A single-dose of intranasal vaccination with a live-attenuated SARS-CoV-2 vaccine candidate promotes protective mucosal and systemic immunity
An attenuated SARS-CoV-2 virus with modified viral transcriptional regulatory sequences and deletion of open-reading frames 3, 6, 7 and 8 (∆3678) was previously reported to protect hamsters from SARS-CoV-2 infection and transmission. Here we report that a single-dose intranasal vaccination of ∆3678 protects K18-hACE2 mice from wild-type or variant SARS-CoV-2 challenge. Compared with wild-type virus infection, the ∆3678 vaccination induces equivalent or higher levels of lung and systemic T cell, B cell, IgA, and IgG responses. The results suggest ∆3678 as an attractive mucosal vaccine candidate to boost pulmonary immunity against SARS-CoV-2.
Errataetall: |
UpdateIn: NPJ Vaccines. 2023 Oct 20;8(1):160. - PMID 37863935 |
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Medienart: |
E-Artikel |
Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - year:2023 |
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Enthalten in: |
bioRxiv : the preprint server for biology - (2023) vom: 18. Apr. |
Sprache: |
Englisch |
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Beteiligte Personen: |
Adam, Awadalkareem [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Revised 27.10.2023 published: Electronic UpdateIn: NPJ Vaccines. 2023 Oct 20;8(1):160. - PMID 37863935 Citation Status PubMed-not-MEDLINE |
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doi: |
10.1101/2023.04.17.537235 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM356350185 |
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520 | |a An attenuated SARS-CoV-2 virus with modified viral transcriptional regulatory sequences and deletion of open-reading frames 3, 6, 7 and 8 (∆3678) was previously reported to protect hamsters from SARS-CoV-2 infection and transmission. Here we report that a single-dose intranasal vaccination of ∆3678 protects K18-hACE2 mice from wild-type or variant SARS-CoV-2 challenge. Compared with wild-type virus infection, the ∆3678 vaccination induces equivalent or higher levels of lung and systemic T cell, B cell, IgA, and IgG responses. The results suggest ∆3678 as an attractive mucosal vaccine candidate to boost pulmonary immunity against SARS-CoV-2 | ||
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700 | 1 | |a Xie, Xuping |e verfasserin |4 aut | |
700 | 1 | |a Wang, Tian |e verfasserin |4 aut | |
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