Endoplasmic Reticulum-Targeting Self-Assembly Nanosheets Promote Autophagy and Regulate Immunosuppressive Tumor Microenvironment for Efficient Photodynamic Immunotherapy.
Pei-Ying HuangShi-Yu LiangYun XiangMing-Rui LiMei-Rong WangLi-Han LiuPublished in: Small (Weinheim an der Bergstrasse, Germany) (2024)
The poor efficiency and low immunogenicity of photodynamic therapy (PDT), and the immunosuppressive tumor microenvironment (ITM) lead to tumor recurrence and metastasis. In this work, TCPP-T ER -Zn@RSV nanosheets (TZR NSs) that co-assembled from the endoplasmic reticulum (ER)-targeting photosensitizer TCPP-T ER -Zn nanosheets (TZ NSs for short) and the autophagy promoting and indoleamine-(2, 3)-dioxygenase (IDO) inhibitor-like resveratrol (RSV) are fabricated to enhance antitumor PDT. TZR NSs exhibit improved therapeutic efficiency and amplified immunogenic cancer cell death (ICD) by ER targeting PDT and ER autophagy promotion. TZR NSs reversed the ITM with an increase of CD8+ T cells and reduce of immunosuppressive Foxp3 regulatory T cells, which effectively burst antitumor immunity thus clearing residual tumor cells. The ER-targeting TZR NSs developed in this paper presents a simple but valuable reference for high-efficiency tumor photodynamic immunotherapy.
Keyphrases
- endoplasmic reticulum
- photodynamic therapy
- cell death
- regulatory t cells
- cancer therapy
- high efficiency
- endoplasmic reticulum stress
- fluorescence imaging
- oxidative stress
- signaling pathway
- quantum dots
- reduced graphene oxide
- dendritic cells
- estrogen receptor
- breast cancer cells
- drug delivery
- squamous cell carcinoma
- metal organic framework
- cell cycle arrest
- high frequency
- respiratory syncytial virus
- papillary thyroid
- squamous cell
- lymph node metastasis