L Bishop Emma, Ismailova Aiten, Dimeloe Sarah, Hewison Martin, White John H
Institute of Immunology and Immunotherapy University of Birmingham Birmingham UK.
Department of Physiology McGill University Montreal Quebec Canada.
JBMR Plus. 2020 Sep 15;5(1):e10405. doi: 10.1002/jbm4.10405. eCollection 2021 Jan.
Regulation of immune function continues to be one of the most well-recognized extraskeletal actions of vitamin D. This stemmed initially from the discovery that antigen presenting cells such as macrophages could actively metabolize precursor 25-hydroxyvitamin D (25D) to active 1,25-dihydroxyvitamin D (1,25D). Parallel observation that activated cells from the immune system expressed the intracellular vitamin D receptor (VDR) for 1,25D suggested a potential role for vitamin D as a localized endogenous modulator of immune function. Subsequent studies have expanded our understanding of how vitamin D exerts effects on both the innate and adaptive arms of the immune system. At an innate level, intracrine synthesis of 1,25D by macrophages and dendritic cells stimulates expression of antimicrobial proteins such as cathelicidin, as well as lowering intracellular iron concentrations via suppression of hepcidin. By potently enhancing autophagy, 1,25D may also play an important role in combatting intracellular pathogens such as and viral infections. Local synthesis of 1,25D by macrophages and dendritic cells also appears to play a pivotal role in mediating T-cell responses to vitamin D, leading to suppression of inflammatory T helper (Th)1 and Th17 cells, and concomitant induction of immunotolerogenic T-regulatory responses. The aim of this review is to provide an update on our current understanding of these prominent immune actions of vitamin D, as well as highlighting new, less well-recognized immune effects of vitamin D. The review also aims to place this mechanistic basis for the link between vitamin D and immunity with studies in vivo that have explored a role for vitamin D supplementation as a strategy for improved immune health. This has gained prominence in recent months with the global coronavirus disease 2019 health crisis and highlights important new objectives for future studies of vitamin D and immune function. © 2020 The Authors. published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
免疫功能调节一直是维生素D最为人熟知的骨骼外作用之一。这一认识最初源于巨噬细胞等抗原呈递细胞能够将前体25-羟基维生素D(25D)主动代谢为活性1,25-二羟基维生素D(1,25D)的发现。同时观察到免疫系统的活化细胞表达1,25D的细胞内维生素D受体(VDR),这表明维生素D作为免疫功能的局部内源性调节剂具有潜在作用。随后的研究扩展了我们对维生素D如何影响免疫系统的先天性和适应性分支的理解。在先天性层面,巨噬细胞和树突状细胞对1,25D的内分泌合成刺激了抗菌蛋白(如cathelicidin)的表达,并通过抑制铁调素降低细胞内铁浓度。通过有力地增强自噬,1,25D在对抗细胞内病原体(如细菌和病毒感染)方面也可能发挥重要作用。巨噬细胞和树突状细胞对1,25D的局部合成似乎在介导T细胞对维生素D的反应中也起着关键作用,导致炎性辅助性T(Th)1和Th17细胞受到抑制,并伴随免疫耐受性调节性T细胞反应的诱导。本综述的目的是更新我们目前对维生素D这些突出免疫作用的理解,并突出维生素D新的、较少被认识的免疫作用。该综述还旨在将维生素D与免疫之间联系的这一机制基础与体内研究相结合,这些研究探索了补充维生素D作为改善免疫健康策略的作用。在最近几个月,随着全球2019冠状病毒病健康危机的出现,这一点变得尤为突出,并突出了维生素D与免疫功能未来研究的重要新目标。© 2020作者。由Wiley Periodicals LLC代表美国骨与矿物质研究学会出版。