IL-15 enhances cross-reactive antibody recall responses to seasonal H3 influenza viruses in vitro
Identifieur interne : 000E56 ( Ncbi/Curation ); précédent : 000E55; suivant : 000E57IL-15 enhances cross-reactive antibody recall responses to seasonal H3 influenza viruses in vitro
Auteurs : Junqiong Huang [République populaire de Chine] ; Shannon P. Hilchey [États-Unis] ; Jiong Wang [États-Unis] ; Jessica Gerigan [États-Unis] ; Martin S. Zand [États-Unis]Source :
- F1000Research [ 2046-1402 ] ; 2017.
Abstract
Url:
DOI: 10.12688/f1000research.12999.1
PubMed: 29479423
PubMed Central: 5801566
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PMC:5801566Le document en format XML
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<italic>in vitro</italic>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">IL-15 enhances cross-reactive antibody recall responses to seasonal H3 influenza viruses
<italic>in vitro</italic>
</title>
<author><name sortKey="Huang, Junqiong" sort="Huang, Junqiong" uniqKey="Huang J" first="Junqiong" last="Huang">Junqiong Huang</name>
<affiliation wicri:level="1"><nlm:aff id="a1">School of Laboratory Medicine, Zunyi Medical University, Zunyi Guizhou, 563099, China</nlm:aff>
<country xml:lang="fr">République populaire de Chine</country>
<wicri:regionArea>School of Laboratory Medicine, Zunyi Medical University, Zunyi Guizhou, 563099</wicri:regionArea>
<wicri:noRegion>563099</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Hilchey, Shannon P" sort="Hilchey, Shannon P" uniqKey="Hilchey S" first="Shannon P." last="Hilchey">Shannon P. Hilchey</name>
<affiliation wicri:level="1"><nlm:aff id="a2">Division of Nephrology, University of Rochester Medical Center, Rochester , NY, 14642, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Division of Nephrology, University of Rochester Medical Center, Rochester , NY, 14642</wicri:regionArea>
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<author><name sortKey="Wang, Jiong" sort="Wang, Jiong" uniqKey="Wang J" first="Jiong" last="Wang">Jiong Wang</name>
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<author><name sortKey="Gerigan, Jessica" sort="Gerigan, Jessica" uniqKey="Gerigan J" first="Jessica" last="Gerigan">Jessica Gerigan</name>
<affiliation wicri:level="1"><nlm:aff id="a2">Division of Nephrology, University of Rochester Medical Center, Rochester , NY, 14642, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Division of Nephrology, University of Rochester Medical Center, Rochester , NY, 14642</wicri:regionArea>
<wicri:noRegion>14642</wicri:noRegion>
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<author><name sortKey="Zand, Martin S" sort="Zand, Martin S" uniqKey="Zand M" first="Martin S." last="Zand">Martin S. Zand</name>
<affiliation wicri:level="1"><nlm:aff id="a2">Division of Nephrology, University of Rochester Medical Center, Rochester , NY, 14642, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Division of Nephrology, University of Rochester Medical Center, Rochester , NY, 14642</wicri:regionArea>
<wicri:noRegion>14642</wicri:noRegion>
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<series><title level="j">F1000Research</title>
<idno type="eISSN">2046-1402</idno>
<imprint><date when="2017">2017</date>
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<front><div type="abstract" xml:lang="en"><p><bold>Background: </bold>
Recently, several human monoclonal antibodies that target conserved epitopes on the stalk region of influenza hemagglutinin (HA) have shown broad reactivity to influenza A subtypes. Also, vaccination with recombinant chimeric HA or stem fragments from H3 influenza viruses induce broad immune protection in mice and humans. However, it is unclear whether stalk-binding antibodies can be induced in human memory B cells by seasonal H3N2 viruses.</p>
<p><bold>Methods:</bold>
In this study, we recruited 13 donors previously exposed to H3 viruses, the majority (12 of 13) of which had been immunized with seasonal influenza vaccines. We evaluated plasma baseline strain-specific and stalk-reactive anti-HA antibodies and B cell recall responses to inactivated H3N2 A/Victoria/361/2011 virus
<italic>in vitro</italic>
using a high throughput multiplex (mPlex-Flu) assay.</p>
<p><bold>Results: </bold>
Stalk-reactive IgG was detected in the plasma of 7 of the subjects. Inactivated H3 viral particles rapidly induced clade cross-reactive antibodies in B cell cultures derived from all 13 donors. In addition, H3 stalk-reactive antibodies were detected in culture supernatants from 7 of the 13 donors (53.8%). H3 stalk-reactive antibodies were also induced by H1 and H7 subtypes. Interestingly, broadly cross-reactive antibody recall responses to H3 strains were also enhanced by stimulating B cells
<italic> in vitro </italic>
with CpG
<sub>2006 </sub>
ODN in the presence of IL-15. H3 stalk-reactive antibodies were detected in CpG
<sub>2006</sub>
ODN + IL-15 stimulated B cell cultures derived from 12 of the 13 donors (92.3%), with high levels detected in cultures from 7 of the 13 donors.</p>
<p><bold>Conclusions:</bold>
Our results demonstrate that stalk-reactive antibody recall responses induced by seasonal H3 viruses and CpG
<sub>2006</sub>
ODN can be enhanced by IL-15.</p>
</div>
</front>
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