Department of Cancer Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, MA, USA.
Nat Nanotechnol. 2024 Jul;19(7):1055-1065. doi: 10.1038/s41565-024-01615-3. Epub 2024 Mar 15.
Multivalent presentation of ligands often enhances receptor activation and downstream signalling. DNA origami offers a precise nanoscale spacing of ligands, a potentially useful feature for therapeutic nanoparticles. Here we use a square-block DNA origami platform to explore the importance of the spacing of CpG oligonucleotides. CpG engages Toll-like receptors and therefore acts to activate dendritic cells. Through in vitro cell culture studies and in vivo tumour treatment models, we demonstrate that square blocks induce Th1 immune polarization when CpG is spaced at 3.5 nm. We observe that this DNA origami vaccine enhances DC activation, antigen cross-presentation, CD8 T-cell activation, Th1-polarized CD4 activation and natural-killer-cell activation. The vaccine also effectively synergizes with anti-PD-L1 for improved cancer immunotherapy in melanoma and lymphoma models and induces long-term T-cell memory. Our results suggest that DNA origami may serve as a platform for controlling adjuvant spacing and co-delivering antigens in vaccines.
配体的多价呈现通常会增强受体激活和下游信号转导。DNA 折纸术提供了配体的精确纳米级间距,这是治疗性纳米颗粒的一个潜在有用特征。在这里,我们使用正方形 DNA 折纸平台来探索 CpG 寡核苷酸间距的重要性。CpG 与 Toll 样受体结合,因此能够激活树突状细胞。通过体外细胞培养研究和体内肿瘤治疗模型,我们证明当 CpG 间隔 3.5nm 时,正方形块会诱导 Th1 免疫极化。我们观察到这种 DNA 折纸疫苗增强了 DC 的激活、抗原交叉呈递、CD8 T 细胞的激活、Th1 极化的 CD4 激活和自然杀伤细胞的激活。该疫苗还与抗 PD-L1 有效协同,在黑色素瘤和淋巴瘤模型中改善癌症免疫治疗,并诱导长期 T 细胞记忆。我们的结果表明,DNA 折纸术可用作控制佐剂间距和在疫苗中共同递呈抗原的平台。