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外周CD4CD25Foxp3调节性T细胞的调节改善了载脂蛋白E缺陷小鼠手术应激诱导的动脉粥样硬化斑块进展。

Modulation of Peripheral CD4CD25Foxp3 Regulatory T Cells Ameliorates Surgical Stress-Induced Atherosclerotic Plaque Progression in ApoE-Deficient Mice.

作者信息

Handke Jessica, Kummer Laura, Weigand Markus A, Larmann Jan

机构信息

Department of Anesthesiology, Heidelberg University Hospital, Heidelberg, Germany.

出版信息

Front Cardiovasc Med. 2021 Aug 12;8:682458. doi: 10.3389/fcvm.2021.682458. eCollection 2021.

Abstract

Systemic inflammation associated with major surgery rapidly accelerates atherosclerotic plaque progression in mice. Regulatory T cells (Tregs) have emerged as important modulators of atherogenesis. In coronary artery disease patients, low frequency of Tregs constitutes an independent risk factor for cardiovascular complications after non-cardiac surgery. In this exploratory analysis, we investigate whether preoperative Treg levels affect surgery-induced atherosclerotic lesion destabilization in a murine model of perioperative stress. After 9 weeks of high-cholesterol diet, atherosclerotic apolipoprotein E-deficient mice with modulated Treg levels were subjected to a 30-minute surgical procedure consisting of general isoflurane anesthesia, laparotomy and moderate blood loss. Controls underwent general anesthesia only. Brachiocephalic arteries were harvested 3 days after the intervention for histomorphological analyses of atherosclerotic plaques. Tregs were depleted by a single dose of anti-CD25 monoclonal antibody (mAb) administered 6 days prior to the intervention. Expansion of Tregs was induced by daily injections of IL-2/anti-IL-2 complex (IL-2C) on three consecutive days starting 3 days before surgery. Isotype-matched antibodies and PBS served as controls. Antibody-mediated modulation was Treg-specific. IL-2C treatment resulted in an eight-fold elevation of peripheral CD4CD25Foxp3 Tregs compared to mice administered with anti-CD25 mAb. In mice treated with PBS and anti-CD25 mAb, surgical stress response caused a significant increase of atherosclerotic plaque necrosis (PBS: < 0.001; anti-CD25 mAb: = 0.037). Preoperative Treg expansion abrogated perioperative necrotic core formation ( = 0.556) and significantly enhanced postoperative atherosclerotic plaque stability compared to PBS-treated mice ( = 0.036). Postoperative plaque volume ( = 0.960), stenosis ( = 0.693), lesional collagen ( = 0.258), as well as the relative macrophage ( = 0.625) and smooth muscle cell content ( = 0.178) remained largely unaffected by preoperative Treg levels. In atherosclerotic mice, therapeutic expansion of Tregs prior to major surgery mitigates rapid effects on perioperative stress-driven atherosclerotic plaque destabilization. Future studies will show, whether short-term interventions modulating perioperative inflammation qualify for prevention of cardiovascular events associated with major non-cardiac surgery.

摘要

与大手术相关的全身炎症会迅速加速小鼠动脉粥样硬化斑块的进展。调节性T细胞(Tregs)已成为动脉粥样硬化发生的重要调节因子。在冠状动脉疾病患者中,Tregs频率低是心脏非手术术后心血管并发症的独立危险因素。在这项探索性分析中,我们研究术前Treg水平是否会影响围手术期应激小鼠模型中手术诱导的动脉粥样硬化病变不稳定。在高胆固醇饮食9周后,对Treg水平被调节的动脉粥样硬化载脂蛋白E缺陷小鼠进行30分钟的手术,包括全身异氟醚麻醉、剖腹术和中度失血。对照组仅接受全身麻醉。干预3天后采集头臂动脉,对动脉粥样硬化斑块进行组织形态学分析。在干预前6天给予单剂量抗CD25单克隆抗体(mAb)以耗尽Tregs。从手术前3天开始连续3天每天注射IL-2/抗IL-2复合物(IL-2C)诱导Tregs扩增。同型匹配抗体和PBS作为对照。抗体介导的调节是Treg特异性的。与给予抗CD25 mAb的小鼠相比,IL-2C治疗使外周CD4CD25Foxp3 Tregs升高了8倍。在用PBS和抗CD25 mAb治疗的小鼠中,手术应激反应导致动脉粥样硬化斑块坏死显著增加(PBS:<0.001;抗CD25 mAb:=0.037)。与PBS处理的小鼠相比,术前Treg扩增消除了围手术期坏死核心的形成(=0.556),并显著增强了术后动脉粥样硬化斑块的稳定性(=0.036)。术后斑块体积(=0.960)、狭窄(=0.693)、病变胶原(=0.258)以及相对巨噬细胞(=0.625)和平滑肌细胞含量(=0.178)在很大程度上不受术前Treg水平的影响。在动脉粥样硬化小鼠中,大手术前Tregs的治疗性扩增减轻了围手术期应激驱动的动脉粥样硬化斑块不稳定的快速影响。未来的研究将表明,调节围手术期炎症的短期干预措施是否符合预防与非心脏大手术相关的心血管事件的条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5140/8416168/b12634b0dab8/fcvm-08-682458-g0001.jpg

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