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首页> 外文期刊>Human vaccines & immunotherapeutics. >A DNA vaccine targeting p42.3 induces protective antitumor immunity via eliciting cytotoxic CD8(+)T lymphocytes in a murine melanoma model
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A DNA vaccine targeting p42.3 induces protective antitumor immunity via eliciting cytotoxic CD8(+)T lymphocytes in a murine melanoma model

机译:靶向p42.3的DNA疫苗通过在鼠黑素瘤模型中引发细胞毒性CD8(+)T淋巴细胞来诱导保护性抗肿瘤免疫。

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The p42.3 gene was recently identified and characterized as having tumor-specific and mitosis phase-dependent expression in many types of cancer. This suggested that p42.3 antigen could be used as a target for vaccines against cancers. In this study, we immunized C57BL/6 mice with a DNA vaccine encoding p42.3. We used intramuscular injection with electroporation, either before or after challenge with tumor B16F10 cells. Vaccination with pcDNA3-p42.3 induced some degree of antitumor effect both therapeutically and prophylactically, as evaluated by the inhibition of tumor growth and decrease in tumor weight. Immunized mice showed a high level of specific cytotoxic activity against the p42.3 protein in vivo and had activated CD8 T cells that secreted IFN-gamma, perforin, and granzyme B in response to stimulation with the antigen in vitro. Thus, this study presents the DNA vaccination against novel tumor target p42.3 as a promising antitumor modality.
机译:最近鉴定出p42.3基因,其特征是在许多类型的癌症中具有肿瘤特异性和有丝分裂期依赖性表达。这表明p42.3抗原可以用作抗癌疫苗的靶标。在这项研究中,我们用编码p42.3的DNA疫苗免疫了C57BL / 6小鼠。在对肿瘤B16F10细胞攻击之前或之后,我们通过肌内注射进行了电穿孔。用pcDNA3-p42.3进行疫苗接种可在治疗和预防方面产生一定程度的抗肿瘤作用,这通过抑制肿瘤生长和减轻肿瘤重量来评估。免疫的小鼠体内对p42.3蛋白表现出高水平的特异性细胞毒活性,并具有激活的CD8 T细胞,这些CD8 T细胞响应体外抗原刺激而分泌IFN-γ,穿孔素和颗粒酶B。因此,这项研究提出了针对新型肿瘤靶标p42.3的DNA疫苗接种,这是一种有前途的抗肿瘤方法。

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