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        <datestamp>2026-09-22T13:08:33Z</datestamp>
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          <dc:title>Table 1_A recombinant Newcastle disease virus-vectored multi-epitope vaccine confers protection against QX-like infectious bronchitis virus in chickens.docx</dc:title>
          <dc:creator>Fei Wang (19534)</dc:creator>
          <dc:creator>Jianan Xie (19256932)</dc:creator>
          <dc:creator>Guoyuan Wen (3474530)</dc:creator>
          <dc:creator>Xusheng Qiu (453653)</dc:creator>
          <dc:creator>Yang Qu (681035)</dc:creator>
          <dc:creator>Yingjie Sun (849052)</dc:creator>
          <dc:creator>Cuiping Song (849051)</dc:creator>
          <dc:creator>Ying Liao (335547)</dc:creator>
          <dc:creator>Chan Ding (317445)</dc:creator>
          <dc:creator>Shunlin Hu (849053)</dc:creator>
          <dc:creator>Lei Tan (211429)</dc:creator>
          <dc:subject>Genetic Immunology</dc:subject>
          <dc:subject>immune-protection</dc:subject>
          <dc:subject>infectious bronchitis virus</dc:subject>
          <dc:subject>multi-epitope vaccine</dc:subject>
          <dc:subject>Newcastle disease virus</dc:subject>
          <dc:subject>QX-like genotype</dc:subject>
          <dc:subject>vaccine vector</dc:subject>
          <dc:description>&lt;p&gt;Infectious bronchitis virus (IBV) QX-like (GI-19) genotype dominates global poultry flocks, yet Mass-type vaccines fail to confer cross-protection. We developed a recombinant Newcastle disease virus (NDV) LaSota vector expressing conserved IBV S1 B-cell hotspots paired with S1-derived BF2-restricted CTL epitopes (rNDV-IBV-T/B). Specific-pathogen-free chickens received single or booster ocular-nasal immunization (10&lt;sup&gt;6&lt;/sup&gt; EID&lt;sub&gt;50&lt;/sub&gt;) followed by QX-like challenge. Booster immunization increased the frequency of splenic CD3&lt;sup&gt;+&lt;/sup&gt;CD8&lt;sup&gt;+&lt;/sup&gt; T cells (41.3% vs. 31.9% in the sham-vaccinated challenge control; Tukey-adjusted p&lt;0.001) and elicited neutralizing antibodies (peak log&lt;sub&gt;2&lt;/sub&gt; GMT, 5.80). Vaccinated groups showed markedly reduced clinical scores, preserved tracheal ciliary activity at all assessed post-challenge time points, and mitigated histopathological lesions. Vaccination reduced oropharyngeal and cloacal viral RNA shedding at multiple post-challenge time points, with the booster regimen producing a more consistent reduction in cloacal viral RNA. Protection was accompanied by an increased frequency of splenic CD3&lt;sup&gt;+&lt;/sup&gt;CD8&lt;sup&gt;+&lt;/sup&gt; T cells, particularly after booster immunization, suggesting a role for cellular immunity alongside neutralizing antibodies. The NDV-LaSota backbone functions as a modular platform for rapid vaccine redesign against emerging coronavirus variants.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-22T13:08:33Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fimmu.2026.1949497.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Table_1_A_recombinant_Newcastle_disease_virus-vectored_multi-epitope_vaccine_confers_protection_against_QX-like_infectious_bronchitis_virus_in_chickens_docx/33965056</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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