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Acute inflammatory cardiomyopathy: apparent neutral prognostic impact of immunosuppressive therapy.急性炎症性心肌病:免疫抑制治疗明显的中性预后影响。
Eur J Heart Fail. 2020 Jul;22(7):1280-1282. doi: 10.1002/ejhf.1821. Epub 2020 Apr 15.
2
Myocardial localization of coronavirus in COVID-19 cardiogenic shock.COVID-19 心原性休克中冠状病毒的心肌定位。
Eur J Heart Fail. 2020 May;22(5):911-915. doi: 10.1002/ejhf.1828. Epub 2020 Apr 11.
3
Cardiac Involvement in a Patient With Coronavirus Disease 2019 (COVID-19).新冠肺炎(COVID-19)患者的心脏受累。
JAMA Cardiol. 2020 Jul 1;5(7):819-824. doi: 10.1001/jamacardio.2020.1096.
4
Viral genome search in myocardium of patients with fulminant myocarditis.暴发性心肌炎患者心肌组织中病毒基因组的检测
Eur J Heart Fail. 2020 Jul;22(7):1277-1280. doi: 10.1002/ejhf.1738. Epub 2020 Jan 11.
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Recognition and Initial Management of Fulminant Myocarditis: A Scientific Statement From the American Heart Association.暴发性心肌炎的识别和初步处理:美国心脏协会的科学声明。
Circulation. 2020 Feb 11;141(6):e69-e92. doi: 10.1161/CIR.0000000000000745. Epub 2020 Jan 6.
6
Efficacy and safety of mycophenolate mofetil in patients with virus-negative lymphocytic myocarditis: A prospective cohort study.霉酚酸酯治疗病毒阴性淋巴细胞性心肌炎患者的疗效和安全性:一项前瞻性队列研究。
J Autoimmun. 2020 Jan;106:102330. doi: 10.1016/j.jaut.2019.102330. Epub 2019 Sep 3.
7
Immunosuppression in inflammatory cardiomyopathy and parvovirus B19 persistence.炎症性心肌病中的免疫抑制与细小病毒B19持续感染
Eur J Heart Fail. 2019 Nov;21(11):1468-1469. doi: 10.1002/ejhf.1560. Epub 2019 Sep 2.
8
Survival and Left Ventricular Function Changes in Fulminant Versus Nonfulminant Acute Myocarditis.暴发性与非暴发性急性心肌炎的生存和左心室功能变化。
Circulation. 2017 Aug 8;136(6):529-545. doi: 10.1161/CIRCULATIONAHA.117.026386. Epub 2017 Jun 2.
9
Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis.表现为急性心肌炎的常染色体隐性遗传性心肌病
J Am Coll Cardiol. 2017 Apr 4;69(13):1653-1665. doi: 10.1016/j.jacc.2017.01.043.
10
The Quest for New Approaches in Myocarditis and Inflammatory Cardiomyopathy.探寻心肌炎和炎症性心肌病的新方法。
J Am Coll Cardiol. 2016 Nov 29;68(21):2348-2364. doi: 10.1016/j.jacc.2016.09.937.

病毒存在指导下的淋巴细胞性心肌炎免疫调节:最新进展。

Viral presence-guided immunomodulation in lymphocytic myocarditis: an update.

机构信息

Center for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department, Azienda Sanitaria Universitaria Integrata (ASUITS), University of Trieste, Trieste, Italy.

Center for Diagnosis and Treatment of Cardiomyopathies, Cardiothoracic Department, Institute of Pathological Anatomy and Histology, Azienda Sanitaria Universitaria Integrata (ASUITS), University of Trieste, Trieste, Italy.

出版信息

Eur J Heart Fail. 2021 Feb;23(2):211-216. doi: 10.1002/ejhf.1969. Epub 2020 Aug 20.

DOI:10.1002/ejhf.1969
PMID:32683758
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7405140/
Abstract

Latest statements from European and American societies recommend to rule out viral presence in endomyocardial biopsy (EMB) via polymerase chain reaction (PCR) analysis before starting immunosuppression or immunomodulation in acute lymphocytic myocarditis presenting with life-threatening scenarios. However, recommendations in myocarditis are mostly based on heterogeneous studies enrolling patients with inflammatory cardiomyopathies and established heart failure rather than acute myocarditis. Thus, definitive evidence of a survival benefit from immunomodulation guided by viral presence is currently lacking. Finally, distinguishing innocent bystanders from causative agents among EMB-detected viruses remain challenging and a major goal to achieve in the near future. Therefore, considerable divergence remains between official recommendations and clinical practice, including the possibility of starting immunosuppressive therapy empirically, without knowing viral PCR results. This review systematically discusses the unsolved issues of immunomodulation guided by viral presence in acute lymphocytic myocarditis, namely (i) virus epidemiology and prognosis, (ii) variability of viral presence rates, (iii) the role of potential viral bystander findings, and (iv) the main results of immunosuppression controlled trials in lymphocytic myocarditis. Furthermore, a practical approach for the critical use of viral presence analysis in guiding immunomodulation is provided, highlighting its importance before starting immunosuppression or immunomodulation. Future, multicentre studies are needed to address specific scenarios such as fulminant lymphocytic myocarditis and a virus-tailored management as for parvovirus B19.

摘要

最新的欧美学会声明建议,在开始免疫抑制或免疫调节治疗危及生命的急性淋巴细胞性心肌炎之前,通过聚合酶链反应(PCR)分析排除心肌活检(EMB)中的病毒存在。然而,心肌炎的推荐主要基于异质性研究,这些研究纳入了炎症性心肌病和已确诊心力衰竭的患者,而不是急性心肌炎患者。因此,目前缺乏病毒存在指导免疫调节的生存获益的明确证据。最后,区分心肌活检中检测到的病毒中的无辜旁观者和致病因素仍然具有挑战性,这是近期的主要目标。因此,官方建议和临床实践之间仍然存在相当大的分歧,包括在不知道病毒 PCR 结果的情况下,凭经验开始免疫抑制治疗的可能性。本综述系统地讨论了急性淋巴细胞性心肌炎中病毒存在指导免疫调节的未解决问题,即(i)病毒流行病学和预后,(ii)病毒存在率的可变性,(iii)潜在病毒旁观者发现的作用,以及(iv)淋巴细胞性心肌炎的免疫抑制对照试验的主要结果。此外,还提供了一种在指导免疫调节方面批判性使用病毒存在分析的实用方法,强调了在开始免疫抑制或免疫调节之前其重要性。未来需要开展多中心研究,以解决暴发性淋巴细胞性心肌炎和病毒靶向治疗等特定情况。