Organoid Models for Precision Cancer Immunotherapy

被引:57
作者
Sun, Cai-Ping [1 ]
Lan, Huan-Rong [2 ]
Fang, Xing-Liang [3 ]
Yang, Xiao-Yun [4 ]
Jin, Ke-Tao [5 ]
机构
[1] Zhejiang Univ Sch Med, Shaoxing Peoples Hosp, Shaoxing Hosp, Dept Med Oncol, Shaoxing, Peoples R China
[2] Zhejiang Univ Sch Med, Affiliated Jinhua Hosp, Dept Breast & Thyroid Surg, Jinhua, Peoples R China
[3] Shaoxing Univ, Affiliated Hosp, Shaoxing Municipal Hosp, Coll Med,Dept Hepatobiliary Surg, Shaoxing, Peoples R China
[4] Zhejiang Univ, Affiliated Jinhua Hosp, Sch Med, Dept Gastroenterol, Jinhua, Peoples R China
[5] Zhejiang Univ, Affiliated Jinhua Hosp, Sch Med, Dept Colorectal Surg, Jinhua, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
基金
中国国家自然科学基金;
关键词
cancer; immunotherapy; organoid; precision medicine; tumor microenvironment; IN-VITRO EXPANSION; STEM-CELLS; PERSONALIZED IMMUNOTHERAPY; EPITHELIAL ORGANOIDS; IMMUNE CELLS; SINGLE LGR5; LONG-TERM; T-CELLS; PLATFORM; DIVERSE;
D O I
10.3389/fimmu.2022.770465
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cancer immunotherapy is exploited for the treatment of disease by modulating the immune system. Since the conventional in vivo animal and 2D in vitro models insufficiently recapitulate the complex tumor immune microenvironment (TIME) of the original tumor. In addition, due to the involvement of the immune system in cancer immunotherapy, more physiomimetic cancer models, such as patient-derived organoids (PDOs), are required to evaluate the efficacy of immunotherapy agents. On the other hand, the dynamic interactions between the neoplastic cells and non-neoplastic host components in the TIME can promote carcinogenesis, tumor metastasis, cancer progression, and drug resistance of cancer cells. Indeed, tumor organoid models can properly recapitulate the TIME by preserving endogenous stromal components including various immune cells, or by adding exogenous immune cells, cancer-associated fibroblasts (CAFs), vasculature, and other components. Therefore, organoid culture platforms could model immunotherapy responses and facilitate the immunotherapy preclinical testing. Here, we discuss the various organoid culture approaches for the modeling of TIME and the applications of complex tumor organoids in testing cancer immunotherapeutics and personalized cancer immunotherapy.
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页数:10
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