Nano Today, Journal Year: 2024, Volume and Issue: 58, P. 102465 - 102465
Published: Aug. 27, 2024
Language: Английский
Nano Today, Journal Year: 2024, Volume and Issue: 58, P. 102465 - 102465
Published: Aug. 27, 2024
Language: Английский
Journal of Hematology & Oncology, Journal Year: 2024, Volume and Issue: 17(1)
Published: April 2, 2024
Abstract Cancer immunotherapy and vaccine development have significantly improved the fight against cancers. Despite these advancements, challenges remain, particularly in clinical delivery of immunomodulatory compounds. The tumor microenvironment (TME), comprising macrophages, fibroblasts, immune cells, plays a crucial role response modulation. Nanoparticles, engineered to reshape TME, shown promising results enhancing by facilitating targeted These nanoparticles can suppress fibroblast activation, promote M1 macrophage polarization, aid dendritic cell maturation, encourage T infiltration. Biomimetic further enhance increasing internalization agents cells such as cells. Moreover, exosomes, whether naturally secreted body or bioengineered, been explored regulate TME immune-related affect cancer immunotherapy. Stimuli-responsive nanocarriers, activated pH, redox, light conditions, exhibit potential accelerate co-application with checkpoint inhibitors is an emerging strategy boost anti-tumor immunity. With their ability induce long-term immunity, nanoarchitectures are structures development. This review underscores critical overcoming current driving advancement modification.
Language: Английский
Citations
144Coordination Chemistry Reviews, Journal Year: 2023, Volume and Issue: 501, P. 215560 - 215560
Published: Nov. 27, 2023
Language: Английский
Citations
55Colloids and Surfaces B Biointerfaces, Journal Year: 2024, Volume and Issue: 235, P. 113770 - 113770
Published: Feb. 1, 2024
Language: Английский
Citations
18Advanced Materials, Journal Year: 2023, Volume and Issue: 36(1)
Published: Oct. 21, 2023
Abstract Cancer immunotherapy has become a promising method for cancer treatment, bringing hope to advanced patients. However, immune‐related adverse events caused by also bring heavy burden Semiconducting polymer nanoparticles (SPNs) as an emerging nanomaterial with high biocompatibility, can eliminate tumors and induce tumor immunogenic cell death through different therapeutic modalities, including photothermal therapy, photodynamic sonodynamic therapy. In addition, SPNs work functional nanocarrier synergize variety of immunomodulators amplify anti‐tumor immune responses. this review, SPNs‐based combination is comprehensively summarized according the SPNs’ modalities type loaded immunomodulators. The in‐depth understanding existing will hopefully inspire design more novel nanomaterials potent effects, ultimately promote their clinical translation.
Language: Английский
Citations
42Nano Letters, Journal Year: 2024, Volume and Issue: 24(25), P. 7764 - 7773
Published: June 12, 2024
Inducing immunogenic cell death (ICD) during photothermal therapy (PTT) has the potential to effectively trigger immunotherapy (PTI). However, ICD induced by PTT alone is often limited inefficient PTT, low immunogenicity of tumor cells, and a dysregulated redox microenvironment. Herein, we develop MoSe2 nanosheets with high-percentage metallic 1T phase rich exposed active Mo centers through defect engineering as an effective nanoagent for PTI. The in endows them strong performance, abundant endow high activity glutathione (GSH) depletion. MoSe2-mediated high-performance synergizing efficient GSH depletion facilitates release tumor-associated antigens induce robust ICD, thus significantly enhancing checkpoint blockade activating systemic immune response mouse models colorectal cancer triple-negative metastatic breast cancer.
Language: Английский
Citations
14Advanced Functional Materials, Journal Year: 2024, Volume and Issue: unknown
Published: July 2, 2024
Abstract Recent advances are achieved in the design and development of efficient organic photosensitizers (PSs), especially with fluorescence imaging navigation second near‐infrared (NIR‐II, 1000–1700 nm) region. However, there simply a handful NIR‐II emissive PSs oxygen‐independent capability due to scarcity high‐performance NIR‐responsive materials targeted delivery. Herein, NIR‐II‐emissive nanomedicine biomimetic engineering for multiple phototherapies pancreatic tumors is reported. An A‐D‐A‐type conjugated small‐molecule TPC designed used prepare water‐dispersive nanoparticles, which demonstrated high efficiency type I II photodynamic performances, good photothermal conversion 57%, bright emission quantum yield 9.8% under 808 nm light irradiation. With cancer cell membrane camouflage, high‐resolution bioimaging whole‐body blood vessels tumors. Antitumor experiments tumor elimination biosafety This work versatile enhanced tumor‐targeting superior phototheranostics, providing feasible idea evolution theranostics.
Language: Английский
Citations
11International Journal of Nanomedicine, Journal Year: 2024, Volume and Issue: Volume 19, P. 1249 - 1272
Published: Feb. 1, 2024
Background: The anti-Programmed Death-Ligand 1 (termed aPD-L1) immune checkpoint blockade therapy has emerged as a promising treatment approach for various advanced solid tumors. However, the effect of aPD-L1 inhibitors limited by tumor microenvironment makes most patients exhibit immunotherapy resistance. Methods: We conjugated Sialyl Lewis X with polyethylene glycol-coated ultrasmall superparamagnetic iron oxide (USPIO-PEG) to form UPS nanoparticles (USPIO-PEG-SLe x , termed UPS). physicochemical properties were tested and characterized. Transmission electron microscopy ICP-OES used observe cellular uptake targeting ability UPS. Flow cytometry, mitochondrial membrane potential staining, live-dead staining scratch assay verify in vitro photothermal UPS, stimulation on immune-related pathways at gene level was analyzed sequencing. Biological safety analysis pharmacokinetic performed. Finally, amplification UPS-mediated aPD-L1-mediated corresponding mechanism studied. Results: In experiments showed that had strong able stimulate 5 pathways. vivo, when PTT assisted treatment, it exhibited significant increase CD4 + T cell infiltration 14.46-fold CD8 14.79-fold, along elevated secretion necrosis factor-alpha interferon-gamma, comparing alone aPD-L1. This achieved inhibition both primary tumors distant compared aPD-L1, demonstrating difference. Conclusion: nanotheranostic agent been introduced into immunotherapy, which effectively broadened its application biomedicine. therapeutic enhancing efficacy therapy, can be instructive address challenges associated resistance, thereby offering clinical translation. Keywords: blockade, agent,
Language: Английский
Citations
7International Journal of Pharmaceutics, Journal Year: 2024, Volume and Issue: 656, P. 124045 - 124045
Published: March 30, 2024
Language: Английский
Citations
7Journal of Controlled Release, Journal Year: 2024, Volume and Issue: 367, P. 354 - 365
Published: Feb. 1, 2024
Language: Английский
Citations
6Biomaterials, Journal Year: 2023, Volume and Issue: 305, P. 122434 - 122434
Published: Dec. 17, 2023
Language: Английский
Citations
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