High Fat Low Carbohydrate Diet Is Linked to CNS Autoimmunity Protection

实验性自身免疫性脑脊髓炎 多发性硬化 神经炎症 免疫系统 自身免疫 自身免疫性疾病 免疫学 表型 中枢神经系统 炎症 疾病 医学 生物 内分泌学 内科学 生物化学 抗体 基因
作者
Duan Ni,Jian Tan,Julen Gabirel Araneta Reyes,Alistair M. Senior,Caitlin Andrews,Jemma Taitz,Camille Potier‐Villette,Claire L. Wishart,Alanna G. Spiteri,Laura Piccio,Nicholas J. C. King,Romain Barrès,David Raubenheimer,Stephen J. Simpson,Ralph Nanan,Laurence Macia
出处
期刊:Advanced Science [Wiley]
标识
DOI:10.1002/advs.202412236
摘要

Abstract Multiple sclerosis (MS) is an inflammatory and neurodegenerative disease of the central nervous system (CNS) believed to be driven by autoimmune mechanisms. Genetic and environmental factors are implicated in MS development, and among the latter, diets and nutrients are emerging as potential critical contributors. However, a comprehensive understanding of their impacts and the underlying mechanisms involved is lacking. Harnessing state‐of‐the‐art nutritional geometry analytical methods, it is first revealed that globally, increased carbohydrate supply is associated with increased MS disease burden, while fat supply has an opposite effect. Furthermore, in a MS mouse model, experimental autoimmune encephalomyelitis (EAE), it is found that an isocaloric diet high in carbohydrate aggravated EAE, while a diet enriched in fat (HF) is fully protective. This is reflected by reduced neuroinflammation and skewing toward anti‐inflammatory phenotypes. The protective effects from the HF diet are multifaceted. Metabolically, HF increased lipid storage in immune cells, correlating with their increased anti‐inflammatory IL‐10 production. Transcriptionally and epigenetically, HF feeding preprogrammed naïve T cells toward a less activated but more tolerogenic phenotype. It is showcased that manipulating diets is a potentially efficient and cost‐effective approach to prevent and/or ameliorate EAE. This exhibits translational potentials for prevention/intervention of MS and possibly other autoimmune diseases.
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