Journal article
Potent CD8+ T-cell immunogenicity in humans of a novel heterosubtypic influenza A vaccine, MVA-NP+M1.
- Abstract:
-
Background.
Influenza A viruses cause occasional pandemics and frequent epidemics. Licensed influenza vaccines that induce high antibody titers to the highly polymorphic viral surface antigen hemagglutinin must be re-formulated and readministered annually. A vaccine providing protective immunity to the highly conserved internal antigens could provide longer-lasting protection against multiple influenza subtypes.Methods.
We prepared a Modified Vaccinia virus Ankara (MVA) vector encoding nucleoprotein and matrix protein 1 (MVA−NP+M1) and conducted a phase I clinical trial in healthy adults.Results.
The vaccine was generally safe and well tolerated, with significantly fewer local side effects after intramuscular rather than intradermal administration. Systemic side effects increased at the higher dose in both frequency and severity, with 5 out of 8 volunteers experiencing severe nausea/vomiting, malaise, or rigors. Ex vivo T-cell responses to NP and M1 measured by IFN-γ ELISPOT assay were significantly increased after vaccination (prevaccination median of 123 spot-forming units/million peripheral blood mononuclear cells, postvaccination peak response median 339, 443, and 1443 in low-dose intradermal, low-dose intramuscular, and high-dose intramuscular groups, respectively), and the majority of the antigen-specific T cells were CD8+.Conclusions.
We conclude that the vaccine was both safe and remarkably immunogenic, leading to frequencies of responding T cells that appear to be much higher than those induced by any other influenza vaccination approach. Further studies will be required to find the optimum dose and to assess whether the increased T-cell response to conserved influenza proteins results in protection from influenza disease.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Access Document
- Files:
-
-
(Preview, Version of record, pdf, 187.7KB, Terms of use)
-
- Publisher copy:
- 10.1093/cid/ciq015
Authors
- Publisher:
- Oxford University Press
- Journal:
- Clinical infectious diseases : an official publication of the Infectious Diseases Society of America More from this journal
- Volume:
- 52
- Issue:
- 1
- Pages:
- 1-7
- Publication date:
- 2011-01-01
- DOI:
- EISSN:
-
1537-6591
- ISSN:
-
1058-4838
- Language:
-
English
- Keywords:
-
- Pubs id:
-
107021
- UUID:
-
uuid:6ce39c29-b163-4a68-a071-ec42f5c57ab7
- Local pid:
-
pubs:107021
- Source identifiers:
-
107021
- Deposit date:
-
2012-12-19
- ARK identifier:
Terms of use
- Copyright holder:
- Berthoud et al
- Copyright date:
- 2011
- Notes:
- Copyright Berthoud et al. 2013. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
If you are the owner of this record, you can report an update to it here: Report update to this record