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Nanomaterial-Based Tumor Photothermal Immunotherapy

In recent years, photothermal therapy (PTT) particularly nanomaterial-based PTT is a promising therapeutic modality and technique for cancer tumor ablation. In addition to killing tumor cells directly through heat, PTT also can induce immunogenic cell death (ICD) to activate the whole-body anti-tumo...

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Detalles Bibliográficos
Autores principales: Xu, Peng, Liang, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7684030/
https://www.ncbi.nlm.nih.gov/pubmed/33244232
http://dx.doi.org/10.2147/IJN.S249252
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author Xu, Peng
Liang, Feng
author_facet Xu, Peng
Liang, Feng
author_sort Xu, Peng
collection PubMed
description In recent years, photothermal therapy (PTT) particularly nanomaterial-based PTT is a promising therapeutic modality and technique for cancer tumor ablation. In addition to killing tumor cells directly through heat, PTT also can induce immunogenic cell death (ICD) to activate the whole-body anti-tumor immune response, including the redistribution and activation of immune effector cells, the expression and secretion of cytokines and the transformation of memory T lymphocytes. When used in combination with immunotherapy, the efficacy of nanomaterial-based PTT can be improved. This article summarized the mechanism of nanomaterial-based PTT against cancer and how nanomaterial-based PTT impacts the tumor microenvironment and induces an immune response. Moreover, we reviewed recent advances of nanomaterial-based photothermal immunotherapy and discussed challenges and future outlook.
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spelling pubmed-76840302020-11-25 Nanomaterial-Based Tumor Photothermal Immunotherapy Xu, Peng Liang, Feng Int J Nanomedicine Review In recent years, photothermal therapy (PTT) particularly nanomaterial-based PTT is a promising therapeutic modality and technique for cancer tumor ablation. In addition to killing tumor cells directly through heat, PTT also can induce immunogenic cell death (ICD) to activate the whole-body anti-tumor immune response, including the redistribution and activation of immune effector cells, the expression and secretion of cytokines and the transformation of memory T lymphocytes. When used in combination with immunotherapy, the efficacy of nanomaterial-based PTT can be improved. This article summarized the mechanism of nanomaterial-based PTT against cancer and how nanomaterial-based PTT impacts the tumor microenvironment and induces an immune response. Moreover, we reviewed recent advances of nanomaterial-based photothermal immunotherapy and discussed challenges and future outlook. Dove 2020-11-19 /pmc/articles/PMC7684030/ /pubmed/33244232 http://dx.doi.org/10.2147/IJN.S249252 Text en © 2020 Xu and Liang. http://creativecommons.org/licenses/by-nc/3.0/ 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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Xu, Peng
Liang, Feng
Nanomaterial-Based Tumor Photothermal Immunotherapy
title Nanomaterial-Based Tumor Photothermal Immunotherapy
title_full Nanomaterial-Based Tumor Photothermal Immunotherapy
title_fullStr Nanomaterial-Based Tumor Photothermal Immunotherapy
title_full_unstemmed Nanomaterial-Based Tumor Photothermal Immunotherapy
title_short Nanomaterial-Based Tumor Photothermal Immunotherapy
title_sort nanomaterial-based tumor photothermal immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7684030/
https://www.ncbi.nlm.nih.gov/pubmed/33244232
http://dx.doi.org/10.2147/IJN.S249252
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