A genetically engineered, stem-cell-derived cellular vaccine.
dc.contributor.author | Cooper, Amanda | |
dc.contributor.author | Sidaway, Adam | |
dc.contributor.author | Chandrashekar, Abishek | |
dc.contributor.author | Latta, Elizabeth | |
dc.contributor.author | Chakraborty, Krishnendu | |
dc.contributor.author | Yu, Jingyou | |
dc.contributor.author | McMahan, Katherine | |
dc.contributor.author | Giffin, Victoria | |
dc.contributor.author | Manickam, Cordelia | |
dc.contributor.author | Kroll, Kyle | |
dc.contributor.author | Mosher, Matthew | |
dc.contributor.author | Reeves, R Keith | |
dc.contributor.author | Gam, Rihab | |
dc.contributor.author | Arthofer, Elisa | |
dc.contributor.author | Choudhry, Modassir | |
dc.contributor.author | Henley, Tom | |
dc.contributor.author | Barouch, Dan H | |
dc.date.accessioned | 2023-02-01T17:20:56Z | |
dc.date.available | 2023-02-01T17:20:56Z | |
dc.date.issued | 2022-12 | |
dc.date.updated | 2023-02-01T17:20:25Z | |
dc.description.abstract | Despite rapid clinical translation of COVID-19 vaccines in response to the global pandemic, an opportunity remains for vaccine technology innovation to address current limitations and meet challenges of inevitable future pandemics. We describe a universal vaccine cell (UVC) genetically engineered to mimic natural physiological immunity induced upon viral infection of host cells. Cells engineered to express the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike as a representative viral antigen induce robust neutralizing antibodies in immunized non-human primates. Similar titers generated in this established non-human primate (NHP) model have translated into protective human neutralizing antibody levels in SARS-CoV-2-vaccinated individuals. Animals vaccinated with ancestral spike antigens and subsequently challenged with SARS-CoV-2 Delta variant in a heterologous challenge have an approximately 3 log decrease in viral subgenomic RNA in the lungs. This cellular vaccine is designed as a scalable cell line with a modular poly-antigenic payload, allowing for rapid, large-scale clinical manufacturing and use in an evolving viral variant environment. | |
dc.identifier | S2666-3791(22)00407-4 | |
dc.identifier.issn | 2666-3791 | |
dc.identifier.issn | 2666-3791 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Elsevier BV | |
dc.relation.ispartof | Cell reports. Medicine | |
dc.relation.isversionof | 10.1016/j.xcrm.2022.100843 | |
dc.subject | Animals | |
dc.subject | Humans | |
dc.subject | Viral Vaccines | |
dc.subject | Antibodies, Viral | |
dc.subject | Antibodies, Neutralizing | |
dc.subject | COVID-19 | |
dc.subject | SARS-CoV-2 | |
dc.subject | COVID-19 Vaccines | |
dc.title | A genetically engineered, stem-cell-derived cellular vaccine. | |
dc.type | Journal article | |
duke.contributor.orcid | Reeves, R Keith|0000-0003-3157-2557 | |
pubs.begin-page | 100843 | |
pubs.issue | 12 | |
pubs.organisational-group | Duke | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Pathology | |
pubs.organisational-group | Surgery | |
pubs.organisational-group | Surgery, Surgical Sciences | |
pubs.publication-status | Published | |
pubs.volume | 3 |
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