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Significant Impact of Sequence Variations in the Nucleoprotein on CD8 T Cell-Mediated Cross-Protection against Influenza A Virus Infections

Identifieur interne : 000E23 ( Main/Exploration ); précédent : 000E22; suivant : 000E24

Significant Impact of Sequence Variations in the Nucleoprotein on CD8 T Cell-Mediated Cross-Protection against Influenza A Virus Infections

Auteurs : Weimin Zhong [États-Unis] ; Feng Liu [États-Unis] ; Libo Dong [États-Unis] ; Xiuhua Lu [États-Unis] ; Kathy Hancock [États-Unis] ; Ellis L. Reinherz [États-Unis] ; Jacqueline M. Katz [États-Unis] ; Suryaprakash Sambhara [États-Unis]

Source :

RBID : PMC:2868023

Abstract

Background

Memory CD8 T cells to influenza A viruses are widely detectable in healthy human subjects and broadly cross-reactive for serologically distinct influenza A virus subtypes. However, it is not clear to what extent such pre-existing cellular immunity can provide cross-subtype protection against novel emerging influenza A viruses.

Methodology/Principal Findings

We show in the mouse model that naturally occurring sequence variations of the conserved nucleoprotein of the virus significantly impact cross-protection against lethal disease in vivo. When priming and challenge viruses shared identical sequences of the immunodominant, protective NP366/Db epitope, strong cross-subtype protection was observed. However, when they did not share complete sequence identity in this epitope, cross-protection was considerably reduced. Contributions of virus-specific antibodies appeared to be minimal under these circumstances. Detailed analysis revealed that the magnitude of the memory CD8 T cell response triggered by the NP366/Db variants was significantly lower than those triggered by the homologous NP366/Db ligand. It appears that strict specificity of a dominant public TCR to the original NP366/Db ligand may limit the expansion of cross-reactive memory CD8 T cells to the NP366/Db variants.

Conclusions/Significance

Pre-existing CD8 T cell immunity may provide substantial cross-protection against heterosubtypic influenza A viruses, provided that the priming and the subsequent challenge viruses share the identical sequences of the immunodominant, protective CTL epitopes.


Url:
DOI: 10.1371/journal.pone.0010583
PubMed: 20485501
PubMed Central: 2868023


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<name sortKey="Lu, Xiuhua" sort="Lu, Xiuhua" uniqKey="Lu X" first="Xiuhua" last="Lu">Xiuhua Lu</name>
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<addr-line>Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America</addr-line>
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<wicri:regionArea>Department of Medical Oncology, Dana-Farber Cancer Institute, Department of Medicine, Harvard Medical School, Boston, Massachusetts</wicri:regionArea>
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<wicri:regionArea>Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia</wicri:regionArea>
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<sec>
<title>Background</title>
<p>Memory CD8 T cells to influenza A viruses are widely detectable in healthy human subjects and broadly cross-reactive for serologically distinct influenza A virus subtypes. However, it is not clear to what extent such pre-existing cellular immunity can provide cross-subtype protection against novel emerging influenza A viruses.</p>
</sec>
<sec>
<title>Methodology/Principal Findings</title>
<p>We show in the mouse model that naturally occurring sequence variations of the conserved nucleoprotein of the virus significantly impact cross-protection against lethal disease
<italic>in vivo</italic>
. When priming and challenge viruses shared identical sequences of the immunodominant, protective NP
<sub>366</sub>
/D
<sup>b</sup>
epitope, strong cross-subtype protection was observed. However, when they did not share complete sequence identity in this epitope, cross-protection was considerably reduced. Contributions of virus-specific antibodies appeared to be minimal under these circumstances. Detailed analysis revealed that the magnitude of the memory CD8 T cell response triggered by the NP
<sub>366</sub>
/D
<sup>b</sup>
variants was significantly lower than those triggered by the homologous NP
<sub>366</sub>
/D
<sup>b</sup>
ligand. It appears that strict specificity of a dominant public TCR to the original NP
<sub>366</sub>
/D
<sup>b</sup>
ligand may limit the expansion of cross-reactive memory CD8 T cells to the NP
<sub>366</sub>
/D
<sup>b</sup>
variants.</p>
</sec>
<sec>
<title>Conclusions/Significance</title>
<p>Pre-existing CD8 T cell immunity may provide substantial cross-protection against heterosubtypic influenza A viruses, provided that the priming and the subsequent challenge viruses share the identical sequences of the immunodominant, protective CTL epitopes.</p>
</sec>
</div>
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