← 返回

骨髓腔内注射工程化乳酸乳球菌治疗转移性肿瘤:初步报告

英文原题:Intra-bone marrow injection with engineered Lactococcus lactis for the treatment of metastatic tumors: Primary report.

查看英文原题

Intra-bone marrow injection with engineered Lactococcus lactis for the treatment of metastatic tumors: Primary report.

PubMed 2024/03/11(内容时间) Biomed Pharmacother

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

骨髓具有产生不同类型免疫细胞的能力,例如NK 细胞、巨噬细胞、树突状细胞(DCs)和T细胞。提高骨髓中免疫细胞的激活可以增强骨转移的治疗效果。此前,我们设计了一种工程化益生菌乳酸乳球菌,能够表达Fms样酪氨酸激酶3配体与共刺激分子OX40配体的融合蛋白(FOLactis),并证明其可诱导多种免疫细胞的激活和分化。在本研究中,我们成功建立了骨转移、肺转移和腹腔播散的小鼠模型,并首次将益生菌直接注射到骨髓中以抑制肿瘤生长。我们观察到,将FOLactis注射到小鼠骨髓中能更好地调节荷瘤小鼠的免疫微环境,从而产生抑瘤效果。与皮下(s.c.)注射相比,骨髓内(IBM)注射在增加成熟DCs和CD8 + T细胞以及延长荷瘤小鼠生存期方面更为有效。我们的结果证实,IBM注射FOLactis重编程了骨髓的免疫微环境,并在多种转移性肿瘤模型中具有显著效果。

展开英文摘要原文

Bone marrow has the capacity to produce different types of immune cells, such as natural killer cells, macrophages, dendritic cells (DCs) and T cells. Improving the activation of immune cells in the bone marrow can enhance the therapy of bone metastases.

Previously, we designed an engineered probiotic Lactococcus lactis, capable of expressing a fusion protein of Fms-like tyrosine kinase 3 ligand and co-stimulator OX40 ligand (FOLactis), and proved that it can induce the activation and differentiation of several immune cells. In this research, we successfully establish mouse models of bone metastasis, lung metastasis and intraperitoneal dissemination, and we are the first to directly inject the probiotics into the bone marrow to inhibit tumor growth.

We observe that injecting FOLactis into the bone marrow of mice can better regulate the immune microenvironment of tumor-bearing mice, resulting in a tumor-suppressive effect. Compared to subcutaneous (s. c.) injection, intra-bone marrow (IBM) injection is more effective in increasing mature DCs and CD8 + T cells and prolonging the survival of tumor-bearing mice.

Our results confirm that IBM injection of FOLactis reprograms the immune microenvironment of bone marrow and has remarkable effectiveness in various metastatic tumor models.

论文信息

作者
Liu R、Zhu J、Chen A、Fan Y、Li L、Mei Y、Wang Y、Wang X
第一作者单位
The Comprehensive Cancer Centre, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, 321 Zhongshan Road, Nanjing 210008, China; The Clinical Cancer Institute of Nanjing University, Nanjing, China; The Comprehensive Cancer Centre, China Pharmaceutical University Nanjing Drum Tower Hospital, 321 Zhongshan Road, Nanjing 210008, China.China
通讯作者单位
The Comprehensive Cancer Centre, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, 321 Zhongshan Road, Nanjing 210008, China; The Clinical Cancer Institute of Nanjing University, Nanjing, China. Electronic address: liuqin@nju.edu.cn.China
期刊
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie2024 Apr
原文标识
PubMed 38471270 · DOI 10.1016/j.biopha.2024.116384