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Microbial hydrogen “manufactory” for enhanced gas therapy and self-activated immunotherapy via reduced immune escape
BACKGROUND: As an antioxidant, hydrogen (H(2)) can selectively react with the highly toxic hydroxyl radical (·OH) in tumor cells to break the balance of reactive oxygen species (ROS) and cause oxidative stress. However, due to the high diffusibility and storage difficulty of hydrogen, it is impossib...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9199139/ https://www.ncbi.nlm.nih.gov/pubmed/35705974 http://dx.doi.org/10.1186/s12951-022-01440-7 |
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author | Yan, Hongyu Fan, Miao Liu, Huifang Xiao, Tingshan Han, Dandan Che, Ruijun Zhang, Wei Zhou, Xiaohan Wang, June Zhang, Chi Yang, Xinjian Zhang, Jinchao Li, Zhenhua |
author_facet | Yan, Hongyu Fan, Miao Liu, Huifang Xiao, Tingshan Han, Dandan Che, Ruijun Zhang, Wei Zhou, Xiaohan Wang, June Zhang, Chi Yang, Xinjian Zhang, Jinchao Li, Zhenhua |
author_sort | Yan, Hongyu |
collection | PubMed |
description | BACKGROUND: As an antioxidant, hydrogen (H(2)) can selectively react with the highly toxic hydroxyl radical (·OH) in tumor cells to break the balance of reactive oxygen species (ROS) and cause oxidative stress. However, due to the high diffusibility and storage difficulty of hydrogen, it is impossible to achieve long-term release at the tumor site, which highly limited their therapeutic effect. RESULTS: Photosynthetic bacteria (PSB) release a large amount of hydrogen to break the balance of oxidative stress. In addition, as a nontoxic bacterium, PSB could stimulate the immune response and increase the infiltration of CD4+ and CD8+ T cells. More interestingly, we found that hydrogen therapy induced by our live PSB did not lead to the up-regulation of PD-L1 after stimulating the immune response, which could avoid the tumor immune escape. CONCLUSION: Hydrogen-immunotherapy significantly kills tumor cells. We believe that our live microbial hydrogen production system provides a new strategy for cancer hydrogen treatment combining with enhanced immunotherapy without up-regulating PD-L1. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01440-7. |
format | Online Article Text |
id | pubmed-9199139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91991392022-06-16 Microbial hydrogen “manufactory” for enhanced gas therapy and self-activated immunotherapy via reduced immune escape Yan, Hongyu Fan, Miao Liu, Huifang Xiao, Tingshan Han, Dandan Che, Ruijun Zhang, Wei Zhou, Xiaohan Wang, June Zhang, Chi Yang, Xinjian Zhang, Jinchao Li, Zhenhua J Nanobiotechnology Research BACKGROUND: As an antioxidant, hydrogen (H(2)) can selectively react with the highly toxic hydroxyl radical (·OH) in tumor cells to break the balance of reactive oxygen species (ROS) and cause oxidative stress. However, due to the high diffusibility and storage difficulty of hydrogen, it is impossible to achieve long-term release at the tumor site, which highly limited their therapeutic effect. RESULTS: Photosynthetic bacteria (PSB) release a large amount of hydrogen to break the balance of oxidative stress. In addition, as a nontoxic bacterium, PSB could stimulate the immune response and increase the infiltration of CD4+ and CD8+ T cells. More interestingly, we found that hydrogen therapy induced by our live PSB did not lead to the up-regulation of PD-L1 after stimulating the immune response, which could avoid the tumor immune escape. CONCLUSION: Hydrogen-immunotherapy significantly kills tumor cells. We believe that our live microbial hydrogen production system provides a new strategy for cancer hydrogen treatment combining with enhanced immunotherapy without up-regulating PD-L1. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01440-7. BioMed Central 2022-06-15 /pmc/articles/PMC9199139/ /pubmed/35705974 http://dx.doi.org/10.1186/s12951-022-01440-7 Text en © The Author(s) 2022 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 | Research Yan, Hongyu Fan, Miao Liu, Huifang Xiao, Tingshan Han, Dandan Che, Ruijun Zhang, Wei Zhou, Xiaohan Wang, June Zhang, Chi Yang, Xinjian Zhang, Jinchao Li, Zhenhua Microbial hydrogen “manufactory” for enhanced gas therapy and self-activated immunotherapy via reduced immune escape |
title | Microbial hydrogen “manufactory” for enhanced gas therapy and self-activated immunotherapy via reduced immune escape |
title_full | Microbial hydrogen “manufactory” for enhanced gas therapy and self-activated immunotherapy via reduced immune escape |
title_fullStr | Microbial hydrogen “manufactory” for enhanced gas therapy and self-activated immunotherapy via reduced immune escape |
title_full_unstemmed | Microbial hydrogen “manufactory” for enhanced gas therapy and self-activated immunotherapy via reduced immune escape |
title_short | Microbial hydrogen “manufactory” for enhanced gas therapy and self-activated immunotherapy via reduced immune escape |
title_sort | microbial hydrogen “manufactory” for enhanced gas therapy and self-activated immunotherapy via reduced immune escape |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9199139/ https://www.ncbi.nlm.nih.gov/pubmed/35705974 http://dx.doi.org/10.1186/s12951-022-01440-7 |
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