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Immunogenicity of a Recombinant Influenza Virus Bearing Both the CD4+ and CD8+ T Cell Epitopes of Ovalbumin

机译:携带卵清蛋白的CD4 +和CD8 + T细胞表位的重组流感病毒的免疫原性

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摘要

Recombinant influenza viruses that bear the single immunodominant CD8+ T cell epitope OVA_(257-264) or the CD4+ T cell epitope OVA_(323-339) of the model antigen ovalbumin (OVA) have been useful tools in immunology. Here, we generated a recombinant influenza virus, WSN-OVA_(I-II), that bears both OVA-specific CD8+ and CD4+ epitopes on its hemagglutinin molecule. Live and heat-inactivated WSN-OVA_(I-II) viruses were efficiently presented by dendritic cells in vitro to OT-I TCR transgenic CD8+ T cells and OT-II TCR transgenic CD4+ T cells. In vivo, WSN-OVA_(I-II) virus was attenuated in virulence, highly immunogenic, and protected mice from B16-OVA tumor challenge in a prophylactic model of vaccination. Thus, WSN-OVA_(I-II) virus represents an additional tool, along with OVA TCR transgenic mice, for further studies on T cell responses and may be of value in vaccine design.
机译:带有模型抗原卵清蛋白(OVA)的单个免疫优势CD8 + T细胞表位OVA_(257-264)或CD4 + T细胞表位OVA_(323-339)的重组流感病毒已成为免疫学中的有用工具。在这里,我们生成了重组流感病毒WSN-OVA_(I-II),该病毒在其血凝素分子上同时具有OVA特异性CD8 +和CD4 +表位。树突状细胞在体外有效地将活和热灭活的WSN-OVA_(I-II)病毒呈递给OT-I TCR转基因CD8 + T细胞和OT-II TCR转基因CD4 + T细胞。在体内,在疫苗预防模型中,WSN-OVA_(I-II)病毒的毒力,高度免疫原性和受保护小鼠免受B16-OVA肿瘤攻击的程度有所减弱。因此,WSN-OVA_(I-II)病毒与OVA TCR转基因小鼠一起代表了另一种工具,可用于进一步研究T细胞反应,并且可能在疫苗设计中具有价值。

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