Combination Therapy of TGF-β Blockade and Commensal-derived Probiotics Provides Enhanced Antitumor Immune Response and Tumor Suppression

被引:84
作者
Shi, Linlin [1 ]
Sheng, Jianyong [1 ]
Wang, Mengli [2 ]
Luo, Han [1 ]
Zhu, Jun [3 ,4 ]
Zhang, Bixiang [5 ]
Liu, Zhi [3 ]
Yang, Xiangliang [1 ]
机构
[1] Huazhong Univ Sci & Technol, Coll Life Sci & Technol, Natl Engn Res Ctr Nanomed, Wuhan 430074, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Coll Life Sci & Technol, Ctr Human Genome Res, Key Lab Mol Biophys,Minist Educ, Wuhan 430074, Hubei, Peoples R China
[3] Huazhong Univ Sci & Technol, Dept Biotechnol, Coll Life Sci & Technol, Wuhan 430074, Hubei, Peoples R China
[4] Univ Penn, Perelman Sch Med, Dept Microbiol, Philadelphia, PA 19104 USA
[5] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Hepat Surg Ctr, Wuhan 430030, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
TGF-beta blockade; immunotherapy; gut microbiota; cancer treatment; tumor immune microenvironment; GALUNISERTIB LY2157299 MONOHYDRATE; CANCER PROGRESSION; NISSLE; 1917; MICROBIOTA; INHIBITOR; SYSTEM; MICROENVIRONMENT; IMMUNOTHERAPY; CHECKPOINTS; MECHANISMS;
D O I
10.7150/thno.35131
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Galunisertib (Gal) is a transforming growth factor (TGF-beta) blockade which is being investigated as a potential tumor immunotherapy candidate drug in clinical trials. However, primary or acquired resistance is often found in the recruited cancer patients, which limits its clinical application. Tumor immune microenvironment can be regulated by intestinal microbiota, leading to different therapeutic outcomes. It is hypothesized that manipulation of cancer patients' intestinal microbiome in the early stage of therapy may be a promising strategy to improve the therapeutic efficacy of Gal. Methods: 4T1 and H22 subcutaneous tumor bearing mice were used to evaluate the therapeutic effect. Escherichia coli strain Nissle 1917 (EcN), a widely used probiotic bacteria, was orally delivered to the tumor bearing mice daily along with Gal treatment. Antitumor effect of the combination therapy was evaluated by tumor volume, histological staining of tumor tissues. Furthermore, flow cytometry was performed to analyze the alteration of immune microenvironment in tumor bed after treatment. The suppressing effect of the combination therapy on tumor invasiveness and metastasis was evaluated in both mice and zebrafish xenografts models. Fecal sample 16S rRNA gene sequencing was conducted to analyze changes of intestinal microbial diversity. The effect of intestinal microbiota on tumor suppression after receiving EcN was further tested by fecal transplant. Results: The therapeutic outcomes in tumor growth inhibition and metastasis suppression of Gal were significantly potentiated by EcN, resulting from the strengthened antitumor immunity. EcN was able to relieve the immunosuppressive tumor microenvironment, which was evidenced by enhanced tumor-specific effector T cells infiltration and dendritic cells activation. Intestinal microbiota was modulated by EcN, illustrated by a shift of gut microbiome toward certain beneficial bacteria. Conclusion: These results suggested that Gal combined with EcN might be a novel therapeutic approach with great potential of clinical implications for cancer prevention or treatment.
引用
收藏
页码:4115 / 4129
页数:15
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