Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts02139, United States.
Nanotechnology Characterization Laboratory, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland21702, United States.
ACS Nano. 2022 Dec 27;16(12):20340-20352. doi: 10.1021/acsnano.2c06275. Epub 2022 Dec 2.
Three-dimensional wireframe DNA origami have programmable structural and sequence features that render them potentially suitable for prophylactic and therapeutic applications. However, their innate immunological properties, which stem from parameters including geometric shape and cytosine-phosphate-guanine dinucleotide (CpG) content, remain largely unknown. Here, we investigate the immunostimulatory properties of 3D wireframe DNA origami on the TLR9 pathway using both reporter cell lines and primary immune cells. Our results suggest that bare 3D polyhedral wireframe DNA origami induce minimal TLR9 activation despite the presence of numerous internal CpG dinucleotides. However, when displaying multivalent CpG-containing ssDNA oligos, wireframe DNA origami induce robust TLR9 pathway activation, along with enhancement of downstream immune response as evidenced by increases in Type I and Type III interferon (IFN) production in peripheral blood mononuclear cells. Further, we find that CpG copy number and spatial organization each contribute to the magnitude of TLR9 signaling and that NANP-attached CpGs do not require phosphorothioate stabilization to elicit signaling. These results suggest key design parameters for wireframe DNA origami that can be programmed to modulate immune pathway activation controllably for prophylactic and therapeutic applications.
三维线框 DNA 折纸具有可编程的结构和序列特征,使其具有潜在的预防和治疗应用价值。然而,它们的固有免疫特性,源于包括几何形状和胞嘧啶-磷酸-鸟嘌呤二核苷酸 (CpG) 含量在内的参数,在很大程度上仍不清楚。在这里,我们使用报告细胞系和原代免疫细胞研究了 3D 线框 DNA 折纸在 TLR9 途径上的免疫刺激特性。我们的结果表明,尽管存在许多内部 CpG 二核苷酸,但裸露的 3D 多面体线框 DNA 折纸仅诱导最小的 TLR9 激活。然而,当展示多价含 CpG 的 ssDNA 寡核苷酸时,线框 DNA 折纸会诱导强烈的 TLR9 途径激活,并增强下游免疫反应,这表现在外周血单核细胞中 I 型和 III 型干扰素 (IFN) 的产生增加。此外,我们发现 CpG 拷贝数和空间组织都对线粒体 9 信号的幅度有贡献,并且 NANP 附着的 CpG 不需要磷硫代稳定化来引发信号。这些结果表明了线框 DNA 折纸的关键设计参数,可以编程以可控的方式调节免疫途径激活,用于预防和治疗应用。