启动(农业)
抗原
生物
dna疫苗
免疫学
抗原处理
质粒
CD8型
DNA
病毒学
免疫
遗传学
发芽
MHC I级
植物
作者
Mark Howarth,Tim Elliott
标识
DOI:10.1111/j.0105-2896.2004.00141.x
摘要
Summary: The ability of DNA vaccines to provide effective immunological protection against infection and tumors depends on their ability to generate good CD4 + and CD8 + T‐cell responses. Priming of these responses is a property of dendritic cells (DCs), and so the efficacy of DNA‐encoded vaccines is likely to depend on the way in which the antigens they encode are processed by DCs. This processing could either be via the synthesis of the vaccine‐encoded antigen by the DCs themselves or via its uptake by DCs following its synthesis in bystander cells that are unable to prime T cells. These different sources of antigen are likely to engage different antigen‐processing pathways, which are the subject of this review. Understanding how to access different processing pathways in DCs may ultimately aid the rational development of plasmid‐based vaccines to pathogens and to cancer.
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