Codelivery of Anti-PD-L1 and Indocyanine Green by a β-Cyclodextrin-Based Nanogel Carrier System for Cancer-Targeted Photothermal and Immunotherapy.
1/5 보강
Programmed death-ligand 1 (PD-L1), an immune checkpoint protein, serves as a "don't eat me" signal that allows cancer cells to evade detection and clearance by the immune system.
APA
Tang X, Wen Y, et al. (2025). Codelivery of Anti-PD-L1 and Indocyanine Green by a β-Cyclodextrin-Based Nanogel Carrier System for Cancer-Targeted Photothermal and Immunotherapy.. Biomacromolecules, 26(12), 8345-8357. https://doi.org/10.1021/acs.biomac.5c00489
MLA
Tang X, et al.. "Codelivery of Anti-PD-L1 and Indocyanine Green by a β-Cyclodextrin-Based Nanogel Carrier System for Cancer-Targeted Photothermal and Immunotherapy.." Biomacromolecules, vol. 26, no. 12, 2025, pp. 8345-8357.
PMID
40499082
Abstract
Programmed death-ligand 1 (PD-L1), an immune checkpoint protein, serves as a "don't eat me" signal that allows cancer cells to evade detection and clearance by the immune system. Blocking PD-L1 with the PD-L1 antibody (aPD-L1) can restore the immunity. Photothermal therapy (PTT), meanwhile, induces local tumor cell death and releases damage-associated molecular patterns (DAMPs) to further stimulate immune responses. Here, we developed a multifunctional nanogel system, composed of β-cyclodextrin (β-CD), polyethylenimine (PEI), and polyethylene glycol (PEG), referred to as CPP nanogels, designed for the codelivery of aPD-L1 and indocyanine green (ICG), a PTT photosensitizer. The β-CD moieties facilitated ICG loading through host-guest interactions, while PEI enabled aPD-L1 conjugation. Upon targeting tumor cells, the nanogels blocked PD-L1 and, under 808 nm laser irradiation, triggered PTT-induced DAMPs release. By promoting both heat-induced cell death and immune responses, the multifunctional CPP nanogels represent a promising system potentially for treating localized and metastatic cancers.
🏷️ 키워드 / MeSH
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