| Literature DB >> 31710460 |
He Zhao1, Jun Xu2, Yan Li1, Xinxian Guan1, Xiao Han2, Yunyun Xu1, Huiting Zhou1, Rui Peng2, Jian Wang1, Zhuang Liu2.
Abstract
Tumor vaccines to induce robust immunity for cancer treatment have attracted tremendous interests in cancer immunotherapy. In this work, a type of cancer vaccine is prepared by using nanoscale coordination polymer (NCP) formed between Mn2+ ions and a nucleotide oligomerization binding domain 1 (Nod1) agonist, meso-2,6-diaminopimelic acid (DAP), as the organic ligand, to encapsulate a model protein antigen, ovalbumin (OVA). The obtained OVA@Mn-DAP nanoparticles could act as an effective tumor vaccine to promote the maturation of dendritic cells (DCs) as well as their antigen cross-presentation via increasing the cellular uptake of antigen and stimulating Nod1 pathway with DAP. Such OVA@Mn-DAP vaccine could migrate into lymph nodes after local injection, as revealed by in vivo magnetic resonance (MR) and fluorescence imaging. Importantly, vaccination with OVA@Mn-DAP could not only offer prophylactic to protect mice from challenged B16-OVA tumors but also result in significant therapeutic effect to inhibit growth of already-established tumors if in combination with anti-programmed cell death protein 1 antibody (α-PD-1) immune checkpoint blockade therapy. Therefore, this work presents an innovative platform to construct effective nanovaccine for tumor immunotherapy.Entities:
Keywords: Nanovaccine; Nod1 agonist; cancer immunotherapy; checkpoint blockade; nanoscale coordination polymer
Year: 2019 PMID: 31710460 DOI: 10.1021/acsnano.9b05974
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881