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Renal And Neurological Outcomes In Chronically Infected West Nile Virus Patients

Renal And Neurological Outcomes In Chronically Infected West Nile Virus Patients
慢性感染西尼罗病毒患者的肾脏和神经系统结果
批准号:
8700313
负责人:
KRISTY MURRAY
金额:
$37.65万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-08-16 至 2016-07-31

项目摘要

项目成果

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中文摘要
翻译
描述(由申请方提供):西尼罗河病毒(WNV)是一种重要的新出现的黄病毒,可导致人类急性,有时甚至致命的脑炎。在动物模型中,西尼罗河病毒可以持续感染中枢神经系统(CNS)和肾脏。当我们发现我们队列中的WNV患者数量超过预期时,我们开始担心人类可能会发生类似的持续感染,这些患者正在经历进行性神经系统疾病和肾衰竭。申请人有一个大的,有充分记录的队列112名西尼罗河病毒患者,她从2002年开始跟踪。我们发现,77%的脑炎患者有异常的神经系统检查,包括63%的人有受损的串联步态,提示前庭-小脑和/或背柱功能障碍。此外,23%的患者发生肾脏疾病,其中5例死于肾衰竭。我们的初步研究发现症状持续存在,持续可检测的IgM抗体反应和细胞因子表达改变之间存在关联,这加强了我们的假设,即一些患者可能存在持续感染。最近,我们报告了25名队列参与者中的5名(20%)尿液含有WNV病毒RNA,这是人类持续感染WNV的首次记录证据。其中两人患有肾衰竭。队列的进一步测试显示,共有21/55(38%)例患者在尿液中脱落WNV RNA;其中45%的患者报告在急性感染后发生肾脏疾病。我们的发现是非常新颖和令人担忧的,考虑到美国各地超过25,000名WNV患者已报告给CDC。我们迫切需要进一步研究这些大体终点的病理学病变和定义WNV持续感染的临床参数,这是本提案的目标。因此,拟议研究的目的是确定与WNV持续感染相关的肾脏和神经病理学和结局。我们计划确定肾功能衰竭的程度和尿中病毒脱落的模式,通过肾活检组织病理学检查、病毒分离株的基因型和表型分析确定感染细胞类型,以确定与肾嗜性潜在相关的突变,并进行神经认知检查、体积MRI和电生理研究,以确定CNS中病理性病变的位置。该建议的假设是,持续感染与严重和进行性肾脏和神经病理学相关。这项研究将提供必要的信息,以评估患者的持续感染和制定治疗方案。
英文摘要
DESCRIPTION (provided by applicant): West Nile virus (WNV) is an important emerging flavivirus resulting in acute and sometimes fatal encephalitis in humans. In animal models, WNV can persistently infect the central nervous system (CNS) and the kidneys. We became concerned that a similar persistent infection could occur in humans when we discovered a larger than expected number of WNV patients in our cohort were experiencing progressive neurologic disease and kidney failure. The applicant has a large, well-documented cohort of 112 WNV patients who she has followed since 2002. We have found that 77% of patients who presented with encephalitis have abnormal neurologic exams, including 63% who have impaired tandem gait, suggestive of vestibular-cerebellar and/or dorsal column dysfunction. Additionally, 23% of patients developed renal disease, including 5 who died from renal failure. Our preliminary research found associations between persistence of symptoms, sustained detectable IgM antibody response, and altered cytokine expressions, which strengthened our hypothesis that some patients might have persistent infection. Recently, we reported 5 out of 25 (20%) cohort participants' urine contained WNV viral RNA, which is the first ever documented evidence of persistent WNV infection in humans. Two of these individuals are in renal failure. Further testing of the cohort has revealed a total of 21/55 (38%) patients shedding WNV RNA in the urine; 45% of these patients reported developing kidney disease after their acute infection. Our findings are very novel and worrisome considering more than 25,000 WNV patients across the US have been reported to CDC. We urgently need to further investigate the pathologic lesions underlying these gross endpoints and the clinical parameters that define persistent infection with WNV, which is the goal of this proposal. Thus, the objective of the proposed study is to determine the renal and neurological pathology and outcomes associated with persistent infection with WNV. We plan to identify the degree of renal failure and pattern of shedding of virus in the urine, identify the infected cell types through histopathologic examination of renal biopsies, genotypic and phenotypic analysis of virus isolates to determine mutations potentially related to renal tropism, and perform neurocognitive examinations, volumetric MRI, and electrophysiological studies to determine the location of pathologic lesions in the CNS. It is the hypothesis of this proposal that persistent infection is associated with severe and progressive renal and neurological pathology. This research will provide the information necessary to evaluate patients for persistent infection and develop treatment protocols.
期刊论文(12)
专著(0)
科研奖励(0)
会议论文
DOI: 10.3201/eid2209.152050
发表时间: 2016-09
期刊: Emerging infectious diseases
影响因子: 11.8
作者: [Vanichanan J, Salazar L, Wootton SH, Aguilera E, Garcia MN, Murray KO, Hasbun R]
通讯作者: Hasbun R
Proximity of residence to bodies of water and risk for west nile virus infection: a case-control study in Houston, Texas.
居住地靠近水体和西尼罗河病毒感染的风险:德克萨斯州休斯顿的一项病例对照研究。
DOI: 10.1155/2012/159578
发表时间: 2012
期刊: Journal of biomedicine & biotechnology
影响因子: --
作者: [Nolan,MelissaS, Zangeneh,Ana, Khuwaja,SalmaA, Martinez,Diana, Rossmann,SusanN, Cardenas,Victor, Murray,KristyO]
通讯作者: Murray,KristyO
Does intra-individual neurocognitive variability relate to neuroinvasive disease and quality of life in West Nile Virus?
个体内神经认知变异与西尼罗河病毒的神经侵袭性疾病和生活质量有关吗?
DOI: 10.1007/s13365-018-0641-5
发表时间: 2018
期刊: Journal of neurovirology
影响因子: 3.2
作者: [Sheppard,DavidP, Woods,StevenPaul, Hasbun,Rodrigo, Salazar,Lucrecia, Nolan,MelissaS, Murray,KristyO]
通讯作者: Murray,KristyO
DOI: 10.3201/eid2301.161394
发表时间: 2017-01
期刊: Emerging infectious diseases
影响因子: 11.8
作者: [Murray KO, Gorchakov R, Carlson AR, Berry R, Lai L, Natrajan M, Garcia MN, Correa A, Patel SM, Aagaard K, Mulligan MJ]
通讯作者: Mulligan MJ
An Integrated One Health Approach to Detect and Respond to Emerging Disease Threats in High-Risk Regions of Central America
  • 批准号:
    10462456
  • 项目类别:
  • 资助金额:
    $39.41万
  • 财政年份:
    2018
  • 负责人:
    KRISTY MURRAY
  • 依托单位:
An Integrated One Health Approach to Detect and Respond to Emerging Disease Threats in High-Risk Regions of Central America
  • 批准号:
    10228537
  • 项目类别:
  • 资助金额:
    $90.83万
  • 财政年份:
    2018
  • 负责人:
    KRISTY MURRAY
  • 依托单位:
An Integrated One Health Approach to Detect and Respond to Emerging Disease Threats in High-Risk Regions of Central America
  • 批准号:
    10242607
  • 项目类别:
  • 资助金额:
    $25.0万
  • 财政年份:
    2018
  • 负责人:
    KRISTY MURRAY
  • 依托单位:
An Integrated One Health Approach to Detect and Respond to Emerging Disease Threats in High-Risk Regions of Central America
  • 批准号:
    10630167
  • 项目类别:
  • 资助金额:
    $44.5万
  • 财政年份:
    2018
  • 负责人:
    KRISTY MURRAY
  • 依托单位:
海外基金