Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Isinelli, Giorgia | - |
dc.contributor.author | Zeng, Yang Claire | - |
dc.contributor.author | Young, Olivia | - |
dc.contributor.author | Xiong, Qiancheng | - |
dc.contributor.author | Si, Longlong | - |
dc.contributor.author | Ku, Min Wen | - |
dc.contributor.author | Bernier, Sylvie | - |
dc.contributor.author | Dembele, Hawa | - |
dc.contributor.author | Gilboa, Tal | - |
dc.contributor.author | Swank, Zoe | - |
dc.contributor.author | Seok, Su Hyun | - |
dc.contributor.author | Rajwar, Anjali | - |
dc.contributor.author | Jiang, Amanda | - |
dc.contributor.author | Zhai, Yunhao | - |
dc.contributor.author | Hellman, Caleb | - |
dc.contributor.author | Williams, LaTonya | - |
dc.contributor.author | Wintersinger, Chris | - |
dc.contributor.author | Graveline, Amanda | - |
dc.contributor.author | Vernet, Andyna | - |
dc.contributor.author | Sanchez, Melinda | - |
dc.contributor.author | Bardales, Sarai | - |
dc.contributor.author | Tomaras, Georgia | - |
dc.contributor.author | Ryu, Ju Hee | - |
dc.contributor.author | Kwon, Ick Chan | - |
dc.contributor.author | Goyal, Girija | - |
dc.contributor.author | Ingber, Donald | - |
dc.contributor.author | Shih, William | - |
dc.date.accessioned | 2025-07-30T01:30:40Z | - |
dc.date.available | 2025-07-30T01:30:40Z | - |
dc.date.created | 2025-07-30 | - |
dc.date.issued | 2025-05 | - |
dc.identifier.issn | 1525-0016 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/152881 | - |
dc.identifier.uri | https://www.cell.com/molecular-therapy-family/molecular-therapy/issue?pii=S1525-0016(24)X0003-9 | - |
dc.description.abstract | 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 na?ve 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. | - |
dc.language | English | - |
dc.publisher | Nature Publishing Group | - |
dc.title | DNA Origami Vaccine (DoriVac) Nanoparticles Improve Both Humoral and Cellular Immune Responses to Infectious Diseases | - |
dc.type | Conference | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | 28th Annual Meeting of the American Society of Gene & Cell Therapy, v.33, no.5 | - |
dc.citation.title | 28th Annual Meeting of the American Society of Gene & Cell Therapy | - |
dc.citation.volume | 33 | - |
dc.citation.number | 5 | - |
dc.citation.conferencePlace | US | - |
dc.citation.conferencePlace | New Orleans Ernest N. Morial Convention Center, USA | - |
dc.citation.conferenceDate | 2025-05-13 | - |
dc.relation.isPartOf | Molecular Therapy | - |
dc.identifier.wosid | 001505174200006 | - |
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