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Dendritic cells in atherosclerotic inflammation: the complexity of functions and the peculiarities of pathophysiological effects

机译:树突状细胞在动脉粥样硬化炎症中:功能的复杂性和病理生理学作用的特殊性

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摘要

Atherosclerosis is considered as a chronic disease of arterial wall, with a strong contribution of inflammation. Dendritic cells (DCs) play a crucial role in the initiation of proatherogenic inflammatory response. Mature DCs present self-antigens thereby supporting differentiation of naïve T cells to effector cells that further propagate atherosclerotic inflammation. Regulatory T cells (Tregs) can suppress proinflammatory function of mature DCs. In contrast, immature DCs are able to induce Tregs and prevent differentiation of naïve T cells to proinflammatory effector T cells by initiating apoptosis and anergy in naïve T cells. Indeed, immature DCs showed tolerogenic and anti-inflammatory properties. Thus, DCs play a double role in atherosclerosis: mature DCs are proatherogenic while immature DCs appear to be anti-atherogenic. Tolerogenic and anti-inflammatory capacity of immature DCs can be therefore utilized for the development of new immunotherapeutic strategies against atherosclerosis.
机译:动脉粥样硬化被认为​​是一种慢性的动脉壁疾病,具有强烈的炎症反应。树突状细胞(DC)在促动脉粥样硬化性炎症反应的启动中起关键作用。成熟的DC会呈现自身抗原,从而支持将幼稚T细胞分化为效应细胞,从而进一步传播动脉粥样硬化炎症。调节性T细胞(Tregs)可以抑制成熟DC的促炎功能。相反,未成熟的DC能够通过引发幼稚T细胞的凋亡和无反应性来诱导Tregs并防止幼稚T细胞分化为促炎性效应T细胞。实际上,不成熟的DC表现出致耐受性和抗炎特性。因此,DC在动脉粥样硬化中起着双重作用:成熟的DC具有促动脉粥样硬化作用,而未成熟的DC则具有抗动脉粥样硬化作用。因此,未成熟DC的致耐受力和抗炎能力可用于开发新的抗动脉粥样硬化的免疫疗法。

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