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致命免疫球蛋白:自身抗体与心源性猝死。

Lethal immunoglobulins: Autoantibodies and sudden cardiac death.

机构信息

Laboratory of the Mosaics of Autoimmunity, Saint Petersburg State University, Saint-Petersburg, Russian Federation.

Saint Petersburg State University, Saint-Petersburg, Russian Federation.

出版信息

Autoimmun Rev. 2019 Apr;18(4):415-425. doi: 10.1016/j.autrev.2018.12.005. Epub 2019 Feb 14.

DOI:10.1016/j.autrev.2018.12.005
PMID:30772491
Abstract

Sudden cardiac death (SCD) is an unexpected death due to cardiac causes that occurs in a short time period (generally within 1 h of symptom onset) in a person with known or unknown cardiac disease. Patients with cardiomyopathies, myocarditis, ischemic heart disease and cardiac channelopathies are at risk of SCD. However, a certain percentage of autopsy-negative cases of SCD in the young (<35 years) remain unexplained even after a post-mortem genetic testing. Autoantibodies against cardiac proteins may be potentially involved in the pathogenesis of different heart diseases and in the occurrence of unexplained SCD. In this review we analyze clinical and animal studies that elucidate the prevalence of these autoantibodies in patients with different cardiac diseases and their pathophysiological relevance. We propose a classification of the autoantibodies associated with heart diseases and focus on their molecular and cellular effects. Anti-beta adrenergic receptor antibodies and anti-muscarinic acetylcholine receptor antibodies affect myocardial electrophysiological properties and were reported to be the independent predictors of SCD in patients with different heart diseases. Autoimmune mechanism is proposed for cardiac-related adverse reactions following human papillomavirus (HPV) vaccination. The pentapeptid sharing between HPV's antigens, adrenergic receptors and muscarinic acetylcholine receptors supports this assumption. The dysregulating effects of the autoantibodies against calcium and potassium ion channels can be the basis for autoimmune phenocopies of genetic cardiac channelopathies, which are also associated with SCD.

摘要

心源性猝死 (SCD) 是指由于心脏原因导致的意外死亡,发生在已知或未知心脏疾病的患者中,时间较短(一般在症状出现后 1 小时内)。患有心肌病、心肌炎、缺血性心脏病和心脏通道病的患者有发生 SCD 的风险。然而,即使在进行了死后基因检测后,仍有一定比例的年轻(<35 岁)心源性猝死尸检阴性病例无法解释。针对心脏蛋白的自身抗体可能潜在地参与不同心脏疾病的发病机制,并导致无法解释的心源性猝死。在这篇综述中,我们分析了阐明这些自身抗体在不同心脏疾病患者中的流行程度及其病理生理相关性的临床和动物研究。我们提出了一种与心脏疾病相关的自身抗体的分类,并重点关注它们的分子和细胞作用。抗β肾上腺素能受体抗体和抗毒蕈碱乙酰胆碱受体抗体影响心肌电生理特性,并被报道为不同心脏疾病患者 SCD 的独立预测因子。针对 HPV 疫苗接种后心脏相关不良反应提出了自身免疫机制。HPV 抗原、肾上腺素能受体和毒蕈碱乙酰胆碱受体之间的五肽共享支持了这一假设。针对钙和钾离子通道的自身抗体的失调作用可能是遗传性心脏通道病自身免疫表型的基础,这也与 SCD 相关。

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