Yang C. Zeng, Olivia J. Young, L. Si, Min Wen Ku, Giorgia Isinelli, Anjali Rajwar, Amanda Jiang, Chris M. Wintersinger, A. Graveline, A. Vernet, Melinda Sanchez, Ju Hee Ryu, Ick Chan Kwon, G. Goyal, Donald E. Ingber, William M. Shih
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引用次数: 0
摘要
目前的 SARS-CoV-2 疫苗已证明能强有力地诱导中和抗体和 CD4+ T 细胞活化,但 CD8+ 反应不稳定,免疫持续时间和对变异体的保护有限。在此,我们将 DNA 折纸疫苗平台 DoriVac 改用于针对传染性病毒,即 SARS-CoV-2、HIV 和埃博拉病毒。DNA 折纸纳米粒子与传染病特异性 HR2 肽(作为高度保守的抗原)和 CpG 佐剂以精确的纳米级间距共轭,可诱导天真小鼠体内的中和抗体、Th1 CD4+ T 细胞和 CD8+ T 细胞,与药丸对照组相比有显著改善。使用淋巴结芯片系统进行的临床前研究证实,DoriVac 与抗原肽或蛋白质结合后,可诱导人体细胞产生良好的细胞免疫反应。这些结果表明,DoriVac 具有作为多功能模块化疫苗平台的潜力,能够诱导体液免疫和细胞免疫。该平台的可编程性强调了它在应对未来流行病方面的潜在作用。
DNA origami vaccine (DoriVac) nanoparticles improve both humoral and cellular immune responses to infectious diseases
Current SARS-CoV-2 vaccines have demonstrated robust induction of neutralizing antibodies and CD4+ T cell activation, however CD8+ responses are variable, and the duration of immunity and protection against variants are limited. Here we repurposed our DNA origami vaccine platform, DoriVac, for targeting infectious viruses, namely SARS-CoV-2, HIV, and Ebola. The DNA origami nanoparticle, conjugated with infectious-disease-specific HR2 peptides, which act as highly conserved antigens, and CpG adjuvant at precise nanoscale spacing, induced neutralizing antibodies, Th1 CD4+ T cells, and CD8+ T cells in naïve mice, with significant improvement over a bolus control. Pre-clinical studies using lymph-node-on-a-chip systems validated that DoriVac, when conjugated with antigenic peptides or proteins, induced promising cellular immune responses in human cells. These results suggest that DoriVac holds potential as a versatile, modular vaccine platform, capable of inducing both humoral and cellular immunities. The programmability of this platform underscores its potential utility in addressing future pandemics.