<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lillie PJ</submitter><funding>Medical Research Council</funding><funding>Wellcome Trust</funding><pagination>19-25</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3369564</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>55(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The novel influenza vaccine MVA-NP+M1 is designed to boost cross-reactive T-cell responses to internal antigens of the influenza A virus that are conserved across all subtypes, providing protection against both influenza disease and virus shedding against all influenza A viruses. Following a phase 1 clinical study that demonstrated vaccine safety and immunogenicity, a phase 2a vaccination and influenza challenge study has been conducted in healthy adult volunteers.&lt;h4>Methods&lt;/h4>Volunteers with no measurable serum antibodies to influenza A/Wisconsin/67/2005 received either a single vaccination with MVA-NP+M1 or no vaccination. T-cell responses to the vaccine antigens were measured at enrollment and again prior to virus challenge. All volunteers underwent intranasal admi</pubmed_abstract><journal>Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</journal><pubmed_title>Preliminary assessment of the efficacy of a T-cell-based influenza vaccine, MVA-NP+M1, in humans.</pubmed_title><pmcid>PMC3369564</pmcid><funding_grant_id>095540</funding_grant_id><funding_grant_id>G1001046</funding_grant_id><funding_grant_id>G0600520</funding_grant_id><funding_grant_id>081865</funding_grant_id><funding_grant_id>090532</funding_grant_id><pubmed_authors>Peng Y</pubmed_authors><pubmed_authors>Dong T</pubmed_authors><pubmed_authors>Lambe T</pubmed_authors><pubmed_authors>Sheehy SH</pubmed_authors><pubmed_authors>Hill AV</pubmed_authors><pubmed_authors>Blais ME</pubmed_authors><pubmed_authors>Gilbert A</pubmed_authors><pubmed_authors>Oxford J</pubmed_authors><pubmed_authors>Gilbert SC</pubmed_authors><pubmed_authors>Spencer AJ</pubmed_authors><pubmed_authors>Hamill M</pubmed_authors><pubmed_authors>Duncan CJ</pubmed_authors><pubmed_authors>Havelock T</pubmed_authors><pubmed_authors>Powell TJ</pubmed_authors><pubmed_authors>Lillie PJ</pubmed_authors><pubmed_authors>Williams RL</pubmed_authors><pubmed_authors>Mullarkey C</pubmed_authors><pubmed_authors>Berthoud TK</pubmed_authors><pubmed_authors>Faust SN</pubmed_authors></additional><is_claimable>false</is_claimable><name>Preliminary assessment of the efficacy of a T-cell-based influenza vaccine, MVA-NP+M1, in humans.</name><description>&lt;h4>Background&lt;/h4>The novel influenza vaccine MVA-NP+M1 is designed to boost cross-reactive T-cell responses to internal antigens of the influenza A virus that are conserved across all subtypes, providing protection against both influenza disease and virus shedding against all influenza A viruses. Following a phase 1 clinical study that demonstrated vaccine safety and immunogenicity, a phase 2a vaccination and influenza challenge study has been conducted in healthy adult volunteers.&lt;h4>Methods&lt;/h4>Volunteers with no measurable serum antibodies to influenza A/Wisconsin/67/2005 received either a single vaccination with MVA-NP+M1 or no vaccination. T-cell responses to the vaccine antigens were measured at enrollment and again prior to virus challenge. All volunteers underwent intranasal admi</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Jul</publication><modification>2026-05-04T20:53:30.618Z</modification><creation>2019-03-27T00:54:15Z</creation></dates><accession>S-EPMC3369564</accession><cross_references><pubmed>22441650</pubmed><doi>10.1093/cid/cis327</doi></cross_references></HashMap>