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        <identifier>oai:figshare.com:article/33979933</identifier>
        <datestamp>2026-09-24T05:33:12Z</datestamp>
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          <dc:title>Table 2_A trivalent gastric cancer antigen conjugated to a diphtheria toxin epitope synergizes with an NKT cell agonist to boost antitumor immunity.xlsx</dc:title>
          <dc:creator>Jing-Jing Du (1973026)</dc:creator>
          <dc:creator>Rong-Ling Liu (25102216)</dc:creator>
          <dc:creator>Yao-Wei Bai (25102219)</dc:creator>
          <dc:creator>Jin-Xuan Su (25102222)</dc:creator>
          <dc:creator>Yuan-Mei Zheng (25102225)</dc:creator>
          <dc:creator>Zhen-Hong Su (20108646)</dc:creator>
          <dc:creator>Shi-Hao Zhou (11994123)</dc:creator>
          <dc:creator>Jun Guo (85069)</dc:creator>
          <dc:creator>Dong-Yuan Wang (20781941)</dc:creator>
          <dc:creator>Ru-Yan Zhang (6443417)</dc:creator>
          <dc:subject>Genetic Immunology</dc:subject>
          <dc:subject>diphtheria toxoid</dc:subject>
          <dc:subject>gastric cancer antigen</dc:subject>
          <dc:subject>NKT cell agonist</dc:subject>
          <dc:subject>peptide vaccine</dc:subject>
          <dc:subject>tumor immunotherapy</dc:subject>
          <dc:description>&lt;p&gt;The gastric cancer-associated antigen MG7-Ag is aberrantly expressed in multiple gastrointestinal malignancies and represents a promising broad-spectrum target for pan-gastrointestinal tumor peptide vaccines; however, its clinical application is hampered by low immunogenicity. To overcome this limitation, we covalently conjugated a diphtheria toxin-derived T-helper epitope to the trivalent antigen MG3, which was constructed by tandem repetition of the monovalent MG1 peptide from the MG7-Ag. A liposomal vaccine was subsequently developed by incorporating DT-MG3 together with the natural killer T (NKT) cell agonist α-galactosylceramide (αGalCer). Immunological evaluation demonstrated that DT-MG3 plus αGalCer elicited significantly higher specific IgG titers than DT-MG3 alone or the unconjugated MG3/αGalCer combination. The vaccine also promoted IFN-γ/IL-4 secretion and boosted CD4&lt;sup&gt;+&lt;/sup&gt;/CD8&lt;sup&gt;+&lt;/sup&gt; T cell responses to elevate antigen immunogenicity. Moreover, the high-titer specific antibodies induced by the vaccine also efficiently bound to EAC tumor cells and induced complement-dependent cytotoxicity. In the EAC ascites model, vaccination with DT-MG3/αGalCer substantially reduced malignant ascites accumulation and prolonged the survival of tumor-bearing mice. Collectively, this novel anti-gastric cancer vaccine based on the covalent conjugation of a diphtheria toxin epitope to the trivalent MG3 antigen, provides valuable insights for the rational design of potent and safe fully synthetic peptide-based anti-tumor vaccines.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-24T05:33:12Z</dc:date>
          <dc:type>Dataset</dc:type>
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          <dc:identifier>10.3389/fimmu.2026.1903458.s001</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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