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A recombinant E. coli vaccine to promote MHC class I-dependent antigen presentation: application to cancer immunotherapy.

机译:一种重组大肠杆菌疫苗,可促进MHC I类依赖抗原的呈递:应用于癌症免疫治疗。

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We have examined the potential of recombinant Escherichia coli expressing listeriolysin O (LLO) to deliver tumour antigens to dendritic cells (DCs) for cancer immunotherapy. Using OVA as a model tumour antigen, we have shown in murine DCs that E. coli expressing cytoplasmic LLO and OVA proteins can deliver the OVA K(b)-restricted epitope SIINFEKL for MHC class I presentation. In contrast, when E. coli expressing OVA alone were used, MHC class II presentation of the OVA 323-339 I-A(b)-restricted peptide was predominant. When injected in vivo, DCs pulsed with E. coli expressing LLO and OVA induced production of cytotoxic T-lymphocytes capable of lysing an OVA-expressing melanoma cell line (B16-OVA) and resulted in suppression of tumour growth following challenge with B16-OVA. Immunisation of mice by direct injection of E. coli LLO/OVA provided a more potent anti-tumour response, resulting in complete protection in 75% of mice. Injection of live bacteria was not necessary as immunisation with paraformaldehyde-fixed E. coli LLO/OVA provided an even stronger anti-tumour response against B16-OVA. Altogether, our data highlight the potential of this system as a novel and efficient strategy for tumour immunotherapy. doi:10.1038/sj.gt.3301812
机译:我们已经检查了表达李斯特菌溶血素O(LLO)的重组大肠杆菌将肿瘤抗原传递至树突状细胞(DC)进行癌症免疫治疗的潜力。使用OVA作为模型肿瘤抗原,我们已经在鼠类DC中证明表达细胞质LLO和OVA蛋白的大肠杆菌可以递送OVA K(b)限制的抗原决定簇SIINFEKL来进行MHC I类呈递。相反,当使用仅表达OVA的大肠杆菌时,主要是OVA 323-339 I-A(b)限制肽的MHC II类呈递。当在体内注射时,用表达LLO和OVA的大肠杆菌脉冲的DC诱导能够裂解表达OVA的黑色素瘤细胞系(B16-OVA)的细胞毒性T淋巴细胞的产生,并在受到B16-OVA攻击后导致肿瘤生长受到抑制。通过直接注射大肠杆菌LLO / OVA对小鼠进行免疫可提供更有效的抗肿瘤反应,从而对75%的小鼠提供完全保护。不需要注射活菌,因为用低聚甲醛固定的大肠杆菌LLO / OVA免疫可提供针对B16-OVA的更强抗肿瘤反应。总而言之,我们的数据突出了该系统作为肿瘤免疫疗法的一种新颖有效策略的潜力。 doi:10.1038 / sj.gt.3301812

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