Immunology Graduate Program, University of Iowa, Iowa City, IA.
Carver College of Medicine, University of Iowa, Iowa City, IA.
Immunohorizons. 2023 Mar 1;7(3):213-227. doi: 10.4049/immunohorizons.2300008.
Multiple sclerosis (MS) is an autoimmune demyelinating disease of the CNS that is linked with both genetic and environmental factors. A Western-style diet rich in fat and simple sugars is hypothesized as a potential factor contributing to the increased incidence of inflammatory autoimmune diseases, such as MS, in developed countries. Although the adverse effects of a high-fat diet in MS have been studied extensively, the effect of a fructose-rich diet (FRD) on MS etiology is unknown. We hypothesized that an FRD will alter the gut microbiome, influence immune populations, and negatively impact disease in experimental autoimmune encephalomyelitis (EAE), an animal model of MS. To test this, we fed C57BL/6 mice either an FRD or normal feed for 4 or 12 wk and analyzed the effect of an FRD on gut microbiota, immune populations, and EAE. An FRD significantly influenced the gut microbiota, with reduced abundance of beneficial bacteria and enrichment of potentially proinflammatory bacteria. We also observed immune modulation in the gut and periphery. Of particular interest was a population of Helios-RORγt+Foxp3+CD4+ T cells that was enriched in the small intestine lamina propria of FRD-fed mice. However, despite gut microbiota and immune modulations, we observed only a subtle effect of an FRD on EAE severity. Overall, our data suggest that in C57Bl6/J mice, an FRD modulates the gut microbiota and immune system without significantly impacting myelin oligodendrocyte glycoprotein 35-55/CFA-induced EAE.
多发性硬化症(MS)是一种中枢神经系统的自身免疫性脱髓鞘疾病,与遗传和环境因素都有关。高脂肪和简单糖的西式饮食被认为是导致发达国家炎症性自身免疫性疾病(如 MS)发病率增加的潜在因素。尽管高脂肪饮食对 MS 的不良影响已被广泛研究,但富含果糖的饮食(FRD)对 MS 病因的影响尚不清楚。我们假设 FRD 会改变肠道微生物群,影响免疫群体,并对实验性自身免疫性脑脊髓炎(EAE)产生负面影响,EAE 是 MS 的动物模型。为了验证这一点,我们用 FRD 或正常饲料喂养 C57BL/6 小鼠 4 或 12 周,并分析 FRD 对肠道微生物群、免疫群体和 EAE 的影响。FRD 显著影响肠道微生物群,有益细菌的丰度降低,潜在促炎细菌的丰度增加。我们还观察到肠道和外周的免疫调节。特别有趣的是,Helios-RORγt+Foxp3+CD4+T 细胞的一个群体在 FRD 喂养小鼠的小肠固有层中富集。然而,尽管肠道微生物群和免疫调节,我们仅观察到 FRD 对 EAE 严重程度的轻微影响。总的来说,我们的数据表明,在 C57Bl6/J 小鼠中,FRD 调节肠道微生物群和免疫系统,而对髓鞘少突胶质细胞糖蛋白 35-55/CFA 诱导的 EAE 没有显著影响。