Sulfate Radical Based In Situ Vaccine Boosts Systemic Antitumor Immunity via Concurrent Activation of Necroptosis and STING Pathway

© 2024 Wiley‐VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 36(2024), 41 vom: 16. Okt., Seite e2407914
1. Verfasser: Huang, Yiming (VerfasserIn)
Weitere Verfasser: Zou, Jie, Huo, Jiangyan, Zhang, Min, Yang, Yannan
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article immunogenic cancer cell death in situ vaccine layered double hydroxide sulfate radicals Cancer Vaccines Sulfates Membrane Proteins Manganese 42Z2K6ZL8P
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520 |a In situ vaccine (ISV) can provoke systemic anti-tumor immunity through the induction of immunogenic cell death (ICD). The development of ISV technology has been restricted by the limited and suboptimal ICD driven tumor antigen production which are currently relying on chemo-drugs, photo-/radio-sensitizers, oncolytic-virus and immunostimulatory agents. Herein, a sulfate radical (SO4 ·-) based ISV is reported that accomplishes superior tumor immunotherapy dispense from conventional approaches. The ISV denoted as P-Mn-LDH is constructed by intercalating peroxydisulfate (PDS, a precursor of SO4 ·-) into manganese layered double hydroxide nanoparticles (Mn-LDH). This design allows the stabilization of PDS under ambient condition, but triggers a Mn2+ mediated PDS decomposition in acidic tumor microenvironment (TME) to generate in situ SO4 ·-. Importantly, it is found that the SO4 ·- radicals not only effectively kill cancer cells, but also induce a necroptotic cell death pathway, leading to robust ICD signaling for eliciting adaptive immunity. Further, the P-Mn-LDH can activate the stimulator of interferon genes (STING) pathway to further boost anti-tumor immunity. Collectively, the P-Mn-LDH based ISV exhibited potent activity in inhibiting tumor growth and lung metastasis. When combined with immune checkpoint inhibitor, significant inhibition of distant tumors is achieved. This study underpins the promise of SO4 ·- based vaccine technology for cancer immunotherapy 
650 4 |a Journal Article 
650 4 |a immunogenic cancer cell death 
650 4 |a in situ vaccine 
650 4 |a layered double hydroxide 
650 4 |a sulfate radicals 
650 7 |a Cancer Vaccines  |2 NLM 
650 7 |a Sulfates  |2 NLM 
650 7 |a Membrane Proteins  |2 NLM 
650 7 |a Manganese  |2 NLM 
650 7 |a 42Z2K6ZL8P  |2 NLM 
700 1 |a Zou, Jie  |e verfasserin  |4 aut 
700 1 |a Huo, Jiangyan  |e verfasserin  |4 aut 
700 1 |a Zhang, Min  |e verfasserin  |4 aut 
700 1 |a Yang, Yannan  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Advanced materials (Deerfield Beach, Fla.)  |d 1998  |g 36(2024), 41 vom: 16. Okt., Seite e2407914  |w (DE-627)NLM098206397  |x 1521-4095  |7 nnas 
773 1 8 |g volume:36  |g year:2024  |g number:41  |g day:16  |g month:10  |g pages:e2407914 
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