Activating Iterative Revolutions of the Cancer-Immunity Cycle in Hypoxic Tumors with a Smart Nano-Regulator

© 2024 Wiley‐VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 36(2024), 29 vom: 09. Juli, Seite e2400196
1. Verfasser: Ding, Junying (VerfasserIn)
Weitere Verfasser: Lu, Yang, Zhao, Xueze, Long, Saran, Du, Jianjun, Sun, Wen, Fan, Jiangli, Peng, Xiaojun
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article activatable nano‐regulator cancer immunity cycle hypoxic tumor therapy immune resistance Photosensitizing Agents Triazoles (+)-JQ1 compound Azepines Polyethylene Glycols mehr... 3WJQ0SDW1A B7-H1 Antigen
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520 |a The activation of sequential events in the cancer-immunity cycle (CIC) is crucial for achieving effective antitumor immunity. However, formidable challenges, such as innate and adaptive immune resistance, along with the off-target adverse effects of nonselective immunomodulators, persist. In this study, a tumor-selective nano-regulator named PNBJQ has been presented, focusing on targeting two nonredundant immune nodes: inducing immunogenic cancer cell death and abrogating immune resistance to fully activate endogenous tumor immunity. PNBJQ is obtained by encapsulating the immunomodulating agent JQ1 within a self-assembling system formed by linking a Type-I photosensitizer to polyethylene glycol through a hypoxia-sensitive azo bond. Benefiting from the Type-I photosensitive mechanism, PNBJQ triggers the immunogenic cell death of hypoxic tumors under near-infrared (NIR) light irradiation. This process resolves innate immune resistance by stimulating sufficient cytotoxic T-lymphocytes. Simultaneously, PNBJQ smartly responds to the hypoxic tumor microenvironment for precise drug delivery, adeptly addressing adaptive immune resistance by using JQ1 to downregulate programmed death ligand 1 (PD-L1) and sustaining the response of cytotoxic T lymphocytes. The activatable synergic photoimmunotherapy promotes an immune-promoting tumor microenvironment by activating an iterative revolution of the CIC, which remarkably eradicates established hypoxic tumors and suppresses distal lesions under low light dose irradiation 
650 4 |a Journal Article 
650 4 |a activatable nano‐regulator 
650 4 |a cancer immunity cycle 
650 4 |a hypoxic tumor therapy 
650 4 |a immune resistance 
650 7 |a Photosensitizing Agents  |2 NLM 
650 7 |a Triazoles  |2 NLM 
650 7 |a (+)-JQ1 compound  |2 NLM 
650 7 |a Azepines  |2 NLM 
650 7 |a Polyethylene Glycols  |2 NLM 
650 7 |a 3WJQ0SDW1A  |2 NLM 
650 7 |a B7-H1 Antigen  |2 NLM 
700 1 |a Lu, Yang  |e verfasserin  |4 aut 
700 1 |a Zhao, Xueze  |e verfasserin  |4 aut 
700 1 |a Long, Saran  |e verfasserin  |4 aut 
700 1 |a Du, Jianjun  |e verfasserin  |4 aut 
700 1 |a Sun, Wen  |e verfasserin  |4 aut 
700 1 |a Fan, Jiangli  |e verfasserin  |4 aut 
700 1 |a Peng, Xiaojun  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Advanced materials (Deerfield Beach, Fla.)  |d 1998  |g 36(2024), 29 vom: 09. Juli, Seite e2400196  |w (DE-627)NLM098206397  |x 1521-4095  |7 nnns 
773 1 8 |g volume:36  |g year:2024  |g number:29  |g day:09  |g month:07  |g pages:e2400196 
856 4 0 |u http://dx.doi.org/10.1002/adma.202400196  |3 Volltext 
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