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首页> 外文期刊>Vaccine >Development of Th1-mediated CD8+effector T cells by vaccination withepitope peptides encapsulated in pH-sensitive liposomes
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Development of Th1-mediated CD8+effector T cells by vaccination withepitope peptides encapsulated in pH-sensitive liposomes

机译:通过用封装在pH敏感脂质体中的表位肽进行疫苗接种来开发Th1介导的CD8 +效应T细胞

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摘要

There have been many studies for tumor therapy mediated by cytotoxic T lymphocytes (CTL) that recognize tumor-associated antigen. It is: generally accepted that CTL responses are induced when antigen is delivered into the cytosol. The pi-I-sensitive liposomes as vehicles are well known for their capacity to deliver the antigen into the cytosol. In this work, immunization of mice with CTL epitope peptides from Hantaan nucleocapsid protein (M6) or human papilloma virus E7 encapsulated in pH-sensitive liposomes induced effective antigen-specific CTL responses. The CTL responses induced by M6 peptide encapsulated in pH-sensitive: liposomes blocked the formation of tumor mass from Hantaan NP transfected B16 melanoma cells in C57BL/6 mice and delayed the growth of preinoculated melanoma cells. During the blockade of the tumor growth, the CTL response was maintained for at least approximately 6 weeks, and the mice secreted Th1 type cytokines such as IL-2 and IFN-gamma. These results suggested that the pH-sensitive liposomes might provide an effective peptide delivery system for CTL-mediated tumor therapy.
机译:由细胞毒性T淋巴细胞(CTL)介导的识别肿瘤相关抗原的肿瘤治疗已有许多研究。公认的是,当抗原被递送到细胞质中时,会诱导CTL反应。作为载体的pi-I敏感脂质体将抗原递送到细胞质中的能力众所周知。在这项工作中,用来自封装在pH敏感脂质体中的汉坦核衣壳蛋白(M6)或人乳头瘤病毒E7的CTL表位肽对小鼠进行免疫,可诱导有效的抗原特异性CTL反应。由封装在pH敏感的M6肽中诱导的CTL响应:脂质体阻止了汉坦NP转染的C16BL / 6小鼠B16黑色素瘤细胞中肿瘤块的形成,并延迟了预先接种的黑色素瘤细胞的生长。在阻止肿瘤生长的过程中,CTL反应至少维持约6周,并且小鼠分泌Th1型细胞因子,例如IL-2和IFN-γ。这些结果表明,pH敏感脂质体可能为CTL介导的肿瘤治疗提供有效的肽传递系统。

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