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川崎病的流行病学与发病机制

The Epidemiology and Pathogenesis of Kawasaki Disease.

作者信息

Rowley Anne H, Shulman Stanford T

机构信息

Department of Pediatrics, Northwestern University Feinberg School of Medicine, The Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, United States.

出版信息

Front Pediatr. 2018 Dec 11;6:374. doi: 10.3389/fped.2018.00374. eCollection 2018.

Abstract

Epidemiologic and clinical features of Kawasaki Disease (KD) strongly support an infectious etiology. KD is worldwide, most prominently in Japan, Korea, and Taiwan, reflecting increased genetic susceptibility among Asian populations. In Hawaii, KD rates are 20-fold higher in Japanese ethnics than in Caucasians, intermediate in other ethnicities. The age distribution of KD, highest in children < 2 yo, lower in those < 6 months, is compatible with infection by a ubiquitous agent resulting in increasing immunity with age and with transplacental immunity, as with some classic viruses. The primarily winter-spring KD seasonality and well-documented Japanese epidemics with wave-like spread also support an infectious trigger. We hypothesize KD pathogenesis involves an RNA virus that usually causes asymptomatic infection but KD in a subset of genetically predisposed children. CD8 T cells, oligoclonal IgA, and upregulation of cytotoxic T cell and interferon pathway genes in the coronaries in fatal KD also support a viral etiology. Cytoplasmic inclusion bodies in ciliated bronchial epithelium identified by monoclonal antibodies made from oligoclonal IgA heavy chains also supports a viral etiology. Recent availability of "second generation" antibodies from KD peripheral blood plasmablasts may identify a specific viral antigen. Thus, we propose an unidentified ("new") RNA virus infects bronchial epithelium usually causing asymptomatic infection but KD in a subset of genetically predisposed children. The agent persists in inclusion bodies, with intermittent respiratory shedding, entering the bloodstream via macrophages targeting coronaries. Antigen-specific IgA plasma cells and CD8 T cells respond but coronaries can be damaged. IVIG may include antibody against the agent. Post infection, 97-99% of KD patients are immune to the agent, protected against recurrence. The agent can spread either from those with asymptomatic primary infection in winter-spring or from a previously infected contact who intermittently sheds the agent.

摘要

川崎病(KD)的流行病学和临床特征有力地支持了其感染性病因。KD在全球范围内均有发生,在日本、韩国和台湾最为显著,这反映出亚洲人群中遗传易感性增加。在夏威夷,日裔儿童的KD发病率比白种人高20倍,其他种族则处于中间水平。KD的年龄分布在2岁以下儿童中最高,6个月以下儿童中较低,这与一种普遍存在的病原体感染相符,随着年龄增长免疫力增强以及存在经胎盘免疫,就像一些经典病毒一样。主要在冬春季节的KD季节性以及日本有充分记录的呈波浪状传播的疫情也支持存在感染触发因素。我们推测KD的发病机制涉及一种RNA病毒,该病毒通常引起无症状感染,但在一部分具有遗传易感性的儿童中会引发KD。致命性KD患者冠状动脉中CD8 T细胞、寡克隆IgA以及细胞毒性T细胞和干扰素途径基因的上调也支持病毒病因。用寡克隆IgA重链制备的单克隆抗体鉴定出的纤毛支气管上皮中的细胞质包涵体也支持病毒病因。最近从KD外周血浆母细胞获得的“第二代”抗体可能会识别出一种特定的病毒抗原。因此,我们提出一种未确定的(“新的”)RNA病毒感染支气管上皮,通常引起无症状感染,但在一部分具有遗传易感性的儿童中会引发KD。该病原体存在于包涵体中,通过间歇性呼吸道排出,经巨噬细胞进入血液循环并靶向冠状动脉。抗原特异性IgA浆细胞和CD8 T细胞会作出反应,但冠状动脉可能会受损。静脉注射免疫球蛋白(IVIG)可能包含针对该病原体的抗体。感染后,97 - 99%的KD患者对该病原体免疫,可防止复发。该病原体可从冬春季节无症状原发性感染的患者传播,或从先前感染且间歇性排出该病原体的接触者传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3de7/6298241/c2667dc0d524/fped-06-00374-g0001.jpg

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