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An injectable signal-amplifying device elicits a specific immune response against malignant glioblastoma

Despite exciting achievements with some malignancies, immunotherapy for hypoimmunogenic cancers, especially glioblastoma (GBM), remains a formidable clinical challenge. Poor immunogenicity and deficient immune infiltrates are two major limitations to an effective cancer-specific immune response. Her...

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Autores principales: Qiu, Qiujun, Chen, Sunhui, He, Huining, Chen, Jixiang, Ding, Xinyi, Wang, Dongdong, Yang, Jiangang, Guo, Pengcheng, Li, Yang, Kim, Jisu, Sheng, Jianyong, Gao, Chao, Yin, Bo, Zheng, Shihao, Wang, Jianxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10692361/
https://www.ncbi.nlm.nih.gov/pubmed/38045037
http://dx.doi.org/10.1016/j.apsb.2023.06.010
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author Qiu, Qiujun
Chen, Sunhui
He, Huining
Chen, Jixiang
Ding, Xinyi
Wang, Dongdong
Yang, Jiangang
Guo, Pengcheng
Li, Yang
Kim, Jisu
Sheng, Jianyong
Gao, Chao
Yin, Bo
Zheng, Shihao
Wang, Jianxin
author_facet Qiu, Qiujun
Chen, Sunhui
He, Huining
Chen, Jixiang
Ding, Xinyi
Wang, Dongdong
Yang, Jiangang
Guo, Pengcheng
Li, Yang
Kim, Jisu
Sheng, Jianyong
Gao, Chao
Yin, Bo
Zheng, Shihao
Wang, Jianxin
author_sort Qiu, Qiujun
collection PubMed
description Despite exciting achievements with some malignancies, immunotherapy for hypoimmunogenic cancers, especially glioblastoma (GBM), remains a formidable clinical challenge. Poor immunogenicity and deficient immune infiltrates are two major limitations to an effective cancer-specific immune response. Herein, we propose that an injectable signal-amplifying nanocomposite/hydrogel system consisting of granulocyte-macrophage colony-stimulating factor and imiquimod-loaded antigen-capturing nanoparticles can simultaneously amplify the chemotactic signal of antigen-presenting cells and the “danger” signal of GBM. We demonstrated the feasibility of this strategy in two scenarios of GBM. In the first scenario, we showed that this simultaneous amplification system, in conjunction with local chemotherapy, enhanced both the immunogenicity and immune infiltrates in a recurrent GBM model; thus, ultimately making a cold GBM hot and suppressing postoperative relapse. Encouraged by excellent efficacy, we further exploited this signal-amplifying system to improve the efficiency of vaccine lysate in the treatment of refractory multiple GBM, a disease with limited clinical treatment options. In general, this biomaterial-based immune signal amplification system represents a unique approach to restore GBM-specific immunity and may provide a beneficial preliminary treatment for other clinically refractory malignancies.
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spelling pubmed-106923612023-12-03 An injectable signal-amplifying device elicits a specific immune response against malignant glioblastoma Qiu, Qiujun Chen, Sunhui He, Huining Chen, Jixiang Ding, Xinyi Wang, Dongdong Yang, Jiangang Guo, Pengcheng Li, Yang Kim, Jisu Sheng, Jianyong Gao, Chao Yin, Bo Zheng, Shihao Wang, Jianxin Acta Pharm Sin B Original Article Despite exciting achievements with some malignancies, immunotherapy for hypoimmunogenic cancers, especially glioblastoma (GBM), remains a formidable clinical challenge. Poor immunogenicity and deficient immune infiltrates are two major limitations to an effective cancer-specific immune response. Herein, we propose that an injectable signal-amplifying nanocomposite/hydrogel system consisting of granulocyte-macrophage colony-stimulating factor and imiquimod-loaded antigen-capturing nanoparticles can simultaneously amplify the chemotactic signal of antigen-presenting cells and the “danger” signal of GBM. We demonstrated the feasibility of this strategy in two scenarios of GBM. In the first scenario, we showed that this simultaneous amplification system, in conjunction with local chemotherapy, enhanced both the immunogenicity and immune infiltrates in a recurrent GBM model; thus, ultimately making a cold GBM hot and suppressing postoperative relapse. Encouraged by excellent efficacy, we further exploited this signal-amplifying system to improve the efficiency of vaccine lysate in the treatment of refractory multiple GBM, a disease with limited clinical treatment options. In general, this biomaterial-based immune signal amplification system represents a unique approach to restore GBM-specific immunity and may provide a beneficial preliminary treatment for other clinically refractory malignancies. Elsevier 2023-12 2023-06-20 /pmc/articles/PMC10692361/ /pubmed/38045037 http://dx.doi.org/10.1016/j.apsb.2023.06.010 Text en © 2023 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Qiu, Qiujun
Chen, Sunhui
He, Huining
Chen, Jixiang
Ding, Xinyi
Wang, Dongdong
Yang, Jiangang
Guo, Pengcheng
Li, Yang
Kim, Jisu
Sheng, Jianyong
Gao, Chao
Yin, Bo
Zheng, Shihao
Wang, Jianxin
An injectable signal-amplifying device elicits a specific immune response against malignant glioblastoma
title An injectable signal-amplifying device elicits a specific immune response against malignant glioblastoma
title_full An injectable signal-amplifying device elicits a specific immune response against malignant glioblastoma
title_fullStr An injectable signal-amplifying device elicits a specific immune response against malignant glioblastoma
title_full_unstemmed An injectable signal-amplifying device elicits a specific immune response against malignant glioblastoma
title_short An injectable signal-amplifying device elicits a specific immune response against malignant glioblastoma
title_sort injectable signal-amplifying device elicits a specific immune response against malignant glioblastoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10692361/
https://www.ncbi.nlm.nih.gov/pubmed/38045037
http://dx.doi.org/10.1016/j.apsb.2023.06.010
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