Immunity at Barrier Sites Initiative, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Disease, NIH, Bethesda 20892, USA.
Science. 2014 Jan 24;343(6169):432-7. doi: 10.1126/science.1247606.
How the immune system adapts to malnutrition to sustain immunity at barrier surfaces, such as the intestine, remains unclear. Vitamin A deficiency is one of the most common micronutrient deficiencies and is associated with profound defects in adaptive immunity. Here, we found that type 3 innate lymphoid cells (ILC3s) are severely diminished in vitamin A-deficient settings, which results in compromised immunity to acute bacterial infection. However, vitamin A deprivation paradoxically resulted in dramatic expansion of interleukin-13 (IL-13)-producing ILC2s and resistance to nematode infection in mice, which revealed that ILCs are primary sensors of dietary stress. Further, these data indicate that, during malnutrition, a switch to innate type 2 immunity may represent a powerful adaptation of the immune system to promote host survival in the face of ongoing barrier challenges.
免疫系统如何适应营养不良以维持肠道等屏障表面的免疫力仍不清楚。维生素 A 缺乏是最常见的微量营养素缺乏症之一,与适应性免疫的严重缺陷有关。在这里,我们发现,在维生素 A 缺乏的情况下,3 型先天淋巴样细胞(ILC3)严重减少,导致对急性细菌感染的免疫力受损。然而,维生素 A 的剥夺却出人意料地导致了白细胞介素 13(IL-13)产生的 ILC2 的剧烈扩张,并使小鼠对线虫感染产生抗性,这表明 ILC 是膳食应激的主要传感器。此外,这些数据表明,在营养不良期间,向先天 2 型免疫的转变可能代表免疫系统的一种强大适应,以促进宿主在持续的屏障挑战面前的生存。