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pH-gated nanoparticles selectively regulate lysosomal function of tumour-associated macrophages for cancer immunotherapy

Tumour-associated macrophages (TAMs), as one of the most abundant tumour-infiltrating immune cells, play a pivotal role in tumour antigen clearance and immune suppression. M2-like TAMs present a heightened lysosomal acidity and protease activity, limiting an effective antigen cross-presentation. How...

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Autores principales: Tang, Mingmei, Chen, Binlong, Xia, Heming, Pan, Meijie, Zhao, Ruiyang, Zhou, Jiayi, Yin, Qingqing, Wan, Fangjie, Yan, Yue, Fu, Chuanxun, Zhong, Lijun, Zhang, Qiang, Wang, Yiguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514266/
https://www.ncbi.nlm.nih.gov/pubmed/37735462
http://dx.doi.org/10.1038/s41467-023-41592-0
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author Tang, Mingmei
Chen, Binlong
Xia, Heming
Pan, Meijie
Zhao, Ruiyang
Zhou, Jiayi
Yin, Qingqing
Wan, Fangjie
Yan, Yue
Fu, Chuanxun
Zhong, Lijun
Zhang, Qiang
Wang, Yiguang
author_facet Tang, Mingmei
Chen, Binlong
Xia, Heming
Pan, Meijie
Zhao, Ruiyang
Zhou, Jiayi
Yin, Qingqing
Wan, Fangjie
Yan, Yue
Fu, Chuanxun
Zhong, Lijun
Zhang, Qiang
Wang, Yiguang
author_sort Tang, Mingmei
collection PubMed
description Tumour-associated macrophages (TAMs), as one of the most abundant tumour-infiltrating immune cells, play a pivotal role in tumour antigen clearance and immune suppression. M2-like TAMs present a heightened lysosomal acidity and protease activity, limiting an effective antigen cross-presentation. How to selectively reprogram M2-like TAMs to reinvigorate anti-tumour immune responses is challenging. Here, we report a pH-gated nanoadjuvant (PGN) that selectively targets the lysosomes of M2-like TAMs in tumours rather than the corresponding organelles from macrophages in healthy tissues. Enabled by the PGN nanotechnology, M2-like TAMs are specifically switched to a M1-like phenotype with attenuated lysosomal acidity and cathepsin activity for improved antigen cross-presentation, thus eliciting adaptive immune response and sustained tumour regression in tumour-bearing female mice. Our findings provide insights into how to specifically regulate lysosomal function of TAMs for efficient cancer immunotherapy.
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spelling pubmed-105142662023-09-23 pH-gated nanoparticles selectively regulate lysosomal function of tumour-associated macrophages for cancer immunotherapy Tang, Mingmei Chen, Binlong Xia, Heming Pan, Meijie Zhao, Ruiyang Zhou, Jiayi Yin, Qingqing Wan, Fangjie Yan, Yue Fu, Chuanxun Zhong, Lijun Zhang, Qiang Wang, Yiguang Nat Commun Article Tumour-associated macrophages (TAMs), as one of the most abundant tumour-infiltrating immune cells, play a pivotal role in tumour antigen clearance and immune suppression. M2-like TAMs present a heightened lysosomal acidity and protease activity, limiting an effective antigen cross-presentation. How to selectively reprogram M2-like TAMs to reinvigorate anti-tumour immune responses is challenging. Here, we report a pH-gated nanoadjuvant (PGN) that selectively targets the lysosomes of M2-like TAMs in tumours rather than the corresponding organelles from macrophages in healthy tissues. Enabled by the PGN nanotechnology, M2-like TAMs are specifically switched to a M1-like phenotype with attenuated lysosomal acidity and cathepsin activity for improved antigen cross-presentation, thus eliciting adaptive immune response and sustained tumour regression in tumour-bearing female mice. Our findings provide insights into how to specifically regulate lysosomal function of TAMs for efficient cancer immunotherapy. Nature Publishing Group UK 2023-09-21 /pmc/articles/PMC10514266/ /pubmed/37735462 http://dx.doi.org/10.1038/s41467-023-41592-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tang, Mingmei
Chen, Binlong
Xia, Heming
Pan, Meijie
Zhao, Ruiyang
Zhou, Jiayi
Yin, Qingqing
Wan, Fangjie
Yan, Yue
Fu, Chuanxun
Zhong, Lijun
Zhang, Qiang
Wang, Yiguang
pH-gated nanoparticles selectively regulate lysosomal function of tumour-associated macrophages for cancer immunotherapy
title pH-gated nanoparticles selectively regulate lysosomal function of tumour-associated macrophages for cancer immunotherapy
title_full pH-gated nanoparticles selectively regulate lysosomal function of tumour-associated macrophages for cancer immunotherapy
title_fullStr pH-gated nanoparticles selectively regulate lysosomal function of tumour-associated macrophages for cancer immunotherapy
title_full_unstemmed pH-gated nanoparticles selectively regulate lysosomal function of tumour-associated macrophages for cancer immunotherapy
title_short pH-gated nanoparticles selectively regulate lysosomal function of tumour-associated macrophages for cancer immunotherapy
title_sort ph-gated nanoparticles selectively regulate lysosomal function of tumour-associated macrophages for cancer immunotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514266/
https://www.ncbi.nlm.nih.gov/pubmed/37735462
http://dx.doi.org/10.1038/s41467-023-41592-0
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