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首页> 外文期刊>Virology >Codon modified human papillomavirus type 16 E7 DNA vaccine enhances cytotoxic T-lymphocyte induction and anti-tumour activity.
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Codon modified human papillomavirus type 16 E7 DNA vaccine enhances cytotoxic T-lymphocyte induction and anti-tumour activity.

机译:密码子修饰的人乳头瘤病毒16型E7 DNA疫苗增强了细胞毒性T淋巴细胞的诱导和抗肿瘤活性。

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摘要

Polynucleotide immunisation with the E7 gene of human papillomavirus (HPV) type 16 induces only moderate levels of immune response, which may in part be due to limitation in E7 gene expression influenced by biased HPV codon usage. Here we compare for expression and immunogenicity polynucleotide expression plasmids encoding wild-type (pWE7) or synthetic codon optimised (pHE7) HPV16 E7 DNA. Cos-1 cells transfected with pHE7 expressed higher levels of E7 protein than similar cells transfected with pW7. C57BL/6 mice and F1 (C57x FVB) E7 transgenic mice immunised intradermally with E7 plasmids produced high levels of anti-E7 antibody. pHE7 induced a significantly stronger E7-specific cytotoxic T-lymphocyte response than pWE7 and 100% tumour protection in C57BL/6 mice, but neither vaccine induced CTL in partially E7 tolerant K14E7 transgenic mice. The data indicate that immunogenicity of an E7 polynucleotide vaccine can be enhanced by codon modification. However, this may be insufficient for priming E7 responses in animals with split tolerance to E7 as a consequence of expression of E7 in somatic cells.
机译:用人乳头瘤病毒(HPV)16型E7基因进行多核苷酸免疫仅诱导中等水平的免疫反应,这可能部分是由于有偏见的HPV密码子使用对E7基因表达的限制。在这里,我们比较了编码野生型(pWE7)或合成密码子优化(pHE7)HPV16 E7 DNA的表达和免疫原性多核苷酸表达质粒。用pHE7转染的Cos-1细胞表达的E7蛋白水平高于用pW7转染的类似细胞。用E7质粒皮内免疫的C57BL / 6小鼠和F1(C57x FVB)E7转基因小鼠产生了高水平的抗E7抗体。在C57BL / 6小鼠中,pHE7诱导的E7特异性细胞毒性T淋巴细胞应答比pWE7显着强得多,并且100%的肿瘤保护作用,但两种疫苗均未在部分E7耐受的K14E7转基因小鼠中诱导CTL。数据表明E7多核苷酸疫苗的免疫原性可以通过密码子修饰来增强。但是,这可能不足以引发E7反应,因为E7在体细胞中的表达会导致对E7具有不同耐受性的动物。

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