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核心技术专利:CN118964589B侵权必究
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Accurately Controlled Tumor Temperature with Silica-Coated Gold Nanorods for Optimal Immune Checkpoint Blockade Therapy.

作者信息

Yun Wan Su, Yang Wonseok, Shim Man Kyu, Song Sukyung, Choi Jiwoong, Kim Jeongrae, Kim Jinseong, Moon Yujeong, Jo SeongHoon, Lim Dong-Kwon, Kim Kwangmeyung

机构信息

College of Pharmacy, Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, Republic of Korea.

KU-KIST Graduate School of Converging Science and Technology, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, Republic of Korea.

出版信息

Biomater Res. 2024 Apr 29;28:0024. doi: 10.34133/bmr.0024. eCollection 2024.


DOI:10.34133/bmr.0024
PMID:38694230
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11062504/
Abstract

Photothermal therapy (PTT) at mild temperatures ranging from 44 to 45 °C holds tremendous promise as a strategy for inducing potent immunogenic cell death (ICD) within tumor tissues, which can reverse the immunosuppressive tumor microenvironment (ITM) into an immune-responsive milieu. However, accurately and precisely controlling the tumor temperature remains a formidable challenge. Here, we report the precision photothermal immunotherapy by using silica-coated gold nanorods (AuNR@SiO), and investigating the optimal administration routes and treatment protocols, which enabled to achieve the sustained and controlled mild heating within the tumor tissues. First, the highest photothermal performance of AuNR@SiO with 20-nm silica shell thickness than 5 or 40 nm was confirmed in vitro and in vivo. Then, the optimal conditions for precision immunotherapy were further investigated to produce mild temperature (44 to 45 °C) accurately in tumor tissues. The optimal conditions with AuNR@SiO result in a distinct cell death with high early/late apoptosis and low necrosis, leading to very efficient ICD compared to lower or higher temperatures. In colon tumor-bearing mice, intratumorally injected AuNR@SiO efficiently promotes a mild temperature within the tumor tissues by local irradiation of near-infrared (NIR) laser. This mild PTT substantially increases the population of mature dendritic cells (DCs) and cytotoxic T cells (CTLs) within tumor tissues, ultimately reversing the ITM into an immune-responsive milieu. Furthermore, we found that the combination mild PTT with AuNR@SiO and anti-PD-L1 therapy could lead to the 100% complete regression of primary tumors and immunological memory to prevent tumor recurrence. Collectively, this study demonstrates that AuNR@SiO with a robust methodology capable of continuously inducing mild temperature accurately within the ITM holds promise as an approach to achieve the precision photothermal immunotherapy.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/7a0f6a4d570d/bmr.0024.fig.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/d2928e648c6d/bmr.0024.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/981ad034b0cb/bmr.0024.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/b3079ff40425/bmr.0024.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/a46c05426cbe/bmr.0024.fig.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/3e4a289e3ae3/bmr.0024.fig.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/7a0f6a4d570d/bmr.0024.fig.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/d2928e648c6d/bmr.0024.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/981ad034b0cb/bmr.0024.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/b3079ff40425/bmr.0024.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/a46c05426cbe/bmr.0024.fig.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/3e4a289e3ae3/bmr.0024.fig.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf43/11062504/7a0f6a4d570d/bmr.0024.fig.006.jpg

相似文献

[1]
Accurately Controlled Tumor Temperature with Silica-Coated Gold Nanorods for Optimal Immune Checkpoint Blockade Therapy.

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[2]
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[3]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Smart Biomaterials for Delivery of Drugs and Cells.

Biomater Res. 2025-7-31

[2]
Nanotechnology-Based Strategies for Safe and Effective Immunotherapy.

Molecules. 2024-12-11

本文引用的文献

[1]
Applications and safety of gold nanoparticles as therapeutic devices in clinical trials.

J Pharm Anal. 2023-9

[2]
Imaging-Guided Antibacterial Based on Gold Nanocrystals and Assemblies.

Small Methods. 2024-1

[3]
Activatable Immunoprotease Nanorestimulator for Second Near-Infrared Photothermal Immunotherapy of Cancer.

ACS Nano. 2023-5-9

[4]
Multifunctional Nano-Biomaterials for Cancer Therapy via Inducing Enhanced Immunogenic Cell Death.

Small Methods. 2023-5

[5]
Implantable micro-scale LED device guided photodynamic therapy to potentiate antitumor immunity with mild visible light.

Biomater Res. 2022-10-18

[6]
Clinical translation of gold nanoparticles.

Drug Deliv Transl Res. 2023-2

[7]
Precise control over the silica shell thickness and finding the optimal thickness for the peak heat diffusion property of AuNR@SiO.

J Mater Chem B. 2022-1-19

[8]
Visible-Light-Triggered Prodrug Nanoparticles Combine Chemotherapy and Photodynamic Therapy to Potentiate Checkpoint Blockade Cancer Immunotherapy.

ACS Nano. 2021-7-27

[9]
Activatable polymer nanoagonist for second near-infrared photothermal immunotherapy of cancer.

Nat Commun. 2021-2-2

[10]
Tumor size-dependent abscopal effect of polydopamine-coated all-in-one nanoparticles for immunochemo-photothermal therapy of early- and late-stage metastatic cancer.

Biomaterials. 2021-2

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