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Analysis of immune status after iodine-125 permanent brachytherapy in prostate cancer
BACKGROUND: Permanent prostate brachytherapy (PPB) is an effective treatment choice for low and intermediate risk prostate cancer (PCa). However, the impact of PPB on tumor immune status is still poorly understood. This study aimed to assess the immune status in PCa patients before and at different...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438076/ https://www.ncbi.nlm.nih.gov/pubmed/28546760 http://dx.doi.org/10.2147/OTT.S137491 |
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author | Du, E Wang, Lin Li, Chang-ying Zhang, Chang-wen Qu, Yan-chun Liu, Ran-lu Xu, Yong Yang, Kuo Zhang, Zhi-hong |
author_facet | Du, E Wang, Lin Li, Chang-ying Zhang, Chang-wen Qu, Yan-chun Liu, Ran-lu Xu, Yong Yang, Kuo Zhang, Zhi-hong |
author_sort | Du, E |
collection | PubMed |
description | BACKGROUND: Permanent prostate brachytherapy (PPB) is an effective treatment choice for low and intermediate risk prostate cancer (PCa). However, the impact of PPB on tumor immune status is still poorly understood. This study aimed to assess the immune status in PCa patients before and at different time points after PPB (1, 3, 6, and 12 months). METHODS: Blood was collected from 32 patients with low and intermediate risk PCa and 12 healthy volunteers. The frequency of immunocompetent cells was identified by flow cytometry. The concentration of immunoglobulins and complements was detected by ELISA. RESULTS: Various immunocompetent cells were dysregulated in PCa patients compared with healthy volunteers. Peripheral serum prostate-specific antigen (PSA) decreased rapidly at the first month after PPB treatment, and the peripheral serum PSA became very low at 6 months after PPB treatment. CD3+ T cells, CD4+ T cells, CD3-CD16+/56+ natural killer (NK) cells were increased significantly at certain time points after PPB. Although the percentage of the CD8+ T cells did not change markedly, the ratio of CD4/CD8 increased significantly at 3 months after PPB (P=0.0196). There was no influence of PPB on B cells number, but the concentration of immunoglobulins IgM, IgG, and IgA, and complements C3 and C4 in patients increased at some time points after PPB. CONCLUSION: The immunocompetent cells are dysregulated in PCa patients. PPB treatment could effectively kill tumor cells and then stimulate cellular immunity and humoral immunity in PCa patients. |
format | Online Article Text |
id | pubmed-5438076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54380762017-05-25 Analysis of immune status after iodine-125 permanent brachytherapy in prostate cancer Du, E Wang, Lin Li, Chang-ying Zhang, Chang-wen Qu, Yan-chun Liu, Ran-lu Xu, Yong Yang, Kuo Zhang, Zhi-hong Onco Targets Ther Original Research BACKGROUND: Permanent prostate brachytherapy (PPB) is an effective treatment choice for low and intermediate risk prostate cancer (PCa). However, the impact of PPB on tumor immune status is still poorly understood. This study aimed to assess the immune status in PCa patients before and at different time points after PPB (1, 3, 6, and 12 months). METHODS: Blood was collected from 32 patients with low and intermediate risk PCa and 12 healthy volunteers. The frequency of immunocompetent cells was identified by flow cytometry. The concentration of immunoglobulins and complements was detected by ELISA. RESULTS: Various immunocompetent cells were dysregulated in PCa patients compared with healthy volunteers. Peripheral serum prostate-specific antigen (PSA) decreased rapidly at the first month after PPB treatment, and the peripheral serum PSA became very low at 6 months after PPB treatment. CD3+ T cells, CD4+ T cells, CD3-CD16+/56+ natural killer (NK) cells were increased significantly at certain time points after PPB. Although the percentage of the CD8+ T cells did not change markedly, the ratio of CD4/CD8 increased significantly at 3 months after PPB (P=0.0196). There was no influence of PPB on B cells number, but the concentration of immunoglobulins IgM, IgG, and IgA, and complements C3 and C4 in patients increased at some time points after PPB. CONCLUSION: The immunocompetent cells are dysregulated in PCa patients. PPB treatment could effectively kill tumor cells and then stimulate cellular immunity and humoral immunity in PCa patients. Dove Medical Press 2017-05-15 /pmc/articles/PMC5438076/ /pubmed/28546760 http://dx.doi.org/10.2147/OTT.S137491 Text en © 2017 Du et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Du, E Wang, Lin Li, Chang-ying Zhang, Chang-wen Qu, Yan-chun Liu, Ran-lu Xu, Yong Yang, Kuo Zhang, Zhi-hong Analysis of immune status after iodine-125 permanent brachytherapy in prostate cancer |
title | Analysis of immune status after iodine-125 permanent brachytherapy in prostate cancer |
title_full | Analysis of immune status after iodine-125 permanent brachytherapy in prostate cancer |
title_fullStr | Analysis of immune status after iodine-125 permanent brachytherapy in prostate cancer |
title_full_unstemmed | Analysis of immune status after iodine-125 permanent brachytherapy in prostate cancer |
title_short | Analysis of immune status after iodine-125 permanent brachytherapy in prostate cancer |
title_sort | analysis of immune status after iodine-125 permanent brachytherapy in prostate cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438076/ https://www.ncbi.nlm.nih.gov/pubmed/28546760 http://dx.doi.org/10.2147/OTT.S137491 |
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