Division of Allergy and Immunology, Department of Medicine, National Jewish Health, Denver, CO 80206, USA.
Immunol Res. 2013 Mar;55(1-3):173-7. doi: 10.1007/s12026-012-8361-z.
Type-2 immune responses are the underlying cause of many allergic diseases and provide protection against parasitic infection. Effective type-2 immune responses are generated by type-2 helper CD4(+) T cells (Th2) as well as type-2 innate effector cells. While we have learned a great deal about how CD4(+) Th2 cells regulate their Th2 cytokine gene transcription, we still do not know how type-2 innate effector cells acquire their capacity to express Th2 cytokine genes. Furthermore, it remains poorly understood how Th2 cytokines regulate the differentiation of innate type-2 progenitor cells. In this review, we will focus on (1) the long distance interaction between the sites of allergic inflammation and the site of hematopoiesis in the bone marrow, (2) the characteristics of innate type-2 progenitors, and (3) the molecular mechanisms by which innate type-2 effector cells acquire the capacity to produce type-2 cytokines.
2 型免疫应答是许多过敏性疾病的根本原因,并为寄生虫感染提供保护。2 型辅助 CD4(+)T 细胞(Th2)以及 2 型先天效应细胞产生有效的 2 型免疫应答。虽然我们已经了解了 CD4(+)Th2 细胞如何调节其 Th2 细胞因子基因转录,但我们仍然不知道 2 型先天效应细胞如何获得表达 Th2 细胞因子基因的能力。此外,Th2 细胞因子如何调节先天 2 型祖细胞的分化仍然知之甚少。在这篇综述中,我们将重点讨论(1)过敏炎症部位与骨髓造血部位之间的长距离相互作用,(2)先天 2 型祖细胞的特征,以及(3)先天 2 型效应细胞获得产生 2 型细胞因子能力的分子机制。