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干扰素-γ通过增加M1巨噬细胞、CD4和CD8 T细胞数量并减少中性粒细胞数量,增强减毒介导的癌症免疫疗法的抗肿瘤活性。

IFN-γ enhances the antitumor activity of attenuated -mediated cancer immunotherapy by increasing M1 macrophage and CD4 and CD8 T cell counts and decreasing neutrophil counts.

作者信息

Xu Huimin, Piao Linghua, Wu Yundi, Liu Xiande

机构信息

School of Life Sciences, Hainan University, Haikou, China.

Department of Physiology, Hainan Medical University, Haikou, China.

出版信息

Front Bioeng Biotechnol. 2022 Sep 29;10:996055. doi: 10.3389/fbioe.2022.996055. eCollection 2022.

DOI:10.3389/fbioe.2022.996055
PMID:36246355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9556780/
Abstract

Bacteria-mediated cancer immunotherapy (BCI) inhibits tumor progression and has a synergistic antitumor effect when combined with chemotherapy. The anti- or pro-tumorigenic effects of interferon-γ (IFN-γ) are controversial; hence, we were interested in the antitumor effects of IFN-γ/BCI combination therapy. Here, we demonstrated that IFN-γ increased the tumor cell killing efficacy of attenuated by prolonging the survival of tumor-colonizing bacteria blockade of tumor-infiltrating neutrophil recruitment. In addition, IFN-γ attenuated -stimulated immune responses by stimulating tumor infiltration by M1-like macrophages and CD4 and CD8 T cells, thereby facilitating tumor eradication. Taken together, these findings suggest that combination treatment with IFN-γ boosts the therapeutic response of BCI with S. tΔppGpp, suggesting that IFN-γ/BCI is a promising approach to immunotherapy.

摘要

细菌介导的癌症免疫疗法(BCI)可抑制肿瘤进展,与化疗联合使用时具有协同抗肿瘤作用。干扰素-γ(IFN-γ)的抗肿瘤或促肿瘤作用存在争议;因此,我们对IFN-γ/BCI联合疗法的抗肿瘤作用感兴趣。在此,我们证明,IFN-γ通过延长肿瘤定植细菌的存活时间、阻断肿瘤浸润性中性粒细胞募集,提高了减毒细菌的肿瘤细胞杀伤效力。此外,IFN-γ通过刺激M1样巨噬细胞、CD4和CD8 T细胞浸润肿瘤,减弱了细菌刺激的免疫反应,从而促进肿瘤根除。综上所述,这些发现表明,IFN-γ联合治疗可增强BCI与鼠伤寒沙门氏菌ΔppGpp的治疗反应,提示IFN-γ/BCI是一种有前景的免疫治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/958f0f9718f9/fbioe-10-996055-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/d5f970d62b5f/fbioe-10-996055-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/298743749821/fbioe-10-996055-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/5aba37db3663/fbioe-10-996055-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/5b596d575602/fbioe-10-996055-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/b866512e467c/fbioe-10-996055-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/983a36c2aade/fbioe-10-996055-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/2778a1dc6d8e/fbioe-10-996055-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/958f0f9718f9/fbioe-10-996055-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/d5f970d62b5f/fbioe-10-996055-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/298743749821/fbioe-10-996055-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/5aba37db3663/fbioe-10-996055-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/5b596d575602/fbioe-10-996055-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/b866512e467c/fbioe-10-996055-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/983a36c2aade/fbioe-10-996055-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/2778a1dc6d8e/fbioe-10-996055-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9556780/958f0f9718f9/fbioe-10-996055-g008.jpg

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Nat Commun. 2021 Jun 10;12(1):3530. doi: 10.1038/s41467-021-23164-2.
2
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Front Immunol. 2020 Dec 3;11:583084. doi: 10.3389/fimmu.2020.583084. eCollection 2020.
3
M1 tumor-associated macrophages boost tissue-resident memory T cells infiltration and survival in human lung cancer.M1 肿瘤相关巨噬细胞促进人类肺癌中组织驻留记忆 T 细胞的浸润和存活。
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iScience. 2024 Dec 16;28(1):111614. doi: 10.1016/j.isci.2024.111614. eCollection 2025 Jan 17.
4
The ovarian cancer-associated microbiome contributes to the tumor's inflammatory microenvironment.卵巢癌相关的微生物组有助于肿瘤的炎症微环境。
Front Cell Infect Microbiol. 2024 Oct 21;14:1440742. doi: 10.3389/fcimb.2024.1440742. eCollection 2024.
5
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Sci Immunol. 2024 Oct 18;9(100):eadn9879. doi: 10.1126/sciimmunol.adn9879.
6
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