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在DNA疫苗中,抗原与Fas配体融合可增强免疫原性。

Fusion of antigen to Fas-ligand in a DNA vaccine enhances immunogenicity.

作者信息

Nimal Sonali, Thomas Mark S, Heath Andrew W

机构信息

Unit of Infection and Immunity, University of Sheffield Medical School, Sheffield S10 2RX, UK.

出版信息

Vaccine. 2007 Mar 8;25(12):2306-15. doi: 10.1016/j.vaccine.2006.11.059. Epub 2006 Dec 11.

Abstract

DNA vaccines have considerable potential for the prophylaxis and therapy of a range of diseases, but their potential has not been realised largely due to poor immunogenicity. Fas ligand is a pro-apoptotic molecule, able to induce death of Fas expressing cells. We describe the construction of a DNA vaccine encoding a chimeric fusion between Fas ligand and a truncated version of HIV gp120 as a model antigen. The fusion DNA was used as a priming vaccine, along with boosting with recombinant gp120 protein. Priming with fusion protein DNA resulted in a powerful enhancement of immune responses to the protein boost, and, in the presence of aluminum phosphate, to a strong enhancement in T helper 2 type responses. Fas ligand delivered in a separate plasmid also had an adjuvant effect, although it was weaker than that delivered by the fusion protein.

摘要

DNA疫苗在一系列疾病的预防和治疗方面具有相当大的潜力,但其潜力尚未得到充分发挥,主要原因是免疫原性较差。Fas配体是一种促凋亡分子,能够诱导表达Fas的细胞死亡。我们描述了一种DNA疫苗的构建,该疫苗编码Fas配体与HIV gp120截短形式之间的嵌合融合体作为模型抗原。融合DNA用作初免疫苗,并与重组gp120蛋白加强免疫。用融合蛋白DNA进行初免可显著增强对蛋白加强免疫的免疫反应,并且在存在磷酸铝的情况下,可强烈增强2型辅助性T细胞反应。单独质粒递送的Fas配体也具有佐剂作用,尽管其作用比融合蛋白递送的弱。

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