Orchestrated Cytosolic Delivery of Antigen and Adjuvant by Manganese Ion-Coordinated Nanovaccine for Enhanced Cancer Immunotherapy.
Zhen-Lin GaoWei XuSui-Juan ZhengQi-Jia DuanRong LiuJin-Zhi DuPublished in: Nano letters (2023)
Cancer vaccines have received tremendous attention in cancer immunotherapy due to their capability to induce a tumor-specific immune response. However, their effectiveness is compromised by the insufficient spatiotemporal delivery of antigens and adjuvants in the subcellular level to induce a robust CD8 + T cell response. Herein, a cancer nanovaccine G5-pBA/OVA@Mn is prepared through multiple interactions of manganese ions (Mn 2+ ), benzoic acid (BA)-modified fifth generation polyamidoamine (G5-PAMAM) dendrimer, and the model protein antigen ovalbumin (OVA). In the nanovaccine, Mn 2+ not only exerts a structural function to assist OVA loading as well as its endosomal escape, but works as an adjuvant of stimulator of interferon genes (STING) pathway. These collaboratively facilitate the orchestrated codelivery of OVA antigen and Mn 2+ into cell cytoplasm. Vaccination with G5-pBA/OVA@Mn not only shows a prophylactic effect, but also significantly inhibits growth against B16-OVA tumors, indicating its great potential for cancer immunotherapy.
Keyphrases
- room temperature
- papillary thyroid
- immune response
- transition metal
- metal organic framework
- early stage
- dendritic cells
- squamous cell
- randomized controlled trial
- systematic review
- squamous cell carcinoma
- genome wide
- single cell
- lymph node metastasis
- stem cells
- toll like receptor
- risk assessment
- mesenchymal stem cells
- amino acid
- protein protein