Biomimetic Nano-Immunoactivator via Ionic Metabolic Modulation for Strengthened NIR-II Photothermal Immunotherapy.
Xiaodan WeiHonglin HuangJunhan GuoNingxi LiQingzhi LiTian ZhaoGeng YangLulu CaiHong YangChunhui WuYiyao LiuPublished in: Small (Weinheim an der Bergstrasse, Germany) (2023)
Reprogramming the immunologically "cold" environment of solid tumors is currently becoming the mainstream strategy to elicit powerful and systemic anticancer immunity. Here, a facile and biomimetic nano-immunnoactivator (CuS/Z@M 4T1 ) is detailed by engineering a Zn 2+ -bonded zeolitic imidazolate framework-8 (ZIF-8) with CuS nanodots (NDs) and cancer cell membrane for amplified near-infrared-II (NIR-II) photothermal immunotherapy via Zn 2+ metabolic modulation. Taking advantage of the NIR-II photothermal effect of CuS NDs and the acidic responsiveness of ZIF-8, CuS/Z@M 4T1 rapidly causes intracellular Zn 2+ pool overload and disturbs the metabolic flux of 4T1 cells, which effectively hamper the production of heat shock proteins and relieve the resistance of photothermal therapy (PTT). Thus, amplified immunogenic cell death is evoked and initiates the immune cascade both in vivo and in vitro as demonstrated by dendritic cells maturation and T-cell infiltration. Further combination with antiprogrammed death 1 (aPD-1) achieves escalated antitumor efficacy which eliminates the primary, distant tumor and avidly inhibits lung metastasis due to cooperation of enhanced photothermal stimulation and empowerment of cytotoxic T lymphocytes by aPD-1. Collectively, this work provides the first report of using the intrinsic modulation property of meta-organometallic ZIF-8 for enhanced cancer photoimmunotherapy together with aPD-1, thereby inspiring a novel combined paradigm of ion-rich nanomaterials for cancer treatment.
Keyphrases
- photodynamic therapy
- drug release
- dendritic cells
- cancer therapy
- heat shock
- drug delivery
- papillary thyroid
- cell death
- fluorescence imaging
- heavy metals
- squamous cell
- immune response
- ionic liquid
- risk assessment
- squamous cell carcinoma
- oxidative stress
- lymph node
- quantum dots
- gold nanoparticles
- cell proliferation
- heat shock protein
- young adults
- signaling pathway
- reduced graphene oxide