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Dual-responsive nanosystem based on TGF-β blockade and immunogenic chemotherapy for effective chemoimmunotherapy

The antitumor immune response induced by chemotherapy has attracted considerable attention. However, the immunosuppressive tumor microenvironment hinders the immune activation effect of cancer chemotherapy. TGF-β plays a key role in driving tumor immunosuppression and can prevent effective antitumor...

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Autores principales: Huang, Xiaoxian, Han, Lingfei, Wang, Ruyi, Zhu, Wanfang, Zhang, Ning, Qu, Wei, Liu, Wenyuan, Liu, Fulei, Feng, Feng, Xue, Jingwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090387/
https://www.ncbi.nlm.nih.gov/pubmed/35506467
http://dx.doi.org/10.1080/10717544.2022.2069877
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author Huang, Xiaoxian
Han, Lingfei
Wang, Ruyi
Zhu, Wanfang
Zhang, Ning
Qu, Wei
Liu, Wenyuan
Liu, Fulei
Feng, Feng
Xue, Jingwei
author_facet Huang, Xiaoxian
Han, Lingfei
Wang, Ruyi
Zhu, Wanfang
Zhang, Ning
Qu, Wei
Liu, Wenyuan
Liu, Fulei
Feng, Feng
Xue, Jingwei
author_sort Huang, Xiaoxian
collection PubMed
description The antitumor immune response induced by chemotherapy has attracted considerable attention. However, the immunosuppressive tumor microenvironment hinders the immune activation effect of cancer chemotherapy. TGF-β plays a key role in driving tumor immunosuppression and can prevent effective antitumor immune response through multiple roles. In this study, a dual-responsive prodrug micelle (PAOL) is designed to co-deliver LY2109761 (a TGF-β receptor I/II inhibitor) and oxaliplatin (OXA, a conventional chemotherapy) to remodel tumor microenvironment and trigger immunogenic cell death (ICD) to induce antitumor immunity response. Under hypoxia tumor environment, the polyethylene glycol shell of the micelle cleavages, along with the release of LY2109761 and OXA prodrug. Cytotoxic effect of OXA is then activated by glutathione-mediated reduction in tumor cells and the activated OXA significantly enhances tumor immunogenicity and promotes intratumoral accumulation of cytotoxic T lymphocytes. Meanwhile, TGF-β blockade through LY2109761 reprograms tumor microenvironment by correcting the immunosuppressive state and regulating tumor extracellular matrix, which further maintaining OXA induced immune response. Therefore, due to the capability of boosting tumor-specific antitumor immunity, the bifunctional micelle presents markedly synergistic antitumor efficacies and provides a potent therapeutic strategy for chemoimmunotherapy of solid tumors.
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spelling pubmed-90903872022-05-11 Dual-responsive nanosystem based on TGF-β blockade and immunogenic chemotherapy for effective chemoimmunotherapy Huang, Xiaoxian Han, Lingfei Wang, Ruyi Zhu, Wanfang Zhang, Ning Qu, Wei Liu, Wenyuan Liu, Fulei Feng, Feng Xue, Jingwei Drug Deliv Research Articles The antitumor immune response induced by chemotherapy has attracted considerable attention. However, the immunosuppressive tumor microenvironment hinders the immune activation effect of cancer chemotherapy. TGF-β plays a key role in driving tumor immunosuppression and can prevent effective antitumor immune response through multiple roles. In this study, a dual-responsive prodrug micelle (PAOL) is designed to co-deliver LY2109761 (a TGF-β receptor I/II inhibitor) and oxaliplatin (OXA, a conventional chemotherapy) to remodel tumor microenvironment and trigger immunogenic cell death (ICD) to induce antitumor immunity response. Under hypoxia tumor environment, the polyethylene glycol shell of the micelle cleavages, along with the release of LY2109761 and OXA prodrug. Cytotoxic effect of OXA is then activated by glutathione-mediated reduction in tumor cells and the activated OXA significantly enhances tumor immunogenicity and promotes intratumoral accumulation of cytotoxic T lymphocytes. Meanwhile, TGF-β blockade through LY2109761 reprograms tumor microenvironment by correcting the immunosuppressive state and regulating tumor extracellular matrix, which further maintaining OXA induced immune response. Therefore, due to the capability of boosting tumor-specific antitumor immunity, the bifunctional micelle presents markedly synergistic antitumor efficacies and provides a potent therapeutic strategy for chemoimmunotherapy of solid tumors. Taylor & Francis 2022-05-04 /pmc/articles/PMC9090387/ /pubmed/35506467 http://dx.doi.org/10.1080/10717544.2022.2069877 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Huang, Xiaoxian
Han, Lingfei
Wang, Ruyi
Zhu, Wanfang
Zhang, Ning
Qu, Wei
Liu, Wenyuan
Liu, Fulei
Feng, Feng
Xue, Jingwei
Dual-responsive nanosystem based on TGF-β blockade and immunogenic chemotherapy for effective chemoimmunotherapy
title Dual-responsive nanosystem based on TGF-β blockade and immunogenic chemotherapy for effective chemoimmunotherapy
title_full Dual-responsive nanosystem based on TGF-β blockade and immunogenic chemotherapy for effective chemoimmunotherapy
title_fullStr Dual-responsive nanosystem based on TGF-β blockade and immunogenic chemotherapy for effective chemoimmunotherapy
title_full_unstemmed Dual-responsive nanosystem based on TGF-β blockade and immunogenic chemotherapy for effective chemoimmunotherapy
title_short Dual-responsive nanosystem based on TGF-β blockade and immunogenic chemotherapy for effective chemoimmunotherapy
title_sort dual-responsive nanosystem based on tgf-β blockade and immunogenic chemotherapy for effective chemoimmunotherapy
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090387/
https://www.ncbi.nlm.nih.gov/pubmed/35506467
http://dx.doi.org/10.1080/10717544.2022.2069877
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