to neoadjuvant paclitaxel and carboplatin chemoradiotherapy in gastric cancer
title_short Regulatory T-cell density and cytotoxic T lymphocyte density are associated with complete response to neoadjuvant paclitaxel and carboplatin chemoradiotherapy in gastric cancer
title_sort regulatory t-cell density and cytotoxic t lymphocyte density are associated with complete response to neoadjuvant paclitaxel and carboplatin chemoradiotherapy in gastric cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176141/
https://www.ncbi.nlm.nih.gov/pubmed/30344657
http://dx.doi.org/10.3892/etm.2018.6684
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