The bidirectional immune crosstalk in metabolic dysfunction-associated steatotic liver disease

被引:17
|
作者
Sawada, Keisuke [1 ,2 ,4 ,5 ]
Chung, Hak [1 ,2 ]
Softic, Samir [6 ,7 ]
Moreno-Fernandez, Maria E. [1 ,3 ]
Divanovic, Senad [1 ,2 ,4 ,5 ,8 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH 45220 USA
[2] Cincinnati Childrens Hosp Med Ctr, Div Immunobiol, Cincinnati, OH 45229 USA
[3] Cincinnati Childrens Hosp Med Ctr, Div Gastroenterol Hepatol & Nutr, Cincinnati, OH 45229 USA
[4] Univ Cincinnati, Coll Med, Immunol Grad Program, Cincinnati, OH 45220 USA
[5] Univ Cincinnati, Coll Med, Med Scientist Training Program, Cincinnati, OH 45220 USA
[6] Univ Kentucky, Dept Pediat & Gastroenterol, Lexington, KY 40536 USA
[7] Univ Kentucky, Dept Pharmacol & Nutr Sci, Lexington, KY 40536 USA
[8] Cincinnati Childrens Hosp Med Ctr, Ctr Inflammat & Tolerance, Cincinnati, OH 45229 USA
关键词
NONALCOHOLIC FATTY LIVER; CELL-ACTIVATING FACTOR; ADIPOSE-TISSUE INFLAMMATION; NATURAL-KILLER-CELLS; PLASMACYTOID DENDRITIC CELLS; T-CELL; HEPATIC STEATOSIS; B-CELLS; INSULIN-RESISTANCE; CHOLINE-DEFICIENT;
D O I
10.1016/j.cmet.2023.10.009
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Metabolic dysfunction-associated steatotic liver disease (MASLD) is an unabated risk factor for end-stage liver diseases with no available therapies. Dysregulated immune responses are critical culprits of MASLD pathogenesis. Independent contributions from either the innate or adaptive arms of the immune system or their unidirectional interplay are commonly studied in MASLD. However, the bidirectional communication be-tween innate and adaptive immune systems and its impact on MASLD remain insufficiently understood. Given that both innate and adaptive immune cells are indispensable for the development and progression of inflammation in MASLD, elucidating pathogenic contributions stemming from the bidirectional interplay between these two arms holds potential for development of novel therapeutics for MASLD. Here, we review the immune cell types and bidirectional pathways that influence the pathogenesis of MASLD and highlight potential pharmacologic approaches to combat MASLD based on current knowledge of this bidirectional crosstalk.
引用
收藏
页码:1852 / 1871
页数:20
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