Scheerlinck J Y
Centre for Animal Biotechnology, The University of Melbourne, Victoria 3010, Melbourne, Australia.
Vaccine. 2001 Mar 21;19(17-19):2647-56. doi: 10.1016/s0264-410x(00)00495-3.
The relatively low efficacy of DNA vaccines in inducing immune responses, especially in large animal species and humans, has impaired their practical use. Despite considerable effort expended on improving DNA vaccine delivery, only minute amounts of Ag are available for immune induction following DNA vaccination. Two complementary strategies have been used to improve and modulate the immune response induced by DNA vaccines: (i) supplementing DNA vaccines with plasmids encoding cytokines and (ii) targeting the Ag encoded by DNA vaccine through genetically fusing the Ag to molecules binding cell surface receptors. This paper reviews recent progress in these two areas and possible mechanisms responsible for the observed effects.
DNA疫苗在诱导免疫反应方面相对较低的效力,尤其是在大型动物和人类中,已经阻碍了它们的实际应用。尽管在改进DNA疫苗递送方面付出了巨大努力,但DNA疫苗接种后仅有微量的抗原可用于免疫诱导。已采用两种互补策略来改善和调节DNA疫苗诱导的免疫反应:(i)用编码细胞因子的质粒补充DNA疫苗,以及(ii)通过将抗原与结合细胞表面受体的分子进行基因融合来靶向DNA疫苗编码的抗原。本文综述了这两个领域的最新进展以及导致观察到的效应的可能机制。