Journal article
Protective efficacy of serially up-ranked subdominant CD8+ T cell epitopes against virus challenges.
- Abstract:
- Immunodominance in T cell responses to complex antigens like viruses is still incompletely understood. Some data indicate that the dominant responses to viruses are not necessarily the most protective, while other data imply that dominant responses are the most important. The issue is of considerable importance to the rational design of vaccines, particularly against variable escaping viruses like human immunodeficiency virus type 1 and hepatitis C virus. Here, we showed that sequential inactivation of dominant epitopes up-ranks the remaining subdominant determinants. Importantly, we demonstrated that subdominant epitopes can induce robust responses and protect against whole viruses if they are allowed at least once in the vaccination regimen to locally or temporally dominate T cell induction. Therefore, refocusing T cell immune responses away from highly variable determinants recognized during natural virus infection towards subdominant, but conserved regions is possible and merits evaluation in humans.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 1013.2KB, Terms of use)
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- Publisher copy:
- 10.1371/journal.ppat.1002041
Authors
- Publisher:
- Public Library of Science
- Journal:
- PLoS pathogens More from this journal
- Volume:
- 7
- Issue:
- 5
- Pages:
- e1002041
- Publication date:
- 2011-05-01
- DOI:
- EISSN:
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1553-7374
- ISSN:
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1553-7366
- Language:
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English
- Keywords:
- Pubs id:
-
140613
- UUID:
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uuid:19cc21fe-c57e-4044-9c02-0339a44c44bc
- Local pid:
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pubs:140613
- Source identifiers:
-
140613
- Deposit date:
-
2012-12-19
- ARK identifier:
Terms of use
- Copyright holder:
- Im et al
- Copyright date:
- 2011
- Notes:
- © 2011 Im et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
- Licence:
- CC Attribution (CC BY)
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