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Modular Hydrogel Vaccine for Programmable and Coordinate Elicitation of Cancer Immunotherapy

Immunotherapy holds great promise for the treatment of malignant cancer. However, the lack of sufficient tumor neoantigens and incomplete dendritic cell (DC) maturation compromise the efficacy of immunotherapy. Here, a modular hydrogel‐based vaccine capable of eliciting a powerful and sustained immu...

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Autores principales: Ji, Panpan, Sun, Wenqi, Zhang, Siyan, Xing, Yuqi, Wang, Chen, Wei, Mengying, Li, Qiuyun, Ji, Gang, Yang, Guodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401092/
https://www.ncbi.nlm.nih.gov/pubmed/37222047
http://dx.doi.org/10.1002/advs.202301789
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author Ji, Panpan
Sun, Wenqi
Zhang, Siyan
Xing, Yuqi
Wang, Chen
Wei, Mengying
Li, Qiuyun
Ji, Gang
Yang, Guodong
author_facet Ji, Panpan
Sun, Wenqi
Zhang, Siyan
Xing, Yuqi
Wang, Chen
Wei, Mengying
Li, Qiuyun
Ji, Gang
Yang, Guodong
author_sort Ji, Panpan
collection PubMed
description Immunotherapy holds great promise for the treatment of malignant cancer. However, the lack of sufficient tumor neoantigens and incomplete dendritic cell (DC) maturation compromise the efficacy of immunotherapy. Here, a modular hydrogel‐based vaccine capable of eliciting a powerful and sustained immune response is developed. Briefly, CCL21a and Exo(GM‐CSF+Ce6) (tumor cell‐derived exosomes with granulocyte‐macrophage colony‐stimulating factor (GM‐CSF) mRNA encapsulated inside and sonosensitizer chlorin e6 (Ce6) incorporated in the surface) are mixed with nanoclay and gelatin methacryloyl, forming the hydrogel designated as CCL21a/Exo(GM‐CSF+Ce6)@nanoGel. The engineered hydrogel releases CCL21a and GM‐CSF with a time gap. The earlier released CCL21a diverts the tumor‐draining lymph node (TdLN) metastatic tumor cells to the hydrogel. Consequently, the trapped tumor cells in the hydrogel, in turn, engulf the Ce6‐containing exosomes and thus are eradicated by sonodynamic therapy (SDT), serving as the antigen source. Later, together with the remnant CCL21a, GM‐CSF produced by cells engulfing Exo(GM‐CSF+Ce6) continuously recruits and provokes DCs. With the two programmed modules, the engineered modular hydrogel vaccine efficiently inhibits tumor growth and metastasis via diverting TdLN metastatic cancer to hydrogel, killing the trapped tumor cells, and eliciting prolonged and powerful immunotherapy in an orchestrated manner. The strategy would open an avenue for cancer immunotherapy.
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spelling pubmed-104010922023-08-05 Modular Hydrogel Vaccine for Programmable and Coordinate Elicitation of Cancer Immunotherapy Ji, Panpan Sun, Wenqi Zhang, Siyan Xing, Yuqi Wang, Chen Wei, Mengying Li, Qiuyun Ji, Gang Yang, Guodong Adv Sci (Weinh) Research Articles Immunotherapy holds great promise for the treatment of malignant cancer. However, the lack of sufficient tumor neoantigens and incomplete dendritic cell (DC) maturation compromise the efficacy of immunotherapy. Here, a modular hydrogel‐based vaccine capable of eliciting a powerful and sustained immune response is developed. Briefly, CCL21a and Exo(GM‐CSF+Ce6) (tumor cell‐derived exosomes with granulocyte‐macrophage colony‐stimulating factor (GM‐CSF) mRNA encapsulated inside and sonosensitizer chlorin e6 (Ce6) incorporated in the surface) are mixed with nanoclay and gelatin methacryloyl, forming the hydrogel designated as CCL21a/Exo(GM‐CSF+Ce6)@nanoGel. The engineered hydrogel releases CCL21a and GM‐CSF with a time gap. The earlier released CCL21a diverts the tumor‐draining lymph node (TdLN) metastatic tumor cells to the hydrogel. Consequently, the trapped tumor cells in the hydrogel, in turn, engulf the Ce6‐containing exosomes and thus are eradicated by sonodynamic therapy (SDT), serving as the antigen source. Later, together with the remnant CCL21a, GM‐CSF produced by cells engulfing Exo(GM‐CSF+Ce6) continuously recruits and provokes DCs. With the two programmed modules, the engineered modular hydrogel vaccine efficiently inhibits tumor growth and metastasis via diverting TdLN metastatic cancer to hydrogel, killing the trapped tumor cells, and eliciting prolonged and powerful immunotherapy in an orchestrated manner. The strategy would open an avenue for cancer immunotherapy. John Wiley and Sons Inc. 2023-05-24 /pmc/articles/PMC10401092/ /pubmed/37222047 http://dx.doi.org/10.1002/advs.202301789 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Ji, Panpan
Sun, Wenqi
Zhang, Siyan
Xing, Yuqi
Wang, Chen
Wei, Mengying
Li, Qiuyun
Ji, Gang
Yang, Guodong
Modular Hydrogel Vaccine for Programmable and Coordinate Elicitation of Cancer Immunotherapy
title Modular Hydrogel Vaccine for Programmable and Coordinate Elicitation of Cancer Immunotherapy
title_full Modular Hydrogel Vaccine for Programmable and Coordinate Elicitation of Cancer Immunotherapy
title_fullStr Modular Hydrogel Vaccine for Programmable and Coordinate Elicitation of Cancer Immunotherapy
title_full_unstemmed Modular Hydrogel Vaccine for Programmable and Coordinate Elicitation of Cancer Immunotherapy
title_short Modular Hydrogel Vaccine for Programmable and Coordinate Elicitation of Cancer Immunotherapy
title_sort modular hydrogel vaccine for programmable and coordinate elicitation of cancer immunotherapy
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401092/
https://www.ncbi.nlm.nih.gov/pubmed/37222047
http://dx.doi.org/10.1002/advs.202301789
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