An antigen-detection assay to diagnose Babesia microti infection
诊断田鼠巴贝斯虫感染的抗原检测方法
基本信息
- 批准号:10200003
- 负责人:
- 金额:$ 69.21万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2018
- 资助国家:美国
- 起止时间:2018-01-10 至 2023-05-31
- 项目状态:已结题
- 来源:
- 关键词:Acute respiratory failureAmericanAnaplasmosisAnimalsAntibioticsAntibodiesAntigensBabesiaBabesia microtiBabesiosisBiologicalBiological AssayBlack-legged TickBloodBlood TransfusionBlood donorBlood specimenBorrelia microtiCenters for Disease Control and Prevention (U.S.)CharacteristicsClinicalClinical SensitivityComplexCongestive Heart FailureDNADevelopmentDiagnosisDiagnostic ProcedureDiffuseDiseaseDisease modelElderlyEnzyme-Linked Immunosorbent AssayEpitopesErythrocytesEvaluationGoalsGoldHealthHumanImmunocompetentImmunocompromised HostImmunofluorescence ImmunologicIndividualIndustry StandardInfectionInstitute of Medicine (U.S.)Kidney FailureLaboratoriesLeadLongitudinal prospective studyLyme DiseaseMalariaMethodsMicroscopicMicroscopyMonitorMonoclonal AntibodiesMusParasitemiaParasitesPatientsPerformancePhasePopulationProspective StudiesProteinsRNARecombinant ProteinsRecurrent diseaseRed CrossRelapseReportingResolutionRetrospective StudiesRiskSamplingSensitivity and SpecificitySerologySerumSigns and SymptomsSpecificityStatistical Data InterpretationSymptomsTechniquesTicksTransfusionTreatment FailureUnited StatesVascular blood supplyactive methodantibody detectionantigen detectionassay developmentbasecohortcostdesigndetection assaydiagnostic assayexperimental studyflugranulocytehuman diseasehuman modelimmunosuppressedinfection riskmortalitymouse modelpathogenrapid testtick transmissionvector tick
项目摘要
PROJECT SUMMARY
Human babesiosis is a malaria-like multisystem disease caused primarily by Babesia microti, an emerging
apicomplexan parasite that infects and develops within human erythrocytes. The parasite is transmitted to
humans by the tick vector Ixodes scapularis and can also be introduced through blood transfusion. Infection
can cause flu-like symptoms, and severe infection can be fatal, in particular in the immunosuppressed and the
elderly. Current methods for babesiosis diagnosis include microscopy, PCR, IFA and ELISA-based methods
that detect antibodies in serum from patients or donors. Each of these methods has major limitations, such as
insufficient sensitivity, high complexity, and low throughput. In addition, results from many of these assays
remain positive for months or years after resolution of active infection.
In Phase I of this project, we have developed a capture ELISA assay that can detect a protein of the parasite,
BmGPI12/BmSAI. We have identified pairs of monoclonal antibodies that can be used to capture BmGPI12 in
mouse and human samples. Our preliminary results demonstrate that this assay has an excellent sensitivity.
Using samples collected from infected mice, a well-established model of human disease, we demonstrated that
following successful treatment, our assay gives negative results while PCR and serology remain positive.
Thus, our assay may be useful in distinguishing active infection from past exposure.
In Phase II of this project, we will further develop this assay with the goal of applying for FDA clearance. We
will analyze several hundred animal and human samples to establish important characteristics of the assay
including sensitivity and specificity. These Phase II experiments are designed to give us a full understanding
of the potential biological indications and commercial usefulness of the assay.
项目摘要
人类巴贝斯虫病是一种类似疟疾的多系统疾病,主要由小巴贝斯虫引起,
在人体红细胞内感染和发育的顶复体寄生虫。寄生虫会传播到
人类通过蜱媒介肩胛硬蜱传播,也可以通过输血传播。感染
可引起流感样症状,严重感染可致命,特别是在免疫抑制和
老人目前诊断巴贝虫病的方法包括显微镜检查法、PCR法、IFA法和ELISA法
检测病人或捐赠者血清中的抗体这些方法都有很大的局限性,例如
灵敏度不足、复杂性高和吞吐量低。此外,许多这些测定的结果
活动性感染消退后数月或数年内仍保持阳性。
在该项目的第一阶段,我们开发了一种捕获ELISA测定法,可以检测寄生虫的蛋白质,
BmGPI12/BmSAI。我们已经鉴定了可用于捕获BmGPI 12的单克隆抗体对,
小鼠和人类样品。我们的初步结果表明,这种方法具有良好的灵敏度。
使用从受感染小鼠(一种已建立的人类疾病模型)收集的样本,我们证明,
成功治疗后,我们的检测结果为阴性,而PCR和血清学检测结果仍为阳性。
因此,我们的检测方法可能有助于区分活动性感染和既往感染。
在该项目的第二阶段,我们将进一步开发该检测试剂盒,目标是申请FDA批准。我们
将分析数百个动物和人类样本,以确定检测的重要特征
包括灵敏度和特异性。这些第二阶段的实验旨在让我们充分了解
潜在的生物学适应症和商业实用性的测定。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Michel Ledizet其他文献
Michel Ledizet的其他文献
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{{ truncateString('Michel Ledizet', 18)}}的其他基金
Vaccination against Zika virus infection using mosquito NeSt1 protein
使用蚊子 NeSt1 蛋白预防寨卡病毒感染的疫苗
- 批准号:
10194371 - 财政年份:2020
- 资助金额:
$ 69.21万 - 项目类别:
Vaccination against Zika virus infection using mosquito NeSt1 protein
使用蚊子 NeSt1 蛋白预防寨卡病毒感染的疫苗
- 批准号:
10081573 - 财政年份:2020
- 资助金额:
$ 69.21万 - 项目类别:
An antigen-detection assay to diagnose Babesia microti infection
诊断田鼠巴贝斯虫感染的抗原检测方法
- 批准号:
10403621 - 财政年份:2018
- 资助金额:
$ 69.21万 - 项目类别:
An antigen-detection assay to diagnose Babesia microti infection
诊断田鼠巴贝斯虫感染的抗原检测方法
- 批准号:
10082042 - 财政年份:2018
- 资助金额:
$ 69.21万 - 项目类别:
Diagnostic Assays for early Lyme Borreliosis using in-vivo expressed antigens
使用体内表达抗原诊断早期莱姆疏螺旋体病
- 批准号:
8876556 - 财政年份:2014
- 资助金额:
$ 69.21万 - 项目类别:
A Lyme disease vaccine using newly identified in-vivo expressed antigens
使用新鉴定的体内表达抗原的莱姆病疫苗
- 批准号:
8455815 - 财政年份:2013
- 资助金额:
$ 69.21万 - 项目类别:
A Lyme disease vaccine using newly identified in-vivo expressed antigens
使用新鉴定的体内表达抗原的莱姆病疫苗
- 批准号:
8601286 - 财政年份:2013
- 资助金额:
$ 69.21万 - 项目类别:
Diagnostic Assays for early Lyme Borreliosis using in-vivo expressed antigens
使用体内表达抗原诊断早期莱姆疏螺旋体病
- 批准号:
8782201 - 财政年份:2012
- 资助金额:
$ 69.21万 - 项目类别:
Diagnostic Assays for early Lyme Borreliosis using in-vivo expressed antigens
使用体内表达抗原诊断早期莱姆疏螺旋体病
- 批准号:
8315248 - 财政年份:2012
- 资助金额:
$ 69.21万 - 项目类别:
A serologic assay to measure successful Lyme borreliosis antibiotic therapy
测量莱姆疏螺旋体病抗生素治疗是否成功的血清学检测
- 批准号:
8715103 - 财政年份:2010
- 资助金额:
$ 69.21万 - 项目类别:
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