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负载表达外源性白细胞介素-15的重组耻垢分枝杆菌的热敏水凝胶在腹部转移中的治疗效果

The therapeutic effect of thermo-sensitive hydrogel loaded with recombinant mycobacterium smegmatis expressing exogenous IL-15 in abdominal metastasis.

作者信息

Wang Qi, Mei Yi, Rao Wenmei, Hong Sen, Chen Aoxing, Yang Yang, Liu Qin

机构信息

Department of Oncology, Nanjing Drum Tower Hospital, Clinical College of Nanjing Drum Tower Hospital, Nanjing University of Chinese Medicine, 321 Zhongshan Road, Nanjing, 210008, China.

Department of Oncology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, School of Life Sciences, Nanjing University, Nanjing, China.

出版信息

J Transl Med. 2025 May 6;23(1):509. doi: 10.1186/s12967-025-06454-x.

DOI:10.1186/s12967-025-06454-x
PMID:40329350
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12057015/
Abstract

BACKGROUND

Tumor immunotherapy is one of the most promising strategies in cancer treatment. Specifically, intraperitoneal immunotherapy has emerged as a novel approach for dealing with abdominal metastases. Previously, we developed a genetically engineered strain of Mycobacterium smegmatis (Ms-IL15) that expresses the cytokine interleukin-15 (IL15), demonstrating significant anti-tumor effects after intratumoral injection. However, intratumoral infusion might not be feasible in the case of diffuse abdominal metastases, making intraperitoneal injection a preferred option.

METHODS

In this study, we developed a bacterial delivery system by incorporating Ms-IL15 into Poloxamer 407, an injectable thermosensitive hydrogel, for intraperitoneal administration. A murine model of peritoneal metastasis was established, and tumor-bearing mice were administered P407/Ms-IL15 once weekly for two consecutive weeks. The anti-tumor efficacy and alterations in the tumor immune microenvironment were systematically evaluated.

RESULTS

Intraperitoneal injection of this system exhibited a remarkable tumor-suppressive effect, significantly prolonging the survival of treated mice. Flow cytometric analysis of the tumor immune microenvironment revealed enhanced maturation and activation of dendritic cells (DC), an increased proportion of effector memory T cells and Granzyme B, and suppressed macrophage polarization towards the M2 phenotype.

CONCLUSIONS

Our findings indicate that a hydrogel-based bacterial delivery system is a safe and effective approach for the treatment of abdominal metastases.

摘要

背景

肿瘤免疫疗法是癌症治疗中最具前景的策略之一。具体而言,腹腔内免疫疗法已成为一种处理腹部转移瘤的新方法。此前,我们构建了一种表达细胞因子白细胞介素-15(IL15)的基因工程耻垢分枝杆菌菌株(Ms-IL15),瘤内注射后显示出显著的抗肿瘤作用。然而,对于弥漫性腹部转移瘤,瘤内注射可能不可行,使得腹腔注射成为首选方案。

方法

在本研究中,我们通过将Ms-IL15掺入泊洛沙姆407(一种可注射的热敏水凝胶)中开发了一种细菌递送系统,用于腹腔给药。建立了腹膜转移的小鼠模型,给荷瘤小鼠每周腹腔注射一次P407/Ms-IL15,连续注射两周。系统评估了抗肿瘤疗效和肿瘤免疫微环境的变化。

结果

腹腔注射该系统显示出显著的肿瘤抑制作用,显著延长了治疗小鼠的生存期。对肿瘤免疫微环境的流式细胞术分析显示,树突状细胞(DC)的成熟和活化增强,效应记忆T细胞和颗粒酶B的比例增加,巨噬细胞向M2表型的极化受到抑制。

结论

我们的研究结果表明,基于水凝胶的细菌递送系统是治疗腹部转移瘤的一种安全有效的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/36b387b51bca/12967_2025_6454_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/fe2f87ef3912/12967_2025_6454_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/1dcd03257428/12967_2025_6454_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/131f08ccb775/12967_2025_6454_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/53351b9bbe52/12967_2025_6454_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/8853a7932cce/12967_2025_6454_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/8ccb071676b8/12967_2025_6454_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/dd8de3a3a871/12967_2025_6454_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/36b387b51bca/12967_2025_6454_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/fe2f87ef3912/12967_2025_6454_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/1dcd03257428/12967_2025_6454_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/131f08ccb775/12967_2025_6454_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/53351b9bbe52/12967_2025_6454_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/8853a7932cce/12967_2025_6454_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/8ccb071676b8/12967_2025_6454_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/dd8de3a3a871/12967_2025_6454_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9340/12057015/36b387b51bca/12967_2025_6454_Fig7_HTML.jpg

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