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本文引用的文献

1
Susceptible and protective HLA class 1 alleles against dengue fever and dengue hemorrhagic fever patients in a Malaysian population.马来西亚人群中对登革热和登革出血热患者具有易感性和保护性的 HLA 1 类等位基因。
PLoS One. 2010 Sep 28;5(9):e13029. doi: 10.1371/journal.pone.0013029.
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Dengue virus pathogenesis: an integrated view.登革热病毒发病机制:综合观点。
Clin Microbiol Rev. 2009 Oct;22(4):564-81. doi: 10.1128/CMR.00035-09.
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Molecular evolution of dengue viruses: contributions of phylogenetics to understanding the history and epidemiology of the preeminent arboviral disease.登革病毒的分子进化:系统发育学对理解这种主要虫媒病毒疾病的历史和流行病学的贡献。
Infect Genet Evol. 2009 Jul;9(4):523-40. doi: 10.1016/j.meegid.2009.02.003. Epub 2009 Feb 13.
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Severe dengue epidemics in Sri Lanka, 2003-2006.2003 - 2006年斯里兰卡的严重登革热疫情
Emerg Infect Dis. 2009 Feb;15(2):192-9. doi: 10.3201/eid1502.080926.
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Understanding the contribution of cellular immunity to dengue disease pathogenesis.了解细胞免疫对登革热疾病发病机制的作用。
Immunol Rev. 2008 Oct;225:300-13. doi: 10.1111/j.1600-065X.2008.00678.x.
6
Protective and enhancing HLA alleles, HLA-DRB1*0901 and HLA-A*24, for severe forms of dengue virus infection, dengue hemorrhagic fever and dengue shock syndrome.保护性和增强性 HLA 等位基因 HLA-DRB1*0901 和 HLA-A*24 与登革热病毒感染的严重形式、登革出血热和登革休克综合征相关。
PLoS Negl Trop Dis. 2008 Oct 1;2(10):e304. doi: 10.1371/journal.pntd.0000304.
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Preservation of a critical epitope core region is associated with the high degree of flaviviral cross-reactivity exhibited by a dengue-specific CD4+ T cell clone.一个登革热特异性CD4 + T细胞克隆所表现出的高度黄病毒交叉反应性与一个关键表位核心区域的保存有关。
Eur J Immunol. 2008 Apr;38(4):1050-1057. doi: 10.1002/eji.200737699.
8
Varicella zoster virus glycoprotein E-specific CD4+ T cells show evidence of recent activation and effector differentiation, consistent with frequent exposure to replicative cycle antigens in healthy immune donors.水痘带状疱疹病毒糖蛋白E特异性CD4+ T细胞显示出近期活化和效应分化的证据,这与健康免疫供体频繁接触复制周期抗原一致。
Clin Exp Immunol. 2008 Jun;152(3):522-31. doi: 10.1111/j.1365-2249.2008.03633.x. Epub 2008 Mar 20.
9
High pro-inflammatory cytokine secretion and loss of high avidity cross-reactive cytotoxic T-cells during the course of secondary dengue virus infection.在二次登革病毒感染过程中促炎细胞因子的高分泌及高亲和力交叉反应性细胞毒性T细胞的丧失。
PLoS One. 2007 Dec 5;2(12):e1192. doi: 10.1371/journal.pone.0001192.
10
Dengue fever climbs the social ladder.登革热在社会阶层中蔓延。
Nature. 2007 Aug 16;448(7155):734-5. doi: 10.1038/448734a.

鉴定针对登革热病毒高度保守区域的血清型特异性 T 细胞反应。

Identification of serotype-specific T cell responses to highly conserved regions of the dengue viruses.

机构信息

Department of Microbiology, University of Sri Jayawardanapura, Nugegoda, Sri Lanka.

出版信息

Clin Exp Immunol. 2012 May;168(2):215-23. doi: 10.1111/j.1365-2249.2012.04566.x.

DOI:10.1111/j.1365-2249.2012.04566.x
PMID:22471283
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3390523/
Abstract

Determining previous infecting dengue virus (DENV) serotypes has been difficult due to highly cross-reactive immune responses from previous DENV infections. Determining the correlates of serotype-specific immune responses would be crucial in understanding dengue transmission in the community and would also help to determine the correlates of protective immune responses. Therefore, we set out to define highly conserved, serotype-specific regions of the DENVs. Serotype-specific and highly conserved regions of the four DENV serotypes were identified using Basic Local Alignment Search Tool (BLAST) searches and custom perl scripts. Using ex-vivo and cultured enzyme-linked immunospot (ELISPOT) assays, we identified serotype-specific T cell epitopes within the four DENV serotypes in healthy adult donors from Sri Lanka. We identified T cell responses to 19 regions of the four DENV serotypes. Six peptides were from the NS2A region and four peptides were from the NS4A region. All immune donors responded to peptides of at least two DENV serotypes, suggesting that heterologous infection is common in Sri Lanka. Eight of 20 individuals responded to at least two peptides of DENV-4, despite this serotype not being implicated previously in any of the epidemics in Sri Lanka. The use of these regions to determine past and current infecting DENV serotypes will be of value to characterize further the dynamics of silent dengue transmission in the community. In addition, these T cell responses to these regions could be used to characterize DENV serotype-specific immune responses and thus possibly help us to understand the immune correlates of a protective immune response.

摘要

由于先前感染的登革热病毒(DENV)引起的高度交叉反应性免疫反应,确定先前感染的登革热病毒(DENV)血清型一直很困难。确定血清型特异性免疫反应的相关性对于了解社区中的登革热传播至关重要,也有助于确定保护性免疫反应的相关性。因此,我们着手确定 DENV 的高度保守、血清型特异性区域。使用基本局部比对搜索工具(BLAST)搜索和自定义 perl 脚本,确定了四种 DENV 血清型的血清型特异性和高度保守区域。使用体外和培养酶联免疫斑点(ELISPOT)测定法,我们在来自斯里兰卡的健康成年供体中确定了四种 DENV 血清型内的血清型特异性 T 细胞表位。我们在四种 DENV 血清型中鉴定出了针对 19 个区域的 T 细胞反应。其中 6 个肽来自 NS2A 区,4 个肽来自 NS4A 区。所有免疫供体均对至少两种 DENV 血清型的肽产生反应,表明在斯里兰卡异源感染很常见。尽管之前在斯里兰卡的任何一次流行中都没有涉及到 DENV-4,但仍有 20 个人中有 8 个人对 DENV-4 的至少两个肽产生反应。这些区域的使用将有助于进一步确定社区中隐性登革热传播的动态,以确定过去和当前感染的 DENV 血清型。此外,这些对这些区域的 T 细胞反应可用于表征 DENV 血清型特异性免疫反应,从而可能有助于我们了解保护性免疫反应的免疫相关性。