Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Department of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Int J Mol Sci. 2020 Aug 4;21(15):5570. doi: 10.3390/ijms21155570.
Vitamin A is an important regulator of immune protection, but it is often overlooked in studies of infectious disease. Vitamin A binds an array of nuclear receptors (e.g., retinoic acid receptor, peroxisome proliferator-activated receptor, retinoid X receptor) and influences the barrier and immune cells responsible for pathogen control. Children and adults in developed and developing countries are often vitamin A-deficient or insufficient, characteristics associated with poor health outcomes. To gain a better understanding of the protective mechanisms influenced by vitamin A, we examined immune factors and epithelial barriers in vitamin A deficient (VAD) mice, vitamin D deficient (VDD) mice, double deficient (VAD+VDD) mice, and mice on a vitamin-replete diet (controls). Some mice received insults, including intraperitoneal injections with complete and incomplete Freund's adjuvant (emulsified with PBS alone or with DNA + Fus-1 peptide) or intranasal inoculations with Sendai virus (SeV). Both before and after insults, the VAD and VAD+VDD mice exhibited abnormal serum immunoglobulin isotypes (e.g., elevated IgG2b levels, particularly in males) and cytokine/chemokine patterns (e.g., elevated eotaxin). Even without insult, when the VAD and VAD+VDD mice reached 3-6 months of age, they frequently exhibited opportunistic ascending bacterial urinary tract infections. There were high frequencies of nephropathy (squamous cell hyperplasia of the renal urothelium, renal scarring, and ascending pyelonephritis) and death in the VAD and VAD+VDD mice. When younger VAD mice were infected with SeV, the predominant lesion was squamous cell metaplasia of respiratory epithelium in lungs and bronchioles. Results highlight a critical role for vitamin A in the maintenance of healthy immune responses, epithelial cell integrity, and pathogen control.
维生素 A 是免疫保护的重要调节剂,但在传染病研究中经常被忽视。维生素 A 结合一系列核受体(如视黄酸受体、过氧化物酶体增殖物激活受体、视黄醇 X 受体),并影响负责控制病原体的屏障和免疫细胞。发达国家和发展中国家的儿童和成人通常存在维生素 A 缺乏或不足的情况,这与健康状况不佳有关。为了更好地了解维生素 A 影响的保护机制,我们研究了维生素 A 缺乏(VAD)小鼠、维生素 D 缺乏(VDD)小鼠、双重缺乏(VAD+VDD)小鼠和维生素充足饮食(对照)的免疫因子和上皮屏障。一些小鼠接受了刺激,包括腹腔内注射完全和不完全弗氏佐剂(单独用 PBS 乳化或与 DNA+Fus-1 肽乳化)或鼻内接种仙台病毒(SeV)。在刺激之前和之后,VAD 和 VAD+VDD 小鼠表现出异常的血清免疫球蛋白同型(例如,IgG2b 水平升高,尤其是雄性)和细胞因子/趋化因子模式(例如,嗜酸性粒细胞趋化因子升高)。即使没有刺激,当 VAD 和 VAD+VDD 小鼠达到 3-6 个月大时,它们经常发生机会性上行细菌性尿路感染。VAD 和 VAD+VDD 小鼠的肾病(肾尿路上皮的鳞状细胞增生、肾瘢痕和上行肾盂肾炎)和死亡率很高。当较年轻的 VAD 小鼠感染 SeV 时,主要病变是肺部和细支气管呼吸上皮的鳞状细胞化生。结果强调了维生素 A 在维持健康免疫反应、上皮细胞完整性和控制病原体方面的关键作用。