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Bitten by a bug or a bag? Transfusion-transmitted dengue: a rare complication in the bleeding surgical patient.被虫子咬了还是被袋子弄伤了?输血传播的登革热:出血性外科手术患者中的罕见并发症。
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Real-time symptomatic case of transfusion-transmitted dengue.输血传播登革热的实时症状病例。
Transfusion. 2015 May;55(5):961-4. doi: 10.1111/trf.12944. Epub 2015 Jan 21.
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Mosquito saliva serine protease enhances dissemination of dengue virus into the mammalian host.蚊子唾液丝氨酸蛋白酶可增强登革病毒在哺乳动物宿主体内的传播。
J Virol. 2014 Jan;88(1):164-75. doi: 10.1128/JVI.02235-13. Epub 2013 Oct 16.
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Aedes aegypti saliva contains a prominent 34-kDa protein that strongly enhances dengue virus replication in human keratinocytes.埃及伊蚊唾液中含有一种显著的34千道尔顿蛋白质,该蛋白质能强烈增强登革病毒在人类角质形成细胞中的复制。
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Dengue research opportunities in the Americas.美洲的登革热研究机会。
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6
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Transfusion. 2012 Aug;52(8):1667-71. doi: 10.1111/j.1537-2995.2012.03729.x. Epub 2012 Jun 7.
7
Dengue viremia in blood donors identified by RNA and detection of dengue transfusion transmission during the 2007 dengue outbreak in Puerto Rico.在 2007 年波多黎各登革热疫情期间,通过 RNA 鉴定献血者中的登革热病毒血症,并检测到登革热输血传播。
Transfusion. 2012 Aug;52(8):1657-66. doi: 10.1111/j.1537-2995.2012.03566.x. Epub 2012 Feb 17.
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Dynamics of dengue disease severity determined by the interplay between viral genetics and serotype-specific immunity.登革热疾病严重程度的动力学由病毒遗传学和血清型特异性免疫之间的相互作用决定。
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2012年巴西登革热疫情期间的输血传播登革热及相关临床症状

Transfusion-Transmitted Dengue and Associated Clinical Symptoms During the 2012 Epidemic in Brazil.

作者信息

Sabino Ester C, Loureiro Paula, Lopes Maria Esther, Capuani Ligia, McClure Christopher, Chowdhury Dhuly, Di-Lorenzo-Oliveira Claudia, Oliveira Lea C, Linnen Jeffrey M, Lee Tzong-Hae, Gonçalez Thelma, Brambilla Donald, Kleinman Steve, Busch Michael P, Custer Brian

机构信息

Departamento de Moléstias Infecciosas e Parasitárias, Instituto de Medicina Tropical, Universidade de São Paulo.

Faculdade de Ciências Médicas-UPE/Fundação Hemope, Recife.

出版信息

J Infect Dis. 2016 Mar 1;213(5):694-702. doi: 10.1093/infdis/jiv326. Epub 2015 Jun 8.

DOI:10.1093/infdis/jiv326
PMID:26908780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4747611/
Abstract

BACKGROUND

A linked donor-recipient study was conducted during epidemics in 2 cities in Brazil to investigate transfusion-transmitted (TT) dengue virus (DENV) by DENV RNA-positive donations.

METHODS

During February-June 2012, samples were collected from donors and recipients and retrospectively tested for DENV RNA by transcription-mediated amplification. Recipient chart review, using a case (DENV positive)-control (DENV negative and not known to be exposed) design, was conducted to assess symptoms.

RESULTS

Of 39 134 recruited blood donors, DENV-4 viremia was confirmed in 0.51% of donations from subjects in Rio de Janeiro and 0.80% of subjects in Recife. Overall, 42 DENV RNA-positive units were transfused into 35 recipients. Of these, 16 RNA-positive units transfused into 16 susceptible recipients were identified as informative: 5 cases were considered probable TT cases, 1 possible TT case, and 10 nontransmissions. The TT rate was 37.5% (95% confidence interval [CI], 15.2%-64.6%), significantly higher than the viremia rate of 0.93% (95% CI, .11%-3.34%) in nonexposed recipients (P < .0001). Chart review did not find significant differences between cases and controls in symptoms or mortality.

CONCLUSIONS

During a large epidemic of DENV-4 infection in Brazil, >0.5% of donations were RNA positive, and approximately one third of components resulted in TT. However, no significant clinical differences were evident between RNA-positive and RNA-negative recipients.

摘要

背景

在巴西两个城市的疫情期间开展了一项供受者关联研究,以调查登革病毒(DENV)RNA阳性献血导致的输血传播(TT)登革病毒情况。

方法

2012年2月至6月期间,从供者和受者中采集样本,并通过转录介导扩增对DENV RNA进行回顾性检测。采用病例(DENV阳性)-对照(DENV阴性且不知已暴露)设计对受者病历进行审查,以评估症状。

结果

在招募的39134名献血者中,里约热内卢受试者的献血中0.51%、累西腓受试者的献血中0.80%被确认为DENV-4病毒血症。总体而言,42个DENV RNA阳性单位被输注给35名受者。其中,输注给16名易感受者的16个RNA阳性单位被确定为有参考价值:5例被视为可能的TT病例,1例可能的TT病例,10例未发生传播。TT率为37.5%(95%置信区间[CI],15.2%-64.6%),显著高于未暴露受者中0.93%(95%CI,0.11%-3.34%)的病毒血症率(P<0.0001)。病历审查未发现病例与对照在症状或死亡率方面存在显著差异。

结论

在巴西DENV-4感染的大规模疫情期间,>0.5%的献血RNA呈阳性,约三分之一的成分导致了TT。然而,RNA阳性和RNA阴性受者之间没有明显的临床差异。