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Advances in technology and applications of nanoimmunotherapy for cancer

Host-tumor immune interactions play critical roles in the natural history of tumors, including oncogenesis, progress and metastasis. On the one hand, neoantigens have the potential to drive a tumor-specific immune response. In tumors, immunogenic cell death (ICD) triggered by various inducers can in...

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Autores principales: Dou, Lei, Meng, Xiangdan, Yang, Huiyuan, Dong, Haifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379775/
https://www.ncbi.nlm.nih.gov/pubmed/34419164
http://dx.doi.org/10.1186/s40364-021-00321-9
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author Dou, Lei
Meng, Xiangdan
Yang, Huiyuan
Dong, Haifeng
author_facet Dou, Lei
Meng, Xiangdan
Yang, Huiyuan
Dong, Haifeng
author_sort Dou, Lei
collection PubMed
description Host-tumor immune interactions play critical roles in the natural history of tumors, including oncogenesis, progress and metastasis. On the one hand, neoantigens have the potential to drive a tumor-specific immune response. In tumors, immunogenic cell death (ICD) triggered by various inducers can initiate a strong host anti-immune response. On the other hand, the tolerogenic tumor immune microenvironment suppresses host immune responses that eradicate tumor cells and impair the effect of tumor therapy. Therefore, a deeper understanding and more effective manipulation of the intricate host-tumor immune interaction involving the host, tumor cells and the corresponding tumor immune microenvironment are required. Despite the encouraging breakthroughs resulting from tumor immunotherapy, no single strategy has elicited sufficient or sustained antitumor immune responses in most patients with specific malignancies due to limited activation of specific antitumor immune responses and inadequate remodeling of the tolerogenic tumor immune microenvironment. However, nanotechnology provides a unique paradigm to simultaneously tackle all these challenges, including effective “targeted” delivery of tumor antigens, sustained ICD mediation, and “cold” tumor microenvironment remodeling. In this review, we focus on several key concepts in host-tumor immune interactions and discuss the corresponding therapeutic strategy based on the application of nanoparticles.
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spelling pubmed-83797752021-08-23 Advances in technology and applications of nanoimmunotherapy for cancer Dou, Lei Meng, Xiangdan Yang, Huiyuan Dong, Haifeng Biomark Res Review Host-tumor immune interactions play critical roles in the natural history of tumors, including oncogenesis, progress and metastasis. On the one hand, neoantigens have the potential to drive a tumor-specific immune response. In tumors, immunogenic cell death (ICD) triggered by various inducers can initiate a strong host anti-immune response. On the other hand, the tolerogenic tumor immune microenvironment suppresses host immune responses that eradicate tumor cells and impair the effect of tumor therapy. Therefore, a deeper understanding and more effective manipulation of the intricate host-tumor immune interaction involving the host, tumor cells and the corresponding tumor immune microenvironment are required. Despite the encouraging breakthroughs resulting from tumor immunotherapy, no single strategy has elicited sufficient or sustained antitumor immune responses in most patients with specific malignancies due to limited activation of specific antitumor immune responses and inadequate remodeling of the tolerogenic tumor immune microenvironment. However, nanotechnology provides a unique paradigm to simultaneously tackle all these challenges, including effective “targeted” delivery of tumor antigens, sustained ICD mediation, and “cold” tumor microenvironment remodeling. In this review, we focus on several key concepts in host-tumor immune interactions and discuss the corresponding therapeutic strategy based on the application of nanoparticles. BioMed Central 2021-08-21 /pmc/articles/PMC8379775/ /pubmed/34419164 http://dx.doi.org/10.1186/s40364-021-00321-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Dou, Lei
Meng, Xiangdan
Yang, Huiyuan
Dong, Haifeng
Advances in technology and applications of nanoimmunotherapy for cancer
title Advances in technology and applications of nanoimmunotherapy for cancer
title_full Advances in technology and applications of nanoimmunotherapy for cancer
title_fullStr Advances in technology and applications of nanoimmunotherapy for cancer
title_full_unstemmed Advances in technology and applications of nanoimmunotherapy for cancer
title_short Advances in technology and applications of nanoimmunotherapy for cancer
title_sort advances in technology and applications of nanoimmunotherapy for cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379775/
https://www.ncbi.nlm.nih.gov/pubmed/34419164
http://dx.doi.org/10.1186/s40364-021-00321-9
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