Cellular and Molecular Links between Autoimmunity and Lipid Metabolism

The incidence of atherosclerosis is higher among patients with several autoimmune diseases such as psoriasis, rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). It is well documented that innate immune cells including macrophages and dendritic cells sense lipid species such as saturat...

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Published inMolecules and cells Vol. 42; no. 11; pp. 747 - 754
Main Authors Ryu, Heeju, Kim, Jiyeon, Kim, Daehong, Lee, Jeong-Eun, Chung, Yeonseok
Format Journal Article
LanguageEnglish
Published United States Korean Society for Molecular and Cellular Biology 01.11.2019
한국분자세포생물학회
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Summary:The incidence of atherosclerosis is higher among patients with several autoimmune diseases such as psoriasis, rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). It is well documented that innate immune cells including macrophages and dendritic cells sense lipid species such as saturated fatty acids and oxidized low-density lipoprotein and produce pro-inflammatory cytokines and chemokines. However, whether a hyperlipidemic environment also impacts autoimmune T cell responses has been unclear. Among CD4+ T cells, Th17 and follicular helper T (Tfh) cells are known to play pathogenic roles in the development of hyperlipidemiaassociated autoimmune diseases. This review gives an overview of the cellular and molecular mechanisms by which dysregulated lipid metabolism impacts the pathogenesis of autoimmune diseases, with specific emphasis on Th17 and Tfh cells.
Bibliography:These authors contributed equally to this work.
http://www.molcells.org/journal/view.html?doi=10.14348/molcells.2019.0196
ISSN:1016-8478
0219-1032
DOI:10.14348/molcells.2019.0196