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dc.contributor.authorIsinelli, Giorgia-
dc.contributor.authorZeng, Yang Claire-
dc.contributor.authorYoung, Olivia-
dc.contributor.authorXiong, Qiancheng-
dc.contributor.authorSi, Longlong-
dc.contributor.authorKu, Min Wen-
dc.contributor.authorBernier, Sylvie-
dc.contributor.authorDembele, Hawa-
dc.contributor.authorGilboa, Tal-
dc.contributor.authorSwank, Zoe-
dc.contributor.authorSeok, Su Hyun-
dc.contributor.authorRajwar, Anjali-
dc.contributor.authorJiang, Amanda-
dc.contributor.authorZhai, Yunhao-
dc.contributor.authorHellman, Caleb-
dc.contributor.authorWilliams, LaTonya-
dc.contributor.authorWintersinger, Chris-
dc.contributor.authorGraveline, Amanda-
dc.contributor.authorVernet, Andyna-
dc.contributor.authorSanchez, Melinda-
dc.contributor.authorBardales, Sarai-
dc.contributor.authorTomaras, Georgia-
dc.contributor.authorRyu, Ju Hee-
dc.contributor.authorKwon, Ick Chan-
dc.contributor.authorGoyal, Girija-
dc.contributor.authorIngber, Donald-
dc.contributor.authorShih, William-
dc.date.accessioned2025-07-30T01:30:40Z-
dc.date.available2025-07-30T01:30:40Z-
dc.date.created2025-07-30-
dc.date.issued2025-05-
dc.identifier.issn1525-0016-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/152881-
dc.identifier.urihttps://www.cell.com/molecular-therapy-family/molecular-therapy/issue?pii=S1525-0016(24)X0003-9-
dc.description.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 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.languageEnglish-
dc.publisherNature Publishing Group-
dc.titleDNA Origami Vaccine (DoriVac) Nanoparticles Improve Both Humoral and Cellular Immune Responses to Infectious Diseases-
dc.typeConference-
dc.description.journalClass1-
dc.identifier.bibliographicCitation28th Annual Meeting of the American Society of Gene & Cell Therapy, v.33, no.5-
dc.citation.title28th Annual Meeting of the American Society of Gene & Cell Therapy-
dc.citation.volume33-
dc.citation.number5-
dc.citation.conferencePlaceUS-
dc.citation.conferencePlaceNew Orleans Ernest N. Morial Convention Center, USA-
dc.citation.conferenceDate2025-05-13-
dc.relation.isPartOfMolecular Therapy-
dc.identifier.wosid001505174200006-
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