BioAcyl Corp |
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| Resource type: Journal Article DOI: 10.1016/j.cell.2022.02.005 ID no. (ISBN etc.): 0092-8674, 1097-4172 BibTeX citation key: Afkhami2022 View all bibliographic details |
Categories: BioAcyl Corp, BioAcyl Corp Subcategories: Covid-19 adenoviral vectors, COVID-19 Vaccines Creators: Afkhami, Ang, Bavananthasivam, D’Agostino, Gameiro, Gillgrass, Jeyanathan, Jordana, Kang, Kazhdan, Koenig, Lichty, Luo, Marzok, Medina, Miller, Mossman, Phelps, Sankar, Singh, Smaill, Stacey, Tang, Wan, Wang, Xing, Ye, Zganiacz, Zhang Collection: Cell |
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| Abstract |
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The emerging SARS-CoV-2 variants of concern (VOC) threaten the effectiveness of current COVID-19 vaccines administered intramuscularly and designed to only target the spike protein. There is a pressing need to develop next-generation vaccine strategies for broader and long-lasting protection. Using adenoviral vectors (Ad) of human and chimpanzee origin, we evaluated Ad-vectored trivalent COVID-19 vaccines expressing Spike-1, Nucleocapsid and RdRp antigens in murine models. We show that single-dose intranasal immunization, particularly with chimpanzee Ad-vectored vaccine, is superior to intramuscular immunization in induction of the tripartite protective immunity consisting of local and systemic antibody responses, mucosal tissue-resident memory T cells and mucosal trained innate immunity. We further show that intranasal immunization provides protection against both the ancestral SARS-CoV-2 and two VOC, B.1.1.7 and B.1.351. Our findings indicate that respiratory mucosal delivery of Ad-vectored multivalent vaccine represents an effective next-generation COVID-19 vaccine strategy to induce all-around mucosal immunity against current and future VOC.
Added by: Dr. Enrique Feoli Last edited by: Dr. Enrique Feoli |
| Notes |
Added by: Dr. Enrique Feoli Last edited by: Dr. Enrique Feoli |