免疫系统
胆固醇逆向转运
炎症
胆固醇
免疫学
脂蛋白
背景(考古学)
自身免疫
生物
ABCA1
内分泌学
内科学
医学
运输机
生物化学
基因
古生物学
作者
Marisa Neves,Joana R. Batuca,José Delgado Alves
出处
期刊:Immunology
[Wiley]
日期:2021-05-02
卷期号:164 (2): 231-241
被引量:19
摘要
Summary Inflammation and immune dysfunction have been increasingly recognized as crucial mechanisms in atherogenesis. Modifications in cell lipid metabolism, plasma dyslipidaemia and particularly low high‐density lipoprotein (HDL) levels occur both in atherosclerosis and in autoimmune rheumatic diseases (which are strongly associated with an increased risk of atherosclerosis), suggesting the presence of a crucial link. HDL, the plasma lipoprotein responsible for reverse cholesterol transport, is known for its several protective effects in the context of atherosclerosis. Among these, HDL immunomodulatory effects are possibly the less understood. Through the efflux of cholesterol from plasma cell membranes with the consequent disruption of lipid rafts and the interaction with the cholesterol transporters present in the plasma membrane, HDL affects both the innate and adaptive immune responses. Animal and human studies have demonstrated a predominance of HDL anti‐inflammatory effects, despite some pro‐inflammatory actions having also been reported. The HDL role on the modulation of the immune response is further suggested by the detection of low levels together with a dysfunctional HDL in patients with autoimmune diseases. Here, we review the current knowledge of the immune mechanisms of atherosclerosis and the modulatory effects HDL may have on them.
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