New approach for the elucidation of the etiology of Kawasaki disease
New approach for the elucidation of the etiology of Kawasaki disease
批准号:
22591190
负责人:
SUZUKI Hiroyuki
金额:
$2.75万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2010
资助国家:
日本
项目状态:
已结题
起止时间:
2010 至 2012
中文摘要
我们收集了58例符合川崎病诊断标准并在我院住院的患者的咽拭子样本。将咽拭子细菌置于脑-心输注液体培养液中培养。使用DNA Mini Kit (QIAGEN)试剂盒提取细菌总DNA。以细菌总DNA为模板,对5个SAg基因-链球菌热原外毒素a型(SPE-A)、SPE-C、SPE-G、SPE-J和中毒性休克综合征毒素-1 (TSST -1)进行聚合酶链反应(PCR)。58例患者中检测到SPE-G基因7例,检测到SPE-J基因6例。58例患者中有1例同时检测到SPE-G和SPE-J基因。因此,在58例患者的12例(20.7%)咽拭子样本中检测到来自A群链球菌(GAS)的超抗原基因片段。这些结果是重复的,非常重要。然而,在所有检测到SPE-G和SPE-J基因的患者中均未检测到GAS。因此,任何一种细菌都具有这些超抗原基因是本研究的重点和主题。不幸的是,我们无法在这项研究中分离出细菌。
英文摘要
We collected the samples of throat swab from 58 patients who met the diagnostic criteria for Kawasaki disease and were admitted to our hospitals. Bacteria from throat swab were cultured in liquid culture solution (Brain-Heart-Infusion). W e extracted total DNA from those bacteria using DNA Mini Kit (QIAGEN). Using total DNA extracted from bacteria as a template, polymerase chain reaction (PCR) was performed for 5 SAg genes-streptococcal pyrogenic exotoxin type A(SPE-A), SPE-C, SPE-G, SPE-J, and toxic shock syndrome toxin-1 (TSST -1). SPE-G gene and SPE-J gene were detected in 7 and 6 of 58 patients, respectively. Both SPE-G gene and SPE-J gene were detected in one of 58 patients. Thus, gene fragments of superantigens derived from group A streptococcus (GAS) were detected in the samples of throat swabs from 12 of 58 patients (20.7%). These results were reproducted and very important. However, GAS was not detected from any patients in whom SPE-G and SPE-J gene were detected. Thus, it is very important point and the theme in this study that any kind of bacteria have these superantigen genes. Unfortunately, we could not isolate the bacteria in this study.
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IVIG 不応川崎病症例に対する CsA 療法時の血中カリウム濃度の検討
IVIG难治性川崎病患者 CsA 治疗期间血钾浓度的检测
DOI:
--
发表时间:
2012
期刊:
Prog Med
影响因子:
--
作者:
[垣本信幸, 鈴木啓之, 末永智浩, 武内 崇, 吉川徳茂, 渋田昌一, 濱田洋通, 本田隆文, 寺井 勝, 笹子久美子, 尾内善広, 鈴木洋一, 羽田 明]
通讯作者:
羽田 明
シクロスポリン A の難治性川崎病治療における現状と今後の展望
环孢素A治疗难治性川崎病的现状及展望
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[小西行彦, 他, 金子 一成, 鈴木啓之]
通讯作者:
鈴木啓之
川崎病は溶連菌毒素を中心とするスーパー抗原病? ランチョンセミナー:「川崎病の病因解明の最前線」
川崎病是一种以链球菌毒素为中心的超抗原疾病吗?午宴研讨会:《阐明川崎病发病机制的最前沿》
DOI:
--
发表时间:
2010
期刊:
影响因子:
--
作者:
[Ogawa T, Kuwagata M, 他5名, 鈴木啓之]
通讯作者:
鈴木啓之
2000年以降に和歌山県で発症した川崎病の臨床疫学像と悉皆的調査に基づく罹患率
2000年以后和歌山县川崎病临床流行病学及发病率综合调查
DOI:
--
发表时间:
2010
期刊:
影响因子:
--
作者:
[Onodera M, Nakamura M, Tanaka F, Takahashi T, Makita S, Ishisone T, Ishibashi Y, Itai K, Onoda T, Ohsawa M, Tanno K, Sakata K, Omama S, Ogasawara K, Ogawa A, Kuribayashi T, Sakamaki K, Okayama A., 北野尚美,鈴木啓之,武内 崇,末永智浩,渋田昌一,南 孝臣,上村 茂,竹下達也]
通讯作者:
北野尚美,鈴木啓之,武内 崇,末永智浩,渋田昌一,南 孝臣,上村 茂,竹下達也
IVIG 不応の川崎病症例に対するシクロスポリン A 療法
环孢素 A 治疗 IVIG 难治性川崎病病例
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[Yamaoka S, Ogihara T, Yasui M, Hasegawa M, Hira S, Oue S, Ubukata K, Watanabe H, Takahashi T, 亀井良政, 田中 英高., 鈴木啓之]
通讯作者:
鈴木啓之
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Functional analysis and identification of substrate proteins of mitochondrial sirtuins.
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System Stabilities and Anti-Fire Redundancy of Steel Frames in Fire
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