Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 645 - 654
Published: Oct. 1, 2024
Language: Английский
Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 645 - 654
Published: Oct. 1, 2024
Language: Английский
Advanced Science, Journal Year: 2025, Volume and Issue: unknown
Published: April 9, 2025
Abstract The incidence of melanoma, the third most common skin cancer, has been on rise in recent years. In addition, it a high mortality rate due to its aggressiveness. Phototherapy, as promising treatment method, can effectively kill tumor cells, but is incapable metastasis. Herein, nanomaterial (TPC@OVA NPs) developed for phototherapy conjunction with immunotherapy against melanoma. TPC, derivative porphyrin, used photosensitizer excellent biosafety and photostability. After assembly ovalbumin (OVA), TPC@OVA NPs vaccine properties formed, which not only ablate primary also induce immunogenic cell death (ICD). DC cells be stimulated mature by exogenous OVA, enhancing immune response tumors further activating T lymphocytes. Combined checkpoint inhibitor aPD‐1, microenvironment reshaped, increased activity are validated. This work highlights potential combining
Language: Английский
Citations
0Advanced Healthcare Materials, Journal Year: 2025, Volume and Issue: unknown
Published: April 24, 2025
Abstract Tumor vaccines have shown great promise for treating various malignancies; however, glioblastoma (GBM), characterized by its immunosuppressive tumor microenvironment, high heterogeneity, and limited accessibility, has achieved only modest clinical benefits. Here, it is reported that GBM cell lysate nanovaccines boosted with TLR9 agonist CpG ODN (GlioVac) via a strategic vaccination regimen achieve complete regression of malignant murine tumors. Subcutaneous administration GlioVac promotes uptake cervical lymph nodes antigen presentation cells, bolstering cross‐presentation infiltration GBM‐specific CD8 + T cells into the tumor. Notably, involving two subcutaneous three intravenous vaccinations not activates systemic anti‐GBM immunity but also further enhances cytotoxic lymphocytes, effectively reshaping “cold” “hot” This approach led to state tumor‐free survival in 5 out 7 mice bearing established GL261 model protection from rechallenge. In an orthotopic hRas‐GBM induced lentiviral plasmid, resulted ≈100% regression. These findings suggest provides personalized therapeutic vaccine strategy glioblastoma.
Language: Английский
Citations
0Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 645 - 654
Published: Oct. 1, 2024
Language: Английский
Citations
0