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急性和复发性心包炎病理生理学的最新进展。

An update on the pathophysiology of acute and recurrent pericarditis.

机构信息

Division of Cardiology, Department of Internal Medicine, Virginia Commonwealth University, Pauley Heart Center, Richmond, VA, USA -

Department of Internal Medicine, First Clinic of Internal Medicine, University of Genoa, Genoa, Italy -

出版信息

Panminerva Med. 2021 Sep;63(3):249-260. doi: 10.23736/S0031-0808.20.04205-6. Epub 2020 Dec 18.

Abstract

INTRODUCTION

Pericarditis is an inflammatory disease of the pericardium. Progress has been done in recent years in the understanding of its pathophysiology. In particular, preclinical and clinical studies have contributed to increasing our knowledge on the role of interleukin (IL)-1 and NLRP3 (NACHT, leucine-rich repeat, and pyrin domain-containing protein 3) inflammasome.

EVIDENCE ACQUISITION

Information for this study has been retrieved in original articles, reviews, systematic reviews, and meta-analyses identified through PubMed using the following search terms (or combination of terms): "pericarditis," "acute pericarditis," "recurrent pericarditis," "idiopathic recurrent acute pericarditis," "autoimmunity," "autoinflammation," "outcomes." Only articles published in English were included. Additional papers identified from the reference list of the retrieved articles were also considered.

EVIDENCE SYNTHESIS

Based on current evidence, pericarditis should be considered as an inflammatory reaction to various stimuli, including chemical/physical, infectious, or ischemic ones, with a viral infection being a common etiology. Interaction of pathogens or irritants with toll-like receptor (TLRs) and stimulation of IL-1 receptor by IL-1α and IL-1β leads to an increased transcription of proinflammatory genes, including those needed for NLRP3 inflammasome assembly. This pathway is confirmed indirectly by the beneficial effect of colchicine (an indirect NLRP3 inflammasome inhibitor) and IL-1 blockers in patients with recurrent pericarditis. More recently, a direct evidence of the NLRP3 inflammasome within the inflamed pericardium has been provided as well. It may, however, occur that self-antigens on the surface of mesothelial cells or microbial peptides may stimulate autoreactive T cells along with B cells producing antiheart antibodies, although less evidence is available on this.

CONCLUSIONS

Some uncertainties still remain about the role of neutrophils, neutrophil extracellular traps (NETs), and pericardial interstitial cells in recurrent and constrictive pericarditis. Unraveling these aspects might have a direct impact on the development of novel targeted therapies, especially considering the increasing number of drugs targeting NETs.

摘要

简介

心包炎是一种心包的炎症性疾病。近年来,在心包炎的病理生理学方面取得了进展。特别是,临床前和临床研究使我们对白细胞介素 (IL)-1 和 NLRP3(NACHT、富含亮氨酸重复和 pyrin 结构域蛋白 3)炎性体的作用有了更多的了解。

证据获取

通过使用以下搜索词(或搜索词组合)在 PubMed 中检索原始文章、综述、系统综述和荟萃分析,获取了这项研究的信息:“心包炎”、“急性心包炎”、“复发性心包炎”、“特发性复发性急性心包炎”、“自身免疫”、“自身炎症”、“结局”。只纳入发表在英语中的文章。还考虑了从检索到的文章的参考文献中确定的其他论文。

证据综合

根据目前的证据,心包炎应被视为对各种刺激的炎症反应,包括化学/物理、感染或缺血性刺激,病毒感染是常见病因。病原体或刺激物与 toll 样受体 (TLR) 的相互作用以及 IL-1α 和 IL-1β 对 IL-1 受体的刺激导致前炎性基因的转录增加,包括 NLRP3 炎性体组装所需的基因。秋水仙碱(间接 NLRP3 炎性体抑制剂)和 IL-1 阻滞剂在复发性心包炎患者中的有益作用间接证实了这一途径。最近,还提供了炎症性心包内 NLRP3 炎性体的直接证据。然而,可能存在这样的情况,即表面间皮细胞上的自身抗原或微生物肽可能刺激自身反应性 T 细胞和产生抗心脏抗体的 B 细胞,尽管关于这方面的证据较少。

结论

关于中性粒细胞、中性粒细胞胞外陷阱 (NETs) 和心包间质细胞在复发性和缩窄性心包炎中的作用仍存在一些不确定性。阐明这些方面可能会对新型靶向治疗的发展产生直接影响,特别是考虑到针对 NETs 的药物数量不断增加。

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