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Functional Alteration of Natural Killer Cells and Cytotoxic T Lymphocytes upon Asbestos Exposure and in Malignant Mesothelioma Patients

Malignant mesothelioma is caused by exposure to asbestos, which is known to have carcinogenic effects. However, the development of mesothelioma takes a long period and results from a low or intermediate dose of exposure. These findings have motivated us to investigate the immunological effects of as...

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Autores principales: Nishimura, Yasumitsu, Kumagai-Takei, Naoko, Matsuzaki, Hidenori, Lee, Suni, Maeda, Megumi, Kishimoto, Takumi, Fukuoka, Kazuya, Nakano, Takashi, Otsuki, Takemi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486484/
https://www.ncbi.nlm.nih.gov/pubmed/26161391
http://dx.doi.org/10.1155/2015/238431
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author Nishimura, Yasumitsu
Kumagai-Takei, Naoko
Matsuzaki, Hidenori
Lee, Suni
Maeda, Megumi
Kishimoto, Takumi
Fukuoka, Kazuya
Nakano, Takashi
Otsuki, Takemi
author_facet Nishimura, Yasumitsu
Kumagai-Takei, Naoko
Matsuzaki, Hidenori
Lee, Suni
Maeda, Megumi
Kishimoto, Takumi
Fukuoka, Kazuya
Nakano, Takashi
Otsuki, Takemi
author_sort Nishimura, Yasumitsu
collection PubMed
description Malignant mesothelioma is caused by exposure to asbestos, which is known to have carcinogenic effects. However, the development of mesothelioma takes a long period and results from a low or intermediate dose of exposure. These findings have motivated us to investigate the immunological effects of asbestos exposure and analyze immune functions of patients with mesothelioma and pleural plaque, a sign of exposure to asbestos. Here, we review our knowledge concerning natural killer (NK) cells and cytotoxic T lymphocytes (CTL). NK cells showed impaired cytotoxicity with altered expression of activating receptors upon exposure to asbestos, while induction of granzyme(+) cells in CD8(+) lymphocytes was suppressed by asbestos exposure. It is interesting that a decrease in NKp46, a representative activating receptor, is common between NK cells in PBMC culture with asbestos and those of mesothelioma patients. Moreover, it was observed that CD8(+) lymphocytes may be stimulated by some kind of “nonself” cells in plaque-positive individuals and in mesothelioma patients, whereas CTL in mesothelioma is impaired by poststimulation maintenance of cytotoxicity. These findings suggest that analysis of immunological parameters might contribute to the evaluation of health conditions of asbestos-exposed individuals and to a greater understanding of the pathology of malignant mesothelioma.
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spelling pubmed-44864842015-07-09 Functional Alteration of Natural Killer Cells and Cytotoxic T Lymphocytes upon Asbestos Exposure and in Malignant Mesothelioma Patients Nishimura, Yasumitsu Kumagai-Takei, Naoko Matsuzaki, Hidenori Lee, Suni Maeda, Megumi Kishimoto, Takumi Fukuoka, Kazuya Nakano, Takashi Otsuki, Takemi Biomed Res Int Review Article Malignant mesothelioma is caused by exposure to asbestos, which is known to have carcinogenic effects. However, the development of mesothelioma takes a long period and results from a low or intermediate dose of exposure. These findings have motivated us to investigate the immunological effects of asbestos exposure and analyze immune functions of patients with mesothelioma and pleural plaque, a sign of exposure to asbestos. Here, we review our knowledge concerning natural killer (NK) cells and cytotoxic T lymphocytes (CTL). NK cells showed impaired cytotoxicity with altered expression of activating receptors upon exposure to asbestos, while induction of granzyme(+) cells in CD8(+) lymphocytes was suppressed by asbestos exposure. It is interesting that a decrease in NKp46, a representative activating receptor, is common between NK cells in PBMC culture with asbestos and those of mesothelioma patients. Moreover, it was observed that CD8(+) lymphocytes may be stimulated by some kind of “nonself” cells in plaque-positive individuals and in mesothelioma patients, whereas CTL in mesothelioma is impaired by poststimulation maintenance of cytotoxicity. These findings suggest that analysis of immunological parameters might contribute to the evaluation of health conditions of asbestos-exposed individuals and to a greater understanding of the pathology of malignant mesothelioma. Hindawi Publishing Corporation 2015 2015-06-16 /pmc/articles/PMC4486484/ /pubmed/26161391 http://dx.doi.org/10.1155/2015/238431 Text en Copyright © 2015 Yasumitsu Nishimura et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Nishimura, Yasumitsu
Kumagai-Takei, Naoko
Matsuzaki, Hidenori
Lee, Suni
Maeda, Megumi
Kishimoto, Takumi
Fukuoka, Kazuya
Nakano, Takashi
Otsuki, Takemi
Functional Alteration of Natural Killer Cells and Cytotoxic T Lymphocytes upon Asbestos Exposure and in Malignant Mesothelioma Patients
title Functional Alteration of Natural Killer Cells and Cytotoxic T Lymphocytes upon Asbestos Exposure and in Malignant Mesothelioma Patients
title_full Functional Alteration of Natural Killer Cells and Cytotoxic T Lymphocytes upon Asbestos Exposure and in Malignant Mesothelioma Patients
title_fullStr Functional Alteration of Natural Killer Cells and Cytotoxic T Lymphocytes upon Asbestos Exposure and in Malignant Mesothelioma Patients
title_full_unstemmed Functional Alteration of Natural Killer Cells and Cytotoxic T Lymphocytes upon Asbestos Exposure and in Malignant Mesothelioma Patients
title_short Functional Alteration of Natural Killer Cells and Cytotoxic T Lymphocytes upon Asbestos Exposure and in Malignant Mesothelioma Patients
title_sort functional alteration of natural killer cells and cytotoxic t lymphocytes upon asbestos exposure and in malignant mesothelioma patients
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486484/
https://www.ncbi.nlm.nih.gov/pubmed/26161391
http://dx.doi.org/10.1155/2015/238431
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