Author:
Zeng Yang C.,Young Olivia J.,Si Longlong,Ku Min Wen,Isinelli Giorgia,Rajwar Anjali,Jiang Amanda,Wintersinger Chris M.,Graveline Amanda R.,Vernet Andyna,Sanchez Melinda,Ryu Ju Hee,Kwon Ick Chan,Goyal Girija,Ingber Donald E.,Shih William M.
Abstract
AbstractCurrent 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.
Publisher
Cold Spring Harbor Laboratory
Cited by
3 articles.
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