High-dose VitC plus oncolytic adenoviruses enhance immunogenic tumor cell death and reprogram tumor immune microenvironment
2022-02-02
发表期刊MOLECULAR THERAPY (IF:12.1[JCR-2023],11.8[5-Year])
ISSN1525-0016
EISSN1525-0024
卷号30期号:2
发表状态已发表
DOI10.1016/j.ymthe.2021.09.015
摘要Preclinical and clinical studies have validated the antitumor effects of several oncolytic viruses (OVs). However, the efficacy of OVs is limited when they are administered as monotherapies. Combination therapy is a promising direction for oncolytic virotherapy in the future. A high dose of vitamin C (VitC) exerts anticancer effects by triggering the accretion of substantial amounts of reactive oxygen species (ROS). OVs can induce immunogenic tumor cell death and elicit an antitumor immune response. ROS play an important role in immunogenic cell death (ICD). This study aimed to explore whether highdose VitC in combination with oncolytic adenoviruses (oAds) exhibited a synergistic antitumor effect. High-dose VitC synergized with oAds against tumor by enhancing immunogenic tumor cell death. Combination therapy with high-dose VitC and oAds significantly increased the number of T cells in the tumor microenvironment (TME) and promoted the activation of T cells. Furthermore, the antitumor effect of the combination therapy was CD8+ T cell dependent. In addition, combination therapy with high-dose VitC and oAds reprogramed the immunosuppressive TME. Our study provides a new strategy for combination therapy of OVs.
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收录类别SCI ; SCIE
语种英语
资助项目National Science and Technology Major Projects of New Drugs[2018ZX09201018-013] ; National Science and Technology Major Projects for Infectious Diseases Control[2017ZX10203206-004] ; National Natural Science Foundation of China[81101728,82070660] ; Sichuan Regional Innovation Cooperation Project[20QYCX0100] ; Innovation Spark Project of Sichuan University[2018SCUH0084]
WOS研究方向Biotechnology & Applied Microbiology ; Genetics & Heredity ; Research & Experimental Medicine
WOS类目Biotechnology & Applied Microbiology ; Genetics & Heredity ; Medicine, Research & Experimental
WOS记录号WOS:000752514200001
出版者CELL PRESS
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文献类型期刊论文
条目标识符https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/155855
专题生命科学与技术学院_PI研究组_许文青组
通讯作者Cheng, Ping
作者单位
1.Sichuan Univ, West China Hosp, State Key Lab Biotherapy & Canc Ctr, Collaborat Innovat Ctr Biotherapy, 17 Peoples South Rd, Chengdu 610041, Peoples R China
2.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
3.Chengdu Fifth Peoples Hosp, Dept Pathol, Chengdu, Peoples R China
4.Sichuan Univ, West China Hosp, Dept Thorac Oncol, Ctr Canc, Chengdu 610041, Peoples R China
5.Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu 610041, Peoples R China
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Ma, Jinhu,Zhang, Chunxue,Shi, Gang,et al. High-dose VitC plus oncolytic adenoviruses enhance immunogenic tumor cell death and reprogram tumor immune microenvironment[J]. MOLECULAR THERAPY,2022,30(2).
APA Ma, Jinhu.,Zhang, Chunxue.,Shi, Gang.,Yue, Dan.,Shu, Yongheng.,...&Cheng, Ping.(2022).High-dose VitC plus oncolytic adenoviruses enhance immunogenic tumor cell death and reprogram tumor immune microenvironment.MOLECULAR THERAPY,30(2).
MLA Ma, Jinhu,et al."High-dose VitC plus oncolytic adenoviruses enhance immunogenic tumor cell death and reprogram tumor immune microenvironment".MOLECULAR THERAPY 30.2(2022).
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