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Kansenshogaku zasshi. The Journal of the Japanese Association for Infectious Diseases最新文献

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Results of a Questionnaire Survey on the Genetic Testing for Infectious Diseases 传染病基因检测问卷调查结果
Pub Date : 2018-05-20 DOI: 10.11150/kansenshogakuzasshi.92.331
K. Yanagihara, N. Kaku, Hiromichi Suzuki, H. Niimi, H. Mikamo, Tetsuya Matsumoto, K. Tateda
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引用次数: 0
[Hepatitis A]. 甲型肝炎。
Pub Date : 2018-05-01 DOI: 10.1542/9781610021470-part03-hepatitis_a
Y. Moritsugu
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引用次数: 0
A Case of Mycotic Aneurysm of the Abdominal Aorta Caused by Aspergillus fumigatus in a Tsunami Survivor After the East Japan Great Earthquake 东日本大地震后海啸幸存者一例由烟曲霉引起的腹主动脉真菌性动脉瘤
Pub Date : 2018-03-20 DOI: 10.11150/kansenshogakuzasshi.92.138
Y. Fujikawa, Yoshiaki Gu, Kengo Oshima, Misa Sogi, Chihiro Oe, Noriomi Ishibashi, Hiroaki Baba, S. Inomata, Makiko Yoshida, S. Endo, M. Kaku
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引用次数: 0
Causative Bacteria and Proper Antibiotics Selection:a Prospective Investigation of 101 Patients with Cellulitis 101例蜂窝织炎病原菌及抗生素选择的前瞻性调查
Pub Date : 2018-03-20 DOI: 10.11150/kansenshogakuzasshi.92.115
Y. Moriyama, K. Iwamoto, M. Katagiri, Reiko Kessoku
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引用次数: 0
Evaluation of Performance Among Norovirus Antigen Detection Kits with Immunochromatography 免疫层析法检测诺如病毒抗原试剂盒的性能评价
Pub Date : 2018-03-20 DOI: 10.11150/kansenshogakuzasshi.92.120
Yuki Sato, M. Shinagawa, Yusuke Takahashi, Masachika Saeki, Yuki Yakuwa, S. Takahashi
We have evaluated the performance among four brands of immunochromatography (IC) assay kits, available in the market in Japan, for detection of norovirus antigen and compared with Real Time PCR (RT-PCR) assays. The four brands used were ImmunoCatch-Noro (A Kit, EIKEN CHEMICAL Co., Ltd., Japan), Quick Chaser-Noro (B Kit, MIZUHO MEDY Co., Ltd., Saga, Japan), GE test Noro Nissui (C Kit, NISSUI PHARMACEUTICAL Co., Ltd., Tokyo, Japan), and Quick Navi-Noro2 (D Kit, DENKA SEIKEN Co., Ltd., Tokyo, Japan). The results from the RT-PCR analysis of 69 suspected cases of norovirus infection identified 6 cases of Genogroup I (GI) and 22 cases of Genogroup II (GII) infection, whereas one case among them had a mixed infection of both GI and GII. The virus titers of the positive samples varied from 1.54×10 1 to 3.14× 10 8 copies/ μ L. The genotypes identified were as follows:GI, GI.1 (1 case each), GI.2 (3 cases), and GI.3 (2 cases);GII, GII.2 (1 case each), GII.4 (7 cases), GII.13 (2 cases), and GII.17 (12 cases). The positive concordance rates between the IC assay kits and the Real Time RT-PCR were as follows:A, 59.3 % ;B, 51.9 % ;C, 51.9 % ;and
我们评估了日本市场上四种品牌的免疫层析(IC)检测试剂盒检测诺如病毒抗原的性能,并与实时PCR (RT-PCR)检测方法进行了比较。使用的四个品牌分别是immunocapture -Noro (A试剂盒,EIKEN CHEMICAL Co., Ltd.,日本)、Quick Chaser-Noro (B试剂盒,MIZUHO medicine Co., Ltd., Saga,日本)、GE test Noro Nissui (C试剂盒,Nissui PHARMACEUTICAL Co., Ltd.,日本东京)和Quick Navi-Noro2 (D试剂盒,DENKA SEIKEN Co., Ltd.,日本东京)。对69例诺如病毒疑似感染病例进行RT-PCR分析,鉴定为基因I型(GI)感染6例,基因II型(GII)感染22例,其中1例为GI和GII混合感染。阳性标本的病毒滴度为1.54×10 1 ~ 3.14× 10 8拷贝/ μ l,鉴定的基因型为GI、GI.1(各1例)、GI.2(3例)和GI.3(2例);GII、GII.2(各1例)、GII.4(7例)、GII.13(2例)和GII.17(12例)。IC试剂盒与Real Time RT-PCR的阳性符合率分别为:A, 59.3%;B, 51.9%;C, 51.9%
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引用次数: 0
Efficacy, Safety and Immunogenicity of a Novel Adjuvanted Subunit Herpes Zoster Vaccine in Japanese Aged 50 Years and 70 Years and Older 一种新型佐剂带状疱疹亚单位疫苗在日本50岁和70岁及以上人群中的有效性、安全性和免疫原性
Pub Date : 2018-03-20 DOI: 10.11150/kansenshogakuzasshi.92.103
H. Ikematsu, Nobuyuki Yamashita, M. Ogawa, Motonori Hirano, Martina Kovac, D. Watanabe
Two large randomized multinational efficacy trials (ZOE-50 and ZOE-70) showed that the novel herpes zoster subunit vaccine (HZ/su) candidate containing varicella-zoster virus glycoprotein E (gE) and the AS01 B adjuvant system reduced the risk of herpes zoster (HZ) and post-herpetic neuralgia (PHN) by more than 90%. We conducted a descriptive subgroup analysis in subjects enrolled in Japan in these studies and evalu-ated the results.
两项大型随机多国疗效试验(ZOE-50和ZOE-70)显示,含有水痘-带状疱疹病毒糖蛋白E (gE)和AS01 B佐剂系统的新型带状疱疹亚单位疫苗(HZ/su)候选疫苗可将带状疱疹(HZ)和疱疹后神经痛(PHN)的风险降低90%以上。我们对在日本参加这些研究的受试者进行了描述性亚组分析,并评估了结果。
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引用次数: 3
Evaluation of a Newly Developed Immunochromatographic Assay, for the Detection of HBsAg with Sensitivity and Specificity Equivalent to Those of Chemiluminescent Immunoassays 评价一种新开发的免疫层析法检测HBsAg,其灵敏度和特异性与化学发光免疫法相当
Pub Date : 2018-03-20 DOI: 10.11150/kansenshogakuzasshi.92.126
I. Nakagiri, H. Wada, H. Tokunaga, T. Tasaka, T. Sugihara
We evaluated a new immunochromatographic assay (ICA) for the detection of hepatitis B surface antigen (HBsAg) (Alere HBsAg;Alere Medical Co., Ltd) using 275 serum and 40 whole blood (EDTA) samples screened in our hospital. Five seroconversion panels and a reference panel according to the WHO International Standard for HBsAg were also tested. The performance of the ICA was compared with that of the conventional ICA (ICA2), chemiluminescent enzyme immunoassay (qualitative CLEIA), and chemiluminescent assay (quantitative CLIA). The sensitivity of the ICA in 54 HBV DNA positive specimens with a RT-PCR (TaqMan assay) was 98.1% (53/54), better than the ICA2 -92.6%- (50/54) and the CLEIA -96.3%- (52/54), and equivalent to the CLIA -98.1%- (53/54). The specificity in 221 HBV DNA negative specimens was 100%, better than the ICA2 -99.5%- (220/221), and equivalent to the CLEIA and CLIA. The ICA indicated a de-tectability superior to the ICA2 and CLEIA, and equivalent to the CLIA in the seroconversion panels. The limit of detection of the assay was calculated as 0.1IU/mL based on the results of the CLIA assay with the seroconversion panels. This assay using an avidin-biotin format demonstrated to show an excellent sensitivity and specificity in the clinical specimens and the panels. We conclude that this simple and rapid assay with a capability for whole blood sample application is suitable and applicable for use in risk management in patients with resolved HBV infection as well as in emergency and resource-limited settings.
我们利用在我院筛选的275份血清和40份全血(EDTA)样本,评估了一种新的检测乙型肝炎表面抗原(HBsAg)的免疫层析法(ICA) (Alere HBsAg;Alere Medical Co., Ltd)。根据世卫组织乙肝表面抗原国际标准,还检测了5个血清转换组和一个参考组。将其与常规ICA (ICA2)、化学发光酶免疫分析法(定性CLEIA)和化学发光法(定量CLIA)的性能进行比较。采用RT-PCR (TaqMan法)检测54例HBV DNA阳性标本,ICA的敏感性为98.1%(53/54),优于ICA2 -92.6%-(50/54)和CLEIA -96.3%-(52/54),与CLIA -98.1%-(53/54)相当。221例HBV DNA阴性标本特异性为100%,优于ICA2 -99.5%-(220/221),与CLEIA和CLIA相当。ICA的可检测性优于ICA2和CLEIA,在血清转换面板上与CLIA相当。根据使用血清转换板的CLIA测定结果计算出该方法的检出限为0.1IU/mL。该试验采用亲和素-生物素格式,在临床标本和面板中显示出极好的敏感性和特异性。我们的结论是,这种具有全血样本应用能力的简单快速检测方法适合并适用于解决HBV感染的患者的风险管理以及急诊和资源有限的环境。
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引用次数: 0
A Case of Helicobacter cinaedi Isolated from Inflammatory Intestinal Mucosa Following Bacteremia with Diffuse Large B-cell Lymphoma 细菌血症合并弥漫性大b细胞淋巴瘤后炎性肠黏膜分离出中国幽门螺杆菌1例
Pub Date : 2018-03-20 DOI: 10.11150/kansenshogakuzasshi.92.133
Hisaaki Nishio, Kohsuke Asagoe
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引用次数: 0
非流行地(北海道)で経験したレプトスピラ症の1例 在非疫区(北海道)经历的钩端螺旋体症的1例
Pub Date : 2018-03-20 DOI: 10.11150/KANSENSHOGAKUZASSHI.92.144
卓 小笠原, 岡部 敏明, 成田 光生, 大島 美保, 村田 亮
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引用次数: 1
Safety and Prophylactic Efficacy Against Influenza of Laninamivir Octanoate Hydrate,A Long-acting Neuraminidase Inhibitor, in High-risk Patients Including the Elderly 长效神经氨酸酶抑制剂水合辛酸兰尼米韦在包括老年人在内的高危患者中的安全性和预防流感的有效性
Pub Date : 2018-01-20 DOI: 10.11150/kansenshogakuzasshi.92.51
A. Watanabe, S. Kashiwagi, H. Ikematsu, H. Yamaguchi, S. Seki, Kazuhito Shiosakai
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引用次数: 0
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Kansenshogaku zasshi. The Journal of the Japanese Association for Infectious Diseases
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