微波消融治疗后工程细菌热反应激活引发抗肿瘤免疫

IF 15.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Yumin Wu, Bo Liu, Yifan Yan, Chuntao Gong, Kaiwei Wang, Nanhui Liu, Yujie Zhu, Maoyi Li, Chunjie Wang, Yizhe Yang, Liangzhu Feng, Zhuang Liu
{"title":"微波消融治疗后工程细菌热反应激活引发抗肿瘤免疫","authors":"Yumin Wu, Bo Liu, Yifan Yan, Chuntao Gong, Kaiwei Wang, Nanhui Liu, Yujie Zhu, Maoyi Li, Chunjie Wang, Yizhe Yang, Liangzhu Feng, Zhuang Liu","doi":"10.1038/s41467-024-54883-x","DOIUrl":null,"url":null,"abstract":"<p>Incomplete tumor removal after microwave ablation (MWA), a widely used hyperthermia-based therapy, can result in tumor recurrence. Herein, attenuated Salmonella typhimurium VNP20009 is engineered to release interleukin-15&amp;interleukin-15-receptor-alpha (IL-15&amp;IL-15Rα) in response to mildly elevated temperature. Such 15&amp;15R@VNP colonizes in tumors upon intravenous injection, and the expression of IL-15&amp;IL-15Rα is triggered by MWA. Anti-tumor immune responses are elicited, efficiently suppressing tumor growth even after incomplete microwave ablation. We further design VNP20009 with thermal-responsive co-expression of both IL-15&amp;IL-15Rα and soluble programmed cell death protein (sPD-1). Such sPD-1-15&amp;15R@VNP can also reverse the functional suppression of immune cells driven by PD-1/PD-L1 axis, reinvigorating progenitor exhausted T cells, a critical subset of cytotoxic T lymphocytes responsive to immune checkpoint blockade. Such thermal-responsive engineered bacteria are thus a promising adjuvant therapy to potentiate tumor ablation therapies via effectively activating antitumor immunity.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"198 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Thermal-responsive activation of engineered bacteria to trigger antitumor immunity post microwave ablation therapy\",\"authors\":\"Yumin Wu, Bo Liu, Yifan Yan, Chuntao Gong, Kaiwei Wang, Nanhui Liu, Yujie Zhu, Maoyi Li, Chunjie Wang, Yizhe Yang, Liangzhu Feng, Zhuang Liu\",\"doi\":\"10.1038/s41467-024-54883-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Incomplete tumor removal after microwave ablation (MWA), a widely used hyperthermia-based therapy, can result in tumor recurrence. Herein, attenuated Salmonella typhimurium VNP20009 is engineered to release interleukin-15&amp;interleukin-15-receptor-alpha (IL-15&amp;IL-15Rα) in response to mildly elevated temperature. Such 15&amp;15R@VNP colonizes in tumors upon intravenous injection, and the expression of IL-15&amp;IL-15Rα is triggered by MWA. Anti-tumor immune responses are elicited, efficiently suppressing tumor growth even after incomplete microwave ablation. We further design VNP20009 with thermal-responsive co-expression of both IL-15&amp;IL-15Rα and soluble programmed cell death protein (sPD-1). Such sPD-1-15&amp;15R@VNP can also reverse the functional suppression of immune cells driven by PD-1/PD-L1 axis, reinvigorating progenitor exhausted T cells, a critical subset of cytotoxic T lymphocytes responsive to immune checkpoint blockade. Such thermal-responsive engineered bacteria are thus a promising adjuvant therapy to potentiate tumor ablation therapies via effectively activating antitumor immunity.</p>\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"198 1\",\"pages\":\"\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2024-12-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Communications\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1038/s41467-024-54883-x\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-024-54883-x","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

微波消融(MWA)是一种广泛应用的基于热疗的不完全切除肿瘤的治疗方法,可导致肿瘤复发。在本研究中,减毒鼠伤寒沙门氏菌VNP20009被设计成在轻度升高的温度下释放白细胞介素-15受体α (IL-15&IL-15Rα)。这种15&;15R@VNP通过静脉注射在肿瘤中定植,并且IL-15&;IL-15Rα的表达是由MWA触发的。诱导抗肿瘤免疫反应,有效抑制肿瘤生长,即使在不完全微波消融后。我们进一步设计了具有热响应性il -15和IL-15Rα和可溶性程序性细胞死亡蛋白(sPD-1)共表达的VNP20009。这样的spd -1-15 15R@VNP也可以逆转PD-1/PD-L1轴驱动的免疫细胞的功能抑制,重新激活祖耗尽T细胞,细胞毒性T淋巴细胞的一个关键亚群,对免疫检查点封锁有反应。因此,这种热反应工程细菌是一种很有希望的辅助治疗,通过有效激活抗肿瘤免疫来增强肿瘤消融治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Thermal-responsive activation of engineered bacteria to trigger antitumor immunity post microwave ablation therapy

Thermal-responsive activation of engineered bacteria to trigger antitumor immunity post microwave ablation therapy

Incomplete tumor removal after microwave ablation (MWA), a widely used hyperthermia-based therapy, can result in tumor recurrence. Herein, attenuated Salmonella typhimurium VNP20009 is engineered to release interleukin-15&interleukin-15-receptor-alpha (IL-15&IL-15Rα) in response to mildly elevated temperature. Such 15&15R@VNP colonizes in tumors upon intravenous injection, and the expression of IL-15&IL-15Rα is triggered by MWA. Anti-tumor immune responses are elicited, efficiently suppressing tumor growth even after incomplete microwave ablation. We further design VNP20009 with thermal-responsive co-expression of both IL-15&IL-15Rα and soluble programmed cell death protein (sPD-1). Such sPD-1-15&15R@VNP can also reverse the functional suppression of immune cells driven by PD-1/PD-L1 axis, reinvigorating progenitor exhausted T cells, a critical subset of cytotoxic T lymphocytes responsive to immune checkpoint blockade. Such thermal-responsive engineered bacteria are thus a promising adjuvant therapy to potentiate tumor ablation therapies via effectively activating antitumor immunity.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信