Enumeration of Haemagglutinin-specific CD8⁺ T Cells after Influenza Vaccination Using MHC Class I Peptide Tetramers
With emergence of MHC class I tetramers loaded with CD8⁺ T-cell viral epitopes, it is possible to study virus-specific CD8 cells in humans during infection and after vaccination. MHC class I tetramers was used to detect the frequency of haemagglutinin (HA)-specific T cells in 26 healthy influenza-va...
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Published in: | Scandinavian journal of immunology Vol. 67; no. 1; pp. 86 - 94 |
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Main Authors: | , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Oxford, UK
Oxford, UK : Blackwell Publishing Ltd
2008
Blackwell Publishing Ltd |
Subjects: | |
Online Access: | Get full text |
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Summary: | With emergence of MHC class I tetramers loaded with CD8⁺ T-cell viral epitopes, it is possible to study virus-specific CD8 cells in humans during infection and after vaccination. MHC class I tetramers was used to detect the frequency of haemagglutinin (HA)-specific T cells in 26 healthy influenza-vaccinated humans. Peripheral blood was collected before, and 7, 14 and 28 days after vaccination. Four-colour flow cytometry was used for monitoring of vaccine induced T-cell response. In 15 donors, two- to fivefold increase in frequency of HA-specific T cells was observed 7 days after vaccination. In addition, in 12 of these donors, this increase was accompanied with fourfold increase of H1N1 antibody titre. The increase in frequency of HA-specific CD8⁺/IFN-γ⁺ cells was low and peaked 28 days after vaccination in three of the six donors tested. Frequencies of HA-specific CD8⁺ T cells and antibody titre returned to prevaccination values 1 year after vaccination. Subunit influenza vaccines have the ability to induce HA-specific CD8⁺ cells. As the immune response to this vaccine decreased significantly after 1 year, our results confirm the importance of annual immunization for adequate protection. |
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Bibliography: | http://dx.doi.org/10.1111/j.1365-3083.2007.02042.x ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0300-9475 1365-3083 |
DOI: | 10.1111/j.1365-3083.2007.02042.x |