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MCMV-based vaccine vectors expressing full-length viral proteins provide long-term humoral immune protection upon a single-shot vaccination

Abstract:
Abstract Global pandemics caused by influenza or coronaviruses cause severe disruptions to public health and lead to high morbidity and mortality. There remains a medical need for vaccines against these pathogens. CMV (cytomegalovirus) is a β-herpesvirus that induces uniquely robust immune responses in which remarkably large populations of antigen-specific CD8 T cells are maintained for a lifetime. Hence, CMV has been proposed and investigated as a novel vaccine vector for expressing antigenic peptides or proteins to elicit protective cellular immune responses against numerous pathogens. We generated two recombinant murine CMV (MCMV) vaccine vectors expressing hemagglutinin (HA) of influenza A virus (MCMV ) or the spike protein of severe acute respiratory syndrome coronavirus 2 (MCMV ). A single injection of MCMVs expressing either viral protein induced potent neutralizing antibody responses, which strengthened over time. Importantly, MCMV -vaccinated mice were protected from illness following challenge with the influenza virus, and we excluded that this protection was due to the effects of memory T cells. Conclusively, we show here that MCMV vectors induce not only long-term cellular immunity but also humoral responses that provide long-term immune protection against clinically relevant respiratory pathogens
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41423-021-00814-5

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Role:
Author
ORCID:
0009-0005-6703-1228
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Role:
Author
ORCID:
0000-0001-9863-8528
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Role:
Author
ORCID:
0000-0002-1372-4257
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Role:
Author
ORCID:
0000-0001-6477-1785


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Funder identifier:
10.13039/501100009318
Grant:
PIE-0008
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Funder identifier:
10.13039/501100004543


Publisher:
Springer Nature [academic journals on nature.com]
Journal:
Cellular & Molecular Immunology More from this journal
Volume:
19
Issue:
2
Pages:
234-244
Publication date:
2022-01-06
DOI:
EISSN:
2042-0226
ISSN:
1672-7681


Language:
English
Keywords:
Pubs id:
1231470
Local pid:
pubs:1231470
Source identifiers:
W4225411516
Deposit date:
2026-04-09
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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