Biomimetic Dual-Target Theranostic Nanovaccine Enables Magnetic Resonance Imaging and Chemo/Chemodynamic/Immune Therapy of Glioma.
Tianyu HuangYunqi GuoZhiqiang WangJie MaXiangyang ShiXiangyang ShiShaojun PengPublished in: ACS applied materials & interfaces (2024)
Development of theranostic nanomedicines to tackle glioma remains to be challenging. Here, we present an advanced blood-brain barrier (BBB)-crossing nanovaccine based on cancer cell membrane-camouflaged poly( N -vinylcaprolactam) (PVCL) nanogels (NGs) incorporated with MnO 2 and doxorubicin (DOX). We show that the disulfide bond-cross-linked redox-responsive PVCL NGs can be functionalized with dermorphin and imiquimod R837 through cell membrane functionalization. The formed functionalized PVCL NGs having a size of 220 nm are stable, can deplete glutathione, and responsively release both Mn 2+ and DOX under the simulated tumor microenvironment to exert the chemo/chemodynamic therapy mediated by DOX and Mn 2+ , respectively. The combined therapy induces tumor immunogenic cell death to maturate dendritic cells (DCs) and activate tumor-killing T cells. Further, the nanovaccine composed of cancer cell membranes as tumor antigens, R837 as an adjuvant with abilities of DC maturation and macrophages M1 repolarization, and MnO 2 with Mn 2+ -mediated stimulator of interferon gene activation of tumor cells can effectively act on both targets of tumor cells and immune cells. With the dermorphin-mediated BBB crossing, cell membrane-mediated homologous tumor targeting, and Mn 2+ -facilitated magnetic resonance (MR) imaging property, the designed NG-based theranostic nanovaccine enables MR imaging and combination chemo-, chemodynamic-, and imnune therapy of orthotopic glioma with a significantly decreased recurrence rate.
Keyphrases
- blood brain barrier
- photodynamic therapy
- dendritic cells
- cancer therapy
- magnetic resonance imaging
- magnetic resonance
- cell death
- contrast enhanced
- room temperature
- immune response
- early stage
- computed tomography
- squamous cell carcinoma
- gene expression
- combination therapy
- quantum dots
- metal organic framework
- mesenchymal stem cells
- cell proliferation
- copy number
- young adults
- transition metal
- signaling pathway
- radiation therapy
- papillary thyroid
- transcription factor
- mass spectrometry
- brain injury
- smoking cessation
- cell therapy
- genome wide identification