Activable Nano-Immunomodulator Assembled from π-Extended Naphthalenediimide for Precision Photothermal Immunotherapy
© 2024 Wiley‐VCH GmbH..
A nano-immunomodulator (R-NPT NP) comprising a tumor microenvironment (TME) activable resiquimod (R848) and a π-extended NIR-absorbing naphthophenanthrolinetetraone (NPT) has been engineered for spatiotemporal controlled photothermal immunotherapy. R-NPT NP demonstrated excellent photostability, while R848 promoted synergistic immunity as a toll-like receptor 7/8 (TLR7/8) agonist. Upon accumulation at the tumor site, R-NPT NP released R848 in response to redox metabolite glutathione (GSH), triggering dendritic cell (DC) activation. The photothermal effect endowed by R-NPT NP can ablate tumors directly and trigger immunogenic cell death to augment immunity after photoirradiation. The synergistic effect of GSH-liable TLR7/8 agonist and released immunogenic factors leads to a robust evocation of systematic immunity through promoted DC maturation and T cell infiltration. Thus, R-NPT NP with photoirradiation achieved 99.3% and 98.2% growth inhibition against primary and distal tumors, respectively.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2024 |
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Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - year:2024 |
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Enthalten in: |
Angewandte Chemie (International ed. in English) - (2024) vom: 04. Apr., Seite e202401250 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Zhong, Wenbin [VerfasserIn] |
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Links: |
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Themen: |
J-aggregation, π-extended naphthalenediimide, glutathione activable effect, organic assembly, photothermal immunotherapy |
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Anmerkungen: |
Date Revised 05.04.2024 published: Print-Electronic Citation Status Publisher |
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doi: |
10.1002/anie.202401250 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM370656695 |
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520 | |a A nano-immunomodulator (R-NPT NP) comprising a tumor microenvironment (TME) activable resiquimod (R848) and a π-extended NIR-absorbing naphthophenanthrolinetetraone (NPT) has been engineered for spatiotemporal controlled photothermal immunotherapy. R-NPT NP demonstrated excellent photostability, while R848 promoted synergistic immunity as a toll-like receptor 7/8 (TLR7/8) agonist. Upon accumulation at the tumor site, R-NPT NP released R848 in response to redox metabolite glutathione (GSH), triggering dendritic cell (DC) activation. The photothermal effect endowed by R-NPT NP can ablate tumors directly and trigger immunogenic cell death to augment immunity after photoirradiation. The synergistic effect of GSH-liable TLR7/8 agonist and released immunogenic factors leads to a robust evocation of systematic immunity through promoted DC maturation and T cell infiltration. Thus, R-NPT NP with photoirradiation achieved 99.3% and 98.2% growth inhibition against primary and distal tumors, respectively | ||
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700 | 1 | |a Chen, Yun |e verfasserin |4 aut | |
700 | 1 | |a Ma, Zhaoyu |e verfasserin |4 aut | |
700 | 1 | |a Ma, Mengmeng |e verfasserin |4 aut | |
700 | 1 | |a Tan, Brynne Shu Ni |e verfasserin |4 aut | |
700 | 1 | |a Yang, Jie |e verfasserin |4 aut | |
700 | 1 | |a Zhao, Yanli |e verfasserin |4 aut | |
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