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Engineering CpG-ASO-Pt-Loaded Macrophages (CAP@M) for Synergistic Chemo-/Gene-/Immuno-Therapy

Adoptive cell therapy by natural cells for drug delivery has achieved encouraging progress in cancer treatment over small-molecule drugs. Macrophages have a great potential in antitumor drug delivery due to their innate capability of sensing chemotactic cues and homing toward tumors. However, major...

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Autores principales: Wang, Yuqi, Zhang, Lingpu, Liu, Yan, Tang, Linlin, He, Juan, Sun, Xiaqing, Younis, Muhsin H., Cui, Daxiang, Xiao, Haihua, Gao, Dong, Kong, Xiang-Yang, Cai, Weibo, Song, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664705/
https://www.ncbi.nlm.nih.gov/pubmed/35668035
http://dx.doi.org/10.1002/adhm.202201178
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author Wang, Yuqi
Zhang, Lingpu
Liu, Yan
Tang, Linlin
He, Juan
Sun, Xiaqing
Younis, Muhsin H.
Cui, Daxiang
Xiao, Haihua
Gao, Dong
Kong, Xiang-Yang
Cai, Weibo
Song, Jie
author_facet Wang, Yuqi
Zhang, Lingpu
Liu, Yan
Tang, Linlin
He, Juan
Sun, Xiaqing
Younis, Muhsin H.
Cui, Daxiang
Xiao, Haihua
Gao, Dong
Kong, Xiang-Yang
Cai, Weibo
Song, Jie
author_sort Wang, Yuqi
collection PubMed
description Adoptive cell therapy by natural cells for drug delivery has achieved encouraging progress in cancer treatment over small-molecule drugs. Macrophages have a great potential in antitumor drug delivery due to their innate capability of sensing chemotactic cues and homing toward tumors. However, major challenge in current macrophage-based cell therapy is loading macrophages with adequate amounts of therapeutic, while allowing them to play a role in immunity without compromising cell functions. Herein, a potent strategy to construct a macrophage-mediated drug delivery platform loaded with a nanosphere (CpG-ASO-Pt) (CAP) composed of functional nucleic acid therapeutic (CpG-ASO) and chemotherapeutic drug cisplatin (Pt) is demonstrated. These CAP nanosphere loaded macrophages (CAP@M) are employed not only as carriers to deliver this nanosphere toward the tumor sites, but also simultaneously to guide the differentiation and maintain immunostimulatory effects. Both in vitro and in vivo experiments indicate that CAP@M is a promising nanomedicine by macrophage-mediated nanospheres delivery and synergistically immunostimulatory activities. Taken together, this study provides a new strategy to construct a macrophage-based drug delivery system for synergistic chemo-/gene-/immuno-therapy.
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spelling pubmed-96647052022-11-14 Engineering CpG-ASO-Pt-Loaded Macrophages (CAP@M) for Synergistic Chemo-/Gene-/Immuno-Therapy Wang, Yuqi Zhang, Lingpu Liu, Yan Tang, Linlin He, Juan Sun, Xiaqing Younis, Muhsin H. Cui, Daxiang Xiao, Haihua Gao, Dong Kong, Xiang-Yang Cai, Weibo Song, Jie Adv Healthc Mater Article Adoptive cell therapy by natural cells for drug delivery has achieved encouraging progress in cancer treatment over small-molecule drugs. Macrophages have a great potential in antitumor drug delivery due to their innate capability of sensing chemotactic cues and homing toward tumors. However, major challenge in current macrophage-based cell therapy is loading macrophages with adequate amounts of therapeutic, while allowing them to play a role in immunity without compromising cell functions. Herein, a potent strategy to construct a macrophage-mediated drug delivery platform loaded with a nanosphere (CpG-ASO-Pt) (CAP) composed of functional nucleic acid therapeutic (CpG-ASO) and chemotherapeutic drug cisplatin (Pt) is demonstrated. These CAP nanosphere loaded macrophages (CAP@M) are employed not only as carriers to deliver this nanosphere toward the tumor sites, but also simultaneously to guide the differentiation and maintain immunostimulatory effects. Both in vitro and in vivo experiments indicate that CAP@M is a promising nanomedicine by macrophage-mediated nanospheres delivery and synergistically immunostimulatory activities. Taken together, this study provides a new strategy to construct a macrophage-based drug delivery system for synergistic chemo-/gene-/immuno-therapy. 2022-08 2022-06-19 /pmc/articles/PMC9664705/ /pubmed/35668035 http://dx.doi.org/10.1002/adhm.202201178 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Article
Wang, Yuqi
Zhang, Lingpu
Liu, Yan
Tang, Linlin
He, Juan
Sun, Xiaqing
Younis, Muhsin H.
Cui, Daxiang
Xiao, Haihua
Gao, Dong
Kong, Xiang-Yang
Cai, Weibo
Song, Jie
Engineering CpG-ASO-Pt-Loaded Macrophages (CAP@M) for Synergistic Chemo-/Gene-/Immuno-Therapy
title Engineering CpG-ASO-Pt-Loaded Macrophages (CAP@M) for Synergistic Chemo-/Gene-/Immuno-Therapy
title_full Engineering CpG-ASO-Pt-Loaded Macrophages (CAP@M) for Synergistic Chemo-/Gene-/Immuno-Therapy
title_fullStr Engineering CpG-ASO-Pt-Loaded Macrophages (CAP@M) for Synergistic Chemo-/Gene-/Immuno-Therapy
title_full_unstemmed Engineering CpG-ASO-Pt-Loaded Macrophages (CAP@M) for Synergistic Chemo-/Gene-/Immuno-Therapy
title_short Engineering CpG-ASO-Pt-Loaded Macrophages (CAP@M) for Synergistic Chemo-/Gene-/Immuno-Therapy
title_sort engineering cpg-aso-pt-loaded macrophages (cap@m) for synergistic chemo-/gene-/immuno-therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664705/
https://www.ncbi.nlm.nih.gov/pubmed/35668035
http://dx.doi.org/10.1002/adhm.202201178
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