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急性川崎病数月至数年后,在纤毛支气管上皮细胞中出现含RNA的胞质包涵体。

RNA-containing cytoplasmic inclusion bodies in ciliated bronchial epithelium months to years after acute Kawasaki disease.

作者信息

Rowley Anne H, Baker Susan C, Shulman Stanford T, Garcia Francesca L, Fox Linda M, Kos Ian M, Crawford Susan E, Russo Pierre A, Hammadeh Rashid, Takahashi Kei, Orenstein Jan M

机构信息

Department of Pediatrics, Northwestern University Feinberg School of Medicine, The Center for Kawasaki Disease, The Children's Memorial Hospital, Chicago, Illinois, USA.

出版信息

PLoS One. 2008 Feb 13;3(2):e1582. doi: 10.1371/journal.pone.0001582.

DOI:10.1371/journal.pone.0001582
PMID:18270572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2216059/
Abstract

BACKGROUND

Kawasaki Disease (KD) is the most common cause of acquired heart disease in children in developed nations. The KD etiologic agent is unknown but likely to be a ubiquitous microbe that usually causes asymptomatic childhood infection, resulting in KD only in genetically susceptible individuals. KD synthetic antibodies made from prevalent IgA gene sequences in KD arterial tissue detect intracytoplasmic inclusion bodies (ICI) resembling viral ICI in acute KD but not control infant ciliated bronchial epithelium. The prevalence of ICI in late-stage KD fatalities and in older individuals with non-KD illness should be low, unless persistent infection is common.

METHODS AND PRINCIPAL FINDINGS

Lung tissue from late-stage KD fatalities and non-infant controls was examined by light microscopy for the presence of ICI. Nucleic acid stains and transmission electron microscopy (TEM) were performed on tissues that were strongly positive for ICI. ICI were present in ciliated bronchial epithelium in 6/7 (86%) late-stage KD fatalities and 7/27 (26%) controls ages 9-84 years (p = 0.01). Nucleic acid stains revealed RNA but not DNA within the ICI. ICI were also identified in lung macrophages in some KD cases. TEM of bronchial epithelium and macrophages from KD cases revealed finely granular homogeneous ICI.

SIGNIFICANCE

These findings are consistent with a previously unidentified, ubiquitous RNA virus that forms ICI and can result in persistent infection in bronchial epithelium and macrophages as the etiologic agent of KD.

摘要

背景

川崎病(KD)是发达国家儿童后天性心脏病的最常见病因。KD的病原体尚不清楚,但可能是一种普遍存在的微生物,通常引起无症状的儿童期感染,仅在基因易感性个体中导致KD。由KD动脉组织中普遍存在的IgA基因序列制成的KD合成抗体在急性KD中可检测到类似于病毒胞质内包涵体(ICI)的结构,但在对照婴儿的纤毛支气管上皮中则检测不到。除非持续感染很常见,否则ICI在晚期KD死亡病例和非KD疾病的老年个体中的患病率应该较低。

方法和主要发现

通过光学显微镜检查晚期KD死亡病例和非婴儿对照的肺组织中是否存在ICI。对ICI呈强阳性的组织进行核酸染色和透射电子显微镜(TEM)检查。在6/7(86%)的晚期KD死亡病例的纤毛支气管上皮中以及7/27(26%)年龄在9 - 84岁的对照者中发现了ICI(p = 0.01)。核酸染色显示ICI内有RNA但无DNA。在一些KD病例的肺巨噬细胞中也发现了ICI。对KD病例的支气管上皮和巨噬细胞进行TEM检查发现了细颗粒状均匀的ICI。

意义

这些发现与一种先前未被识别的、普遍存在的RNA病毒一致,该病毒形成ICI,并可在支气管上皮和巨噬细胞中导致持续感染,是KD的病原体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4490/2216059/c7d300f7905f/pone.0001582.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4490/2216059/447b5d4b5c69/pone.0001582.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4490/2216059/46d5048f3fae/pone.0001582.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4490/2216059/297f1093b1fe/pone.0001582.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4490/2216059/9aeb89f550d8/pone.0001582.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4490/2216059/c7d300f7905f/pone.0001582.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4490/2216059/447b5d4b5c69/pone.0001582.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4490/2216059/46d5048f3fae/pone.0001582.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4490/2216059/297f1093b1fe/pone.0001582.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4490/2216059/9aeb89f550d8/pone.0001582.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4490/2216059/c7d300f7905f/pone.0001582.g005.jpg

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