Kawasaki Disease, Multisystem Inflammatory Syndrome in Children: Antibody-Induced Mast Cell Activation Hypothesis

D. Ricke, Nicole Gherlone, Philip Fremont-Smith, P. Tisdall, M. Fremont-Smith
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引用次数: 8

Abstract

Multisystem Inflammatory Syndrome in Children (MIS-C) is appearing in infants, children, and young adults in association with COVID-19 (coronavirus disease 2019) infections of SARS-CoV-2. Kawasaki Disease (KD) is one of the most common vasculitides of childhood. KD presents with similar symptoms to MIS-C especially in severe forms such as Kawasaki Disease Shock Syndrome (KDSS). The observed symptoms for MIS-C and KD are consistent with Mast Cell Activation Syndrome (MCAS) characterized by inflammatory molecules released from activated mast cells. Based on the associations of KD with multiple viral and bacterial pathogens, we put forward the hypothesis that KD and MIS-C result from antibody activation of mast cells by Fc receptorbound pathogen antibodies causing a hyperinflammatory response upon second pathogen exposure. Within this hypothesis, MIS-C may be atypical KD or a KD-like disease associated with SARS-CoV-2. We extend the mast cell hypothesis that increased histamine levels are inducing contraction of effector cells with impeded blood flow through cardiac capillaries. In some patients, pressure from impeded blood flow, within cardiac capillaries, may result in increased coronary artery blood pressure leading to aneurysms, a well-known complication in KD.
川崎病,儿童多系统炎症综合征:抗体诱导肥大细胞活化假说
儿童多系统炎症综合征(MIS-C)出现在婴儿、儿童和年轻人中,与COVID-19(冠状病毒病2019)感染SARS-CoV-2有关。川崎病是儿童最常见的血管病之一。KD表现出与misc相似的症状,特别是在严重的形式,如川崎病休克综合征(KDSS)。观察到的MIS-C和KD的症状与肥大细胞活化综合征(MCAS)一致,其特征是活化肥大细胞释放炎症分子。基于KD与多种病毒和细菌病原体的关联,我们提出了KD和MIS-C是由Fc受体结合的病原体抗体激活肥大细胞导致第二次病原体暴露时的高炎症反应引起的假设。在这一假设中,misc可能是与SARS-CoV-2相关的非典型KD或KD样疾病。我们扩展肥大细胞假说,即增加的组胺水平诱导效应细胞收缩,阻碍血液通过心脏毛细血管。在一些患者中,心脏毛细血管内血流受阻的压力可能导致冠状动脉血压升高,导致动脉瘤,这是众所周知的KD并发症。
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