基于β-环糊精纳米凝胶载体系统的抗pd - l1和吲哚菁绿共递送用于癌症靶向光热和免疫治疗。

IF 5.4 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xichuan Tang, Yuting Wen, Zhongxing Zhang, Xia Song, Jingling Zhu, Minjie Zheng, Jun Li
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引用次数: 0

摘要

程序性死亡配体1 (PD-L1)是一种免疫检查点蛋白,作为“不要吃我”的信号,允许癌细胞逃避免疫系统的检测和清除。用PD-L1抗体(aPD-L1)阻断PD-L1可恢复免疫。同时,光热疗法(PTT)诱导局部肿瘤细胞死亡并释放损伤相关分子模式(DAMPs),进一步刺激免疫反应。在这里,我们开发了一种多功能纳米凝胶系统,由β-环糊精(β-CD),聚乙烯亚胺(PEI)和聚乙二醇(PEG)组成,被称为CPP纳米凝胶,设计用于共递送aPD-L1和吲哚菁绿(ICG), PTT光敏剂。β-CD部分通过宿主-客体相互作用促进ICG加载,而PEI使aPD-L1偶联。靶向肿瘤细胞后,纳米凝胶阻断PD-L1,并在808 nm激光照射下触发ptt诱导的DAMPs释放。通过促进热诱导的细胞死亡和免疫反应,多功能CPP纳米凝胶代表了一种有潜力的治疗局部和转移性癌症的系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Codelivery of Anti-PD-L1 and Indocyanine Green by a β-Cyclodextrin-Based Nanogel Carrier System for Cancer-Targeted Photothermal and Immunotherapy.

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.

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来源期刊
Biomacromolecules
Biomacromolecules 化学-高分子科学
CiteScore
10.60
自引率
4.80%
发文量
417
审稿时长
1.6 months
期刊介绍: Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine. Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.
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