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高压氧通过调节肿瘤微环境促进免疫治疗的进展。

Advances in hyperbaric oxygen to promote immunotherapy through modulation of the tumor microenvironment.

作者信息

Wang Pei, Wang Xiao-Yan, Man Chang-Feng, Gong Dan-Dan, Fan Yu

机构信息

Cancer Institute, The Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.

Department of Gastroenterology, The Affiliated Suqian First People's Hospital of Xuzhou Medical University, Suqian, Jiangsu, China.

出版信息

Front Oncol. 2023 Sep 15;13:1200619. doi: 10.3389/fonc.2023.1200619. eCollection 2023.

DOI:10.3389/fonc.2023.1200619
PMID:37790761
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10543083/
Abstract

Hyperbaric oxygen therapy is a relatively safe treatment method that has been used for a long time in the clinic. It has been proven that it can enhance the sensitivity of radiotherapy and photodynamic therapy for cancer. However, there are few studies on hyperbaric oxygen and immunotherapy. In this article, we summarize that hyperbaric oxygen therapy regulates the tumor microenvironment through various pathways such as improving tumor hypoxia, targeting hypoxia-inducing factors, and generating reactive oxygen species. The change in the tumor microenvironment ultimately affects the curative effect of immunotherapy. Therefore, hyperbaric oxygen can influence immunotherapy by regulating the tumor microenvironment, providing a direction for the future development of immunotherapy.

摘要

高压氧疗法是一种相对安全的治疗方法,在临床上已应用多年。业已证明,它可增强放疗和光动力疗法对癌症的敏感性。然而,关于高压氧与免疫疗法的研究较少。在本文中,我们总结了高压氧疗法通过改善肿瘤缺氧、靶向缺氧诱导因子和产生活性氧等多种途径调节肿瘤微环境。肿瘤微环境的变化最终影响免疫疗法的疗效。因此,高压氧可通过调节肿瘤微环境影响免疫疗法,为免疫疗法的未来发展提供了方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef76/10543083/80b5f565a4c2/fonc-13-1200619-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef76/10543083/ee40abbef7ae/fonc-13-1200619-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef76/10543083/a3ce2ca7fd35/fonc-13-1200619-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef76/10543083/80b5f565a4c2/fonc-13-1200619-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef76/10543083/ee40abbef7ae/fonc-13-1200619-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef76/10543083/a3ce2ca7fd35/fonc-13-1200619-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef76/10543083/80b5f565a4c2/fonc-13-1200619-g003.jpg

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引用本文的文献

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Cells. 2025 Jul 10;14(14):1057. doi: 10.3390/cells14141057.
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Front Oncol. 2025 Jun 9;15:1580515. doi: 10.3389/fonc.2025.1580515. eCollection 2025.
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本文引用的文献

1
Hyperbaric oxygen protects HT22 cells and PC12 cells from damage caused by oxygen-glucose deprivation/reperfusion via the inhibition of Nrf2/System Xc-/GPX4 axis-mediated ferroptosis.高压氧通过抑制 Nrf2/System Xc-/GPX4 轴介导线粒体铁死亡来保护 HT22 细胞和 PC12 细胞免受氧葡萄糖剥夺/再灌注损伤。
PLoS One. 2022 Nov 10;17(11):e0276083. doi: 10.1371/journal.pone.0276083. eCollection 2022.
2
New scientific definitions: hyperbaric therapy and hyperbaric oxygen therapy.新的科学定义:高压治疗与高压氧治疗。
Med Gas Res. 2023 Apr-Jun;13(2):92-93. doi: 10.4103/2045-9912.356475.
3
Hyperbaric oxygen facilitates teniposide-induced cGAS-STING activation to enhance the antitumor efficacy of PD-1 antibody in HCC.
用于增强光动力诱导免疫治疗的级联充电巨噬细胞仿生钌基纳米电池
J Nanobiotechnology. 2025 Mar 4;23(1):167. doi: 10.1186/s12951-025-03255-8.
4
Hyperbaric Oxygen Therapy as a Novel Approach to Modulating Macrophage Polarization for the Treatment of Glioblastoma.高压氧疗法作为调节巨噬细胞极化治疗胶质母细胞瘤的新方法。
Biomedicines. 2024 Jun 21;12(7):1383. doi: 10.3390/biomedicines12071383.
高压氧促进依托泊苷诱导的 cGAS-STING 激活,增强 PD-1 抗体在 HCC 中的抗肿瘤疗效。
J Immunother Cancer. 2022 Aug;10(8). doi: 10.1136/jitc-2021-004006.
4
Abundance of reactive oxygen species (ROS) is associated with tumor aggressiveness, immune response, and worse survival in breast cancer.活性氧(ROS)的大量存在与乳腺癌的侵袭性、免疫反应和较差的生存有关。
Breast Cancer Res Treat. 2022 Jul;194(2):231-241. doi: 10.1007/s10549-022-06633-0. Epub 2022 May 31.
5
Targeting HIF-1α abrogates PD-L1-mediated immune evasion in tumor microenvironment but promotes tolerance in normal tissues.靶向 HIF-1α 可消除肿瘤微环境中 PD-L1 介导的免疫逃逸,但会促进正常组织中的耐受。
J Clin Invest. 2022 May 2;132(9). doi: 10.1172/JCI150846.
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Aging (Albany NY). 2022 Jan 17;14(2):1048-1064. doi: 10.18632/aging.203833.
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Nat Commun. 2021 Sep 23;12(1):5606. doi: 10.1038/s41467-021-25894-9.