Mesoporous silica nanoparticles loaded Au nanodots: a self-amplifying immunotherapeutic depot for photothermal immunotherapy

IntroductionPhotothermal therapy (PTT) has emerged as a highly promising approach for cancer treatment due to its advantages of localized treatment, controllable irradiation, and non-invasive nature. This study presents a multifunctional platform for tumor PTT based on Au nanoparticles-decorated mes...

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Main Authors: Chuan Wang, Dongmei Wang, Liang Huang, Qi An
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-06-01
Series:Frontiers in Immunology
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Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2025.1616539/full
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author Chuan Wang
Dongmei Wang
Liang Huang
Qi An
author_facet Chuan Wang
Dongmei Wang
Liang Huang
Qi An
author_sort Chuan Wang
collection DOAJ
description IntroductionPhotothermal therapy (PTT) has emerged as a highly promising approach for cancer treatment due to its advantages of localized treatment, controllable irradiation, and non-invasive nature. This study presents a multifunctional platform for tumor PTT based on Au nanoparticles-decorated mesoporous silica nanoparticles (MSN@Au), aiming to synergize photothermal ablation with immune modulation.MethodsMSN@Au nanoparticles were engineered as the PTT agent. Photothermal efficiency was evaluated under 808 nm near-infrared (NIR) laser irradiation. Anti-tumor efficacy was systematically assessed both in vitro (tumor cell cultures) and in vivo (tumor-bearing animal models). Immune responses were analyzed by examining immunogenic cell death (ICD) induction, dendritic cell maturation, and cytotoxic T cell activation/infiltration within the tumor microenvironment (TME).ResultsMSN@Au demonstrated exceptional photothermal conversion efficiency under NIR irradiation, leading to significant tumor cell inhibition in both in vitro and in vivo. Mild PTT mediated by MSN@Au not only caused direct tumor cell damage but also triggered ICD. This promoted dendritic cell maturation and enhanced activation/infiltration of cytotoxic T cells within the TME, thereby amplifying anti-tumor immunity.DiscussionThis study underscores that the strategic design of MSN@Au as a PTT agent successfully induces ICD while modulating the immunosuppressive TME, significantly amplifying therapeutic efficacy. The integration of efficient photothermal ablation with immune activation opens new avenues for developing next-generation nanoplatforms that synergize PTT with immune modulation, offering a promising strategy for treating solid tumors.
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spelling doaj-art-831a40a9f71f4922928f54d5c3f8bcf02025-08-20T02:35:50ZengFrontiers Media S.A.Frontiers in Immunology1664-32242025-06-011610.3389/fimmu.2025.16165391616539Mesoporous silica nanoparticles loaded Au nanodots: a self-amplifying immunotherapeutic depot for photothermal immunotherapyChuan WangDongmei WangLiang HuangQi AnIntroductionPhotothermal therapy (PTT) has emerged as a highly promising approach for cancer treatment due to its advantages of localized treatment, controllable irradiation, and non-invasive nature. This study presents a multifunctional platform for tumor PTT based on Au nanoparticles-decorated mesoporous silica nanoparticles (MSN@Au), aiming to synergize photothermal ablation with immune modulation.MethodsMSN@Au nanoparticles were engineered as the PTT agent. Photothermal efficiency was evaluated under 808 nm near-infrared (NIR) laser irradiation. Anti-tumor efficacy was systematically assessed both in vitro (tumor cell cultures) and in vivo (tumor-bearing animal models). Immune responses were analyzed by examining immunogenic cell death (ICD) induction, dendritic cell maturation, and cytotoxic T cell activation/infiltration within the tumor microenvironment (TME).ResultsMSN@Au demonstrated exceptional photothermal conversion efficiency under NIR irradiation, leading to significant tumor cell inhibition in both in vitro and in vivo. Mild PTT mediated by MSN@Au not only caused direct tumor cell damage but also triggered ICD. This promoted dendritic cell maturation and enhanced activation/infiltration of cytotoxic T cells within the TME, thereby amplifying anti-tumor immunity.DiscussionThis study underscores that the strategic design of MSN@Au as a PTT agent successfully induces ICD while modulating the immunosuppressive TME, significantly amplifying therapeutic efficacy. The integration of efficient photothermal ablation with immune activation opens new avenues for developing next-generation nanoplatforms that synergize PTT with immune modulation, offering a promising strategy for treating solid tumors.https://www.frontiersin.org/articles/10.3389/fimmu.2025.1616539/fullAu nanodotsmesoporous silica nanoparticlesphotothermal immunotherapyimmunogenic cell deathT-cell infiltration
spellingShingle Chuan Wang
Dongmei Wang
Liang Huang
Qi An
Mesoporous silica nanoparticles loaded Au nanodots: a self-amplifying immunotherapeutic depot for photothermal immunotherapy
Frontiers in Immunology
Au nanodots
mesoporous silica nanoparticles
photothermal immunotherapy
immunogenic cell death
T-cell infiltration
title Mesoporous silica nanoparticles loaded Au nanodots: a self-amplifying immunotherapeutic depot for photothermal immunotherapy
title_full Mesoporous silica nanoparticles loaded Au nanodots: a self-amplifying immunotherapeutic depot for photothermal immunotherapy
title_fullStr Mesoporous silica nanoparticles loaded Au nanodots: a self-amplifying immunotherapeutic depot for photothermal immunotherapy
title_full_unstemmed Mesoporous silica nanoparticles loaded Au nanodots: a self-amplifying immunotherapeutic depot for photothermal immunotherapy
title_short Mesoporous silica nanoparticles loaded Au nanodots: a self-amplifying immunotherapeutic depot for photothermal immunotherapy
title_sort mesoporous silica nanoparticles loaded au nanodots a self amplifying immunotherapeutic depot for photothermal immunotherapy
topic Au nanodots
mesoporous silica nanoparticles
photothermal immunotherapy
immunogenic cell death
T-cell infiltration
url https://www.frontiersin.org/articles/10.3389/fimmu.2025.1616539/full
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AT lianghuang mesoporoussilicananoparticlesloadedaunanodotsaselfamplifyingimmunotherapeuticdepotforphotothermalimmunotherapy
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