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Organoid Models for Precision Cancer Immunotherapy

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...

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Autores principales: Sun, Cai-Ping, Lan, Huan-Rong, Fang, Xing-Liang, Yang, Xiao-Yun, Jin, Ke-Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016193/
https://www.ncbi.nlm.nih.gov/pubmed/35450073
http://dx.doi.org/10.3389/fimmu.2022.770465
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author Sun, Cai-Ping
Lan, Huan-Rong
Fang, Xing-Liang
Yang, Xiao-Yun
Jin, Ke-Tao
author_facet Sun, Cai-Ping
Lan, Huan-Rong
Fang, Xing-Liang
Yang, Xiao-Yun
Jin, Ke-Tao
author_sort Sun, Cai-Ping
collection PubMed
description 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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spelling pubmed-90161932022-04-20 Organoid Models for Precision Cancer Immunotherapy Sun, Cai-Ping Lan, Huan-Rong Fang, Xing-Liang Yang, Xiao-Yun Jin, Ke-Tao Front Immunol Immunology 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. Frontiers Media S.A. 2022-04-05 /pmc/articles/PMC9016193/ /pubmed/35450073 http://dx.doi.org/10.3389/fimmu.2022.770465 Text en Copyright © 2022 Sun, Lan, Fang, Yang and Jin https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Sun, Cai-Ping
Lan, Huan-Rong
Fang, Xing-Liang
Yang, Xiao-Yun
Jin, Ke-Tao
Organoid Models for Precision Cancer Immunotherapy
title Organoid Models for Precision Cancer Immunotherapy
title_full Organoid Models for Precision Cancer Immunotherapy
title_fullStr Organoid Models for Precision Cancer Immunotherapy
title_full_unstemmed Organoid Models for Precision Cancer Immunotherapy
title_short Organoid Models for Precision Cancer Immunotherapy
title_sort organoid models for precision cancer immunotherapy
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016193/
https://www.ncbi.nlm.nih.gov/pubmed/35450073
http://dx.doi.org/10.3389/fimmu.2022.770465
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