Immune Regulation Research Group and Immunology Research Centre, School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, Ireland.
Trends Immunol. 2013 Nov;34(11):521-30. doi: 10.1016/j.it.2013.07.006. Epub 2013 Aug 21.
Adaptive immunity plays a crucial role in natural host defence against pathogens and tumours, and is central to the long-term protective effect of vaccines. It is mediated by T and B cells that are activated through antigen-specific receptors. By contrast, innate immunity responds immediately to infection and damage, and is activated through binding of conserved pathogen or damage-associated molecules to pattern recognition receptors (PRRs) on dendritic cells (DCs) and other innate immunity cell types. Recent studies have demonstrated that the innate immune system also functions to direct the adaptive immune response, not only through antigen presentation but also by providing the key signals for the differentiation of naive CD4+ T cells into functionally distinct T helper (Th) cell subtypes.
适应性免疫在天然宿主防御病原体和肿瘤方面发挥着关键作用,也是疫苗长期保护作用的核心。它由 T 细胞和 B 细胞介导,这些细胞通过抗原特异性受体被激活。相比之下,先天免疫会立即对感染和损伤做出反应,并通过模式识别受体 (PRRs) 与树突状细胞 (DC) 和其他先天免疫细胞类型上的保守病原体或损伤相关分子结合而被激活。最近的研究表明,先天免疫系统还可以指导适应性免疫反应,不仅通过抗原呈递,还通过为幼稚 CD4+T 细胞分化为功能不同的 T 辅助 (Th) 细胞亚群提供关键信号来发挥作用。