4.3 Article

Adventitial tertiary lymphoid organ classification in human atherosclerosis

期刊

CARDIOVASCULAR PATHOLOGY
卷 32, 期 -, 页码 8-14

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.carpath.2017.08.002

关键词

Adventitial tertiary lymphoid organs; Atherosclerosis; Inflammation

资金

  1. German Research Foundation [ER682/2-1, SFB938/TP Z2]
  2. German Heart Foundation/German Foundation of Heart Research [F/23/12]
  3. German Centre for Cardiovascular Research
  4. German Ministry of Education and Research

向作者/读者索取更多资源

Background: Atherosclerosis is a chronic inflammatory disease of the arterial wall Adjacent to lamina intima lesion progression, a cellular compound develops in the lamina aclventitia, defined as tertiary lymphoid organs (TLO) in mice But in human system, it remains unknown whether these adventitial cellular accumulations represent these highly organized immunological structures. Patients and methods: In this study, we investigated whether the adventitial cellular compounds represent TLOs in 72 human coronary artery samples by immunoenzyme staining. Results: The study showed that the adventitial cellular compound partly represented TLOs in human coronary arteries affected by atherogenesis in patients suffering from ischemic heart disease (56%) or a fatal myocardial infarction (100%), but not dilated cardiomyopathy. In addition, we established a classification for human TLOs, stagel-III, and showed that all stages were present in diseased coronary arteries. The stage of TLOs highly conclated with lesion size as well as plaque instability and rupture, and all patients with a myocardial infarction had stage III. Additionally, there were cellular infiltration and destruction of the lamina media, which were restricted to TLOs next to ruptured plaques in patients with a fatal myocardial infarction. Conclusions: TLOs are present in patients with a coronary artery disease and highly correlated with lesion size, plaque instability, and rupture. Further studies are needed to investigate whether TLOs might be a specific diagnostic and drug target to modify plaque instability rupture. (C) 2017 Elsevier Inc. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据