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Artery Tertiary Lymphoid Organs: Powerhouses of Atherosclerosis Immunity

机译:动脉三级淋巴器官:动脉粥样硬化免疫力的强国

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摘要

Artery tertiary lymphoid organs (ATLOs) are atherosclerosis-associated lymphoid aggregates with varying degrees of complexity ranging from small T/B-cell clusters to well-structured lymph node-like though unencapsulated lymphoid tissues. ATLOs arise in the connective tissue that surrounds diseased arteries, i.e., the adventitia. ATLOs have been identified in aged atherosclerosis-prone hyperlipidemic apolipoprotein E-deficient (ApoE−/−) mice: they are organized into distinct immune cell compartments, including separate T-cell areas, activated B-cell follicles, and plasma cell niches. Analyses of ATLO immune cell subsets indicate antigen-specific T- and B-cell immune reactions within the atherosclerotic arterial wall adventitia. Moreover, ATLOs harbor innate immune cells, including a large component of inflammatory macrophages, B-1 cells, and an aberrant set of antigen-presenting cells. There is marked neoangiogenesis, irregular lymphangiogenesis, neoformation of high endothelial venules, and de novo synthesis of lymph node-like conduits. Molecular mechanisms of ATLO formation remain to be identified though media vascular smooth muscle cells may adopt features of lymphoid tissue organizer-like cells by expressing lymphorganogenic chemokines, i.e., CXCL13 and CCL21. Although these data are consistent with the view that ATLOs participate in primary T- and B-cell responses against elusive atherosclerosis-specific autoantigens, their specific protective or disease-promoting roles remain to be identified. In this review, we discuss what is currently known about ATLOs and their potential impact on atherosclerosis and make attempts to define challenges ahead.
机译:动脉三级淋巴器官(ATLO)是与动脉粥样硬化相关的淋巴样聚集物,其复杂程度从小T / B细胞簇到结构良好的淋巴结样(尽管未包囊的淋巴样组织)复杂程度不同。 ATLO出现在患病动脉(即外膜)周围的结缔组织中。已在易患老年动脉粥样硬化的高脂血症载脂蛋白E(ApoE -// )小鼠中鉴定出ATLO:它们被组织成不同的免疫细胞区室,包括单独的T细胞区域,活化的B细胞卵泡和浆细胞壁ni。对ATLO免疫细胞亚群的分析表明在动脉粥样硬化动脉壁外膜内的抗原特异性T细胞和B细胞免疫反应。此外,ATLO包含先天免疫细胞,包括炎性巨噬细胞的大部分,B-1细胞和一组异常的抗原呈递细胞。有明显的新血管生成,不规则的淋巴血管生成,高内皮小静脉的新形成以及淋巴结样导管的从头合成。尽管中层血管平滑肌细胞可能通过表达淋巴器官形成趋化因子CXCL13和CCL21而具有淋巴样组织组织样细胞的特征,但ATLO形成的分子机制仍有待确定。尽管这些数据与ATLO参与针对难以捉摸的动脉粥样硬化特异性自身抗原的主要T细胞和B细胞反应的观点相一致,但它们的特定保护或促进疾病的作用仍有待确定。在这篇综述中,我们讨论了目前关于ATLO及其对动脉粥样硬化的潜在影响的已知知识,并尝试定义未来的挑战。

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