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首页> 外文期刊>Clinical immunology: The official journal of the Clinical Immunology Society >Tumor associated antigen and interleukin-12 mRNA transfected dendritic cells enhance effector function of natural killer cells and antigen specific T-cells.
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Tumor associated antigen and interleukin-12 mRNA transfected dendritic cells enhance effector function of natural killer cells and antigen specific T-cells.

机译:肿瘤相关抗原和白介素12 mRNA转染的树突状细胞增强了自然杀伤细胞和抗原特异性T细胞的效应子功能。

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摘要

Immunotherapy aiming at the combined activation of tumor associated antigen (TAA) specific cytotoxic T lymphocytes (CTL) and Natural Killer (NK) cells may be crucial to eradicate both MHC-I positive and negative tumors. Vaccination with mature dendritic cells (DC) transfected with mRNA encoding for TAA and the pro-inflammatory cytokines interleukin (IL)-12 and IL-18 may increase NK cell and TAA specific CTL activity. We demonstrate here that IL-12 over-expressing human DC induces increased NK cell activation and effector function and confirm the increase in TAA specific CTL by TAA/IL-12 double transfected DC. The effects of IL-18 transfection were limited to phenotypic activation and down-regulation of tissue homing receptors and did not add to the effect of IL-12 on NK cell effector function. In conclusion, co-transfection of TAA and IL-12 mRNA into mature DCs offers a vaccine for the induction of an anti-tumor immune response mediated by CTL and NK effector cells.
机译:旨在联合激活肿瘤相关抗原(TAA)特异性细胞毒性T淋巴细胞(CTL)和自然杀伤(NK)细胞的免疫疗法对于根除MHC-1阳性和阴性肿瘤都可能至关重要。用转染了编码TAA的mRNA的成熟树突状细胞(DC)和促炎性细胞因子白介素(IL)-12和IL-18进行疫苗接种可能会增加NK细胞和TAA的特异性CTL活性。我们在这里证明,IL-12过表达的人DC诱导增加的NK细胞活化和效应子功能,并通过TAA / IL-12双转染的DC证实TAA特异性CTL的增加。 IL-18转染的作用仅限于表型激活和组织归巢受体的下调,而没有增加IL-12对NK细胞效应子功能的作用。总之,将TAA和IL-12 mRNA共转染到成熟的DC中提供了一种疫苗,用于诱导由CTL和NK效应细胞介导的抗肿瘤免疫应答。

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