首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Prophylactic DNA vaccine for hepatitis C virus (HCV) infection: HCV-specific cytotoxic T lymphocyte induction and protection from HCV-recombinant vaccinia infection in an HLA-A2.1 transgenic mouse model
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Prophylactic DNA vaccine for hepatitis C virus (HCV) infection: HCV-specific cytotoxic T lymphocyte induction and protection from HCV-recombinant vaccinia infection in an HLA-A2.1 transgenic mouse model

机译:丙型肝炎病毒(HCV)感染的预防性DNA疫苗:在HLA-A2.1转基因小鼠模型中HCV特异性细胞毒性T淋巴细胞的诱导和对HCV重组牛痘感染的保护

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摘要

DNA vaccines express antigens intracellularly and effectively induce cellular immune responses. Because only chimpanzees can be used to model human hepatitis C virus (HCV) infections, we developed a small-animal model using HLA-A2.1-transgenic mice to test induction of HLA-A2.1-restricted cytotoxic T lymphocytes (CTLs) and protection against recombinant vaccinia expressing HCV-core. A plasmid encoding the HCV-core antigen induced CD8+ CTLs specific for three conserved endogenously expressed core peptides presented by human HLA-A2.1. When challenged, DNA-immunized mice showed a substantial (5–12 log10) reduction in vaccinia virus titer compared with mock-immunized controls. This protection, lasting at least 14 mo, was shown to be mediated by CD8+ cells. Thus, a DNA vaccine expressing HCV-core is a potential candidate for a prophylactic vaccine for HLA-A2.1+ humans.
机译:DNA疫苗可在细胞内表达抗原并有效诱导细胞免疫应答。由于仅黑猩猩可用于模拟人类丙型肝炎病毒(HCV)感染,因此我们使用HLA-A2.1转基因小鼠开发了小动物模型,以测试诱导HLA-A2.1限制的细胞毒性T淋巴细胞(CTL)和针对表达HCV核心的重组牛痘的保护。编码由HCV-核心抗原诱导的CD8 + CTL的质粒,其对人类HLA-A2.1呈递的三个保守的内源表达核心肽具有特异性。受到挑战时,与模拟免疫对照组相比,经DNA免疫的小鼠显示牛痘病毒滴度显着降低(5-12 log10)。这种保护作用持续至少14 mo,已被CD8 + 细胞介导。因此,表达HCV核心的DNA疫苗可能是预防人类HLA-A2.1 + 的预防性疫苗。

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