Kim Chang H
Laboratory of Immunology and Hematopoiesis, Department of Comparative Pathobiology, Purdue Cancer Center, Purdue University, West Lafayette, IN 47907, USA.
Clin Dev Immunol. 2008;2008:416910. doi: 10.1155/2008/416910.
Vitamin A has both positive and negative regulatory functions in the immune system. While vitamin A is required for normal formation of immune cells and epithelial cell barriers, vitamin A deficiency can lead to increased inflammatory responses and tissue damage. The mechanism with which vitamin A and its metabolites such as retinoids negatively regulate inflammatory responses has not been clearly defined. Recently, it has been established that retinoids promote the generation of immune-suppressive FoxP3+ regulatory T cells while they suppress the T cell differentiation into inflammatory Th17 cells in the periphery such as intestine. These novel functions of retinoids provide a potentially important immune regulatory mechanism. In this review, we discuss the functions of retinoids in the development of the FoxP3+ cells and Th17 cells, the phenotype and functions of retinoid-induced FoxP3+ T cells, and the impact of retinoid-induced FoxP3+ T cells on the immune tolerance.
维生素A在免疫系统中具有正负两方面的调节功能。虽然免疫细胞和上皮细胞屏障的正常形成需要维生素A,但维生素A缺乏会导致炎症反应增加和组织损伤。维生素A及其代谢产物如类视黄醇对炎症反应进行负调节的机制尚未明确。最近,已证实类视黄醇可促进免疫抑制性FoxP3+调节性T细胞的生成,同时在外周组织如肠道中抑制T细胞分化为炎性Th17细胞。类视黄醇的这些新功能提供了一种潜在的重要免疫调节机制。在本综述中,我们讨论了类视黄醇在FoxP3+细胞和Th17细胞发育中的功能、类视黄醇诱导的FoxP3+ T细胞的表型和功能,以及类视黄醇诱导的FoxP3+ T细胞对免疫耐受的影响。