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Improving the therapeutic efficacy of oncolytic viruses for cancer: targeting macrophages
Oncolytic viruses (OVs) for cancer treatment are in a rapid stage of development, and the direct tumor lysis and activation of a comprehensive host immune response are irreplaceable advantages of cancer immunotherapy. However, excessive antiviral immune responses also restrict the spread of OVs in v...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666393/ https://www.ncbi.nlm.nih.gov/pubmed/37993941 http://dx.doi.org/10.1186/s12967-023-04709-z |
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author | Shen, Zhen Liu, Xiyu Fan, Guixiang Na, Jintong Liu, Qiaoqiao Lin, Faquan Zhang, Zhikun Zhong, Liping |
author_facet | Shen, Zhen Liu, Xiyu Fan, Guixiang Na, Jintong Liu, Qiaoqiao Lin, Faquan Zhang, Zhikun Zhong, Liping |
author_sort | Shen, Zhen |
collection | PubMed |
description | Oncolytic viruses (OVs) for cancer treatment are in a rapid stage of development, and the direct tumor lysis and activation of a comprehensive host immune response are irreplaceable advantages of cancer immunotherapy. However, excessive antiviral immune responses also restrict the spread of OVs in vivo and the infection of tumor cells. Macrophages are functionally diverse innate immune cells that phagocytose tumor cells and present antigens to activate the immune response, while also limiting the delivery of OVs to tumors. Studies have shown that the functional propensity of macrophages between OVs and tumor cells affects the overall therapeutic effect of oncolytic virotherapy. How to effectively avoid the restrictive effect of macrophages on OVs and reshape the function of tumor-associated macrophages in oncolytic virotherapy is an important challenge we are now facing. Here, we review and summarize the complex dual role of macrophages in oncolytic virotherapy, highlighting how the functional characteristics of macrophage plasticity can be utilized to cooperate with OVs to enhance anti-tumor effects, as well as highlighting the importance of designing and optimizing delivery modalities for OVs in the future. |
format | Online Article Text |
id | pubmed-10666393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106663932023-11-22 Improving the therapeutic efficacy of oncolytic viruses for cancer: targeting macrophages Shen, Zhen Liu, Xiyu Fan, Guixiang Na, Jintong Liu, Qiaoqiao Lin, Faquan Zhang, Zhikun Zhong, Liping J Transl Med Review Oncolytic viruses (OVs) for cancer treatment are in a rapid stage of development, and the direct tumor lysis and activation of a comprehensive host immune response are irreplaceable advantages of cancer immunotherapy. However, excessive antiviral immune responses also restrict the spread of OVs in vivo and the infection of tumor cells. Macrophages are functionally diverse innate immune cells that phagocytose tumor cells and present antigens to activate the immune response, while also limiting the delivery of OVs to tumors. Studies have shown that the functional propensity of macrophages between OVs and tumor cells affects the overall therapeutic effect of oncolytic virotherapy. How to effectively avoid the restrictive effect of macrophages on OVs and reshape the function of tumor-associated macrophages in oncolytic virotherapy is an important challenge we are now facing. Here, we review and summarize the complex dual role of macrophages in oncolytic virotherapy, highlighting how the functional characteristics of macrophage plasticity can be utilized to cooperate with OVs to enhance anti-tumor effects, as well as highlighting the importance of designing and optimizing delivery modalities for OVs in the future. BioMed Central 2023-11-22 /pmc/articles/PMC10666393/ /pubmed/37993941 http://dx.doi.org/10.1186/s12967-023-04709-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Shen, Zhen Liu, Xiyu Fan, Guixiang Na, Jintong Liu, Qiaoqiao Lin, Faquan Zhang, Zhikun Zhong, Liping Improving the therapeutic efficacy of oncolytic viruses for cancer: targeting macrophages |
title | Improving the therapeutic efficacy of oncolytic viruses for cancer: targeting macrophages |
title_full | Improving the therapeutic efficacy of oncolytic viruses for cancer: targeting macrophages |
title_fullStr | Improving the therapeutic efficacy of oncolytic viruses for cancer: targeting macrophages |
title_full_unstemmed | Improving the therapeutic efficacy of oncolytic viruses for cancer: targeting macrophages |
title_short | Improving the therapeutic efficacy of oncolytic viruses for cancer: targeting macrophages |
title_sort | improving the therapeutic efficacy of oncolytic viruses for cancer: targeting macrophages |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666393/ https://www.ncbi.nlm.nih.gov/pubmed/37993941 http://dx.doi.org/10.1186/s12967-023-04709-z |
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