首页> 外文期刊>Cancer gene therapy >Vaccination of fiber-modified adenovirus-transfected dendritic cells to express HER-2|[sol]|neu stimulates efficient HER-2|[sol]|neu-specific humoral and CTL responses and reduces breast carcinogenesis in transgenic mice
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Vaccination of fiber-modified adenovirus-transfected dendritic cells to express HER-2|[sol]|neu stimulates efficient HER-2|[sol]|neu-specific humoral and CTL responses and reduces breast carcinogenesis in transgenic mice

机译:纤维修饰的腺病毒转染的树突状细胞表达HER-2 | [sol] | neu的疫苗可刺激HER-2 | [sol] | neu特异的体液和CTL反应,并减少转基因小鼠的乳癌发生

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HER-2eu transgene-modified dendritic cell (DC)-based vaccines are potent at eliciting HER-2eu-specific antitumor immunity. In this study, we constructed a recombinant adenovirus RGDAdVneu with fiber gene modified by RGD insertion into the viral knob's H1 loop. We transfected DCs with RGDAdVneu, and assessed/compared HER-2eu-specific humoral and cytotoxic T lymphocyte (CTL) responses and antitumor immunity derived from the original AdVneu-transfected DCs (DCneu1) and RGDAdVneu-transfected DCs (DCneu2). We demonstrated that DCneu2 displayed increased HER-2eu expression by 8.3-fold compared to DCneu1. We also demonstrated that DCneu2 vaccination induced stronger HER-2eu-specific humoral and CTL immune responses than DCneu1 vaccination. DCneu2 vaccination protected all the mice from HER-2eu-expressing Tg1-1 tumor cell challenge in wild-type FVB/NJ mice, compared to a partial protection in DCneu1-immunized mice. In addition, DCneu2 vaccination also significantly delayed tumor growth than DCneu1 immunization (PP<0.05). Importantly, DCneu2 vaccine reduced breast carcinogenesis by 9% in Tg mice with self HER-2eu tolerance. Therefore, vaccination of fiber-modified adenovirus-transfected DCs to enhance expression of tumor antigens such as HER-2eu is likely representative of a new direction in DC-based vaccine of breast cancer.
机译:基于HER-2 / neu转基因修饰的树突状细胞(DC)的疫苗有效引发HER-2 / neu特异性抗肿瘤免疫。在这项研究中,我们构建了重组腺病毒RGDAdVneu,其纤维基因通过将RGD插入病毒瘤的H1环中而得以修饰。我们用RGDAdVneu转染DC,并评估/比较了源自原始AdVneu转染的DC(DCneu1)和RGDAdVneu转染的DC(DCneu2)的HER-2 / neu特异性体液和细胞毒性T淋巴细胞(CTL)反应和抗肿瘤免疫。我们证明,DCneu2与DCneu1相比,显示出HER-2 / neu表达增加了8.3倍。我们还证明,DCneu2疫苗比DCneu1疫苗诱导更强的HER-2 / neu特异性体液和CTL免疫应答。与DCneu1免疫小鼠的部分保护相比,DCneu2疫苗接种保护所有小鼠免受野生型FVB / NJ小鼠表达HER-2 / neu的Tg1-1肿瘤细胞攻击。此外,DCneu2疫苗接种也比DCneu1免疫接种显着延迟了肿瘤的生长(PP <0.05)。重要的是,DCneu2疫苗在具有自身HER-2 / neu耐受性的Tg小鼠中将乳腺癌的发生率降低了9%。因此,对纤维修饰的腺病毒转染的DC进行疫苗接种以增强肿瘤抗原(例如HER-2 / neu)的表达可能代表了基于DC的乳腺癌疫苗的新方向。

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