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Application of Novel Antigens and Integrated Microfluidics for Leprosy Diagnosis

Application of Novel Antigens and Integrated Microfluidics for Leprosy Diagnosis
新型抗原和集成微流控技术在麻风病诊断中的应用
批准号:
8133489
负责人:
ROBERT L MODLIN
金额:
$34.3万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-28 至 2014-08-31
关键词:
AddressAllelesAntibodiesAntibody FormationAntigensAreaBacillus (bacterium)BacteriaBacteriologyBindingBiochemicalBioinformaticsBiological AssayBlood specimenCD4 Positive T LymphocytesCharacteristicsChemoprophylaxisClassificationClinicalCommunicable DiseasesContractsControl GroupsDetectionDeveloping CountriesDevelopmentDiagnosisDiagnosticDiagnostic testsDiseaseDisease ProgressionEarly DiagnosisEconomic BurdenEnsureEpidemiologyEpitopesEyeFocal InfectionFrequenciesFundingGenerationsGeneticGlycolipidsGlycopeptidesGlycoproteinsGoalsHLA-DR AntigensHistocompatibility Antigens Class IIHumanHumoral ImmunitiesImmuneImmune responseImmunologicsImmunologyIncidenceIndividualInfectionInterferonsInterleukin-10Interleukin-2Interleukin-4Interleukin-5InvadedInvestigationLaboratoriesLepromatous LeprosyLeprosyLesionLimb structureLipoprotein (a)MeasuresMicrobeMicrofluidicsMolecular BiologyMorphologyMycobacterium lepraeNational Institute of Allergy and Infectious DiseaseNerveNeurologic DeficitOutcomePatientsPatternPeptidesPopulationProgressive DiseaseProtein GlycosylationProteinsPublic HealthRecombinantsResearch PersonnelResourcesRiskScreening procedureSensitivity and SpecificitySerumSkinSourceStagingT cell responseT-LymphocyteTechnologyTestingToll-like receptorsTropical DiseaseTuberculoid leprosyTuberculosisUnited States National Institutes of Healthbasecell mediated immune responsechemotherapycytokinedisabilitydisease classificationdisorder preventionfundamental researchhealth economicshigh riskimprovedinsightlight microscopymeetingsmicrobialneglectnew technologynovelnovel diagnosticspathogenperipheral bloodportabilitypreventresponseskin lesiontransmission process

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DESCRIPTION (provided by applicant): The overall objective of this application is to develop a specific and simple diagnostic test to identify individuals infected with Mycobacterium leprae and therefore sources of continuing new case detection, enabling rational chemoprophylaxis of leprosy leading not only to decrease in infectious burden but in reductions in nerve damage and disabilities. We hypothesize that such a diagnostic test can be achieved by measuring the immunologic response patterns to specific M. leprae antigens in peripheral blood samples from patients and contacts. The specific aims of this proposal are to: 1) develop a specific and simple first generation diagnostic test using advanced bioinformatics to identify M. leprae-specific peptides predicted to bind to 11 major HLA-DR alleles and to activate T-cell release of IFN-, to be incorporated into the QuantiFERON(R) platform; 2) To identify novel M. leprae antigens, including glycoproteins and lipoglycoproteins, that trigger innate and acquired immune responses during infection; and, 3) to develop an advanced integrated microfluidics-based portable diagnostic test to simultaneously measure multiple immunologic parameters providing enhanced specificity, sensitivity, and, perhaps, predictions of disease. The proposed experimental strategy will ensure development of a portable, state-of-the-art diagnostic test to detect M. leprae infection, identify sources of continuing new cases but also a new technology platform that can be readily adapted to implementation in leprosy endemic areas and to other neglected tropical infectious diseases. H Leprosy continues as a major health and economic burden in developing countries. We propose to develop a microfluidics-based portable diagnostic test to allow diagnosis of infection and sources of continuing transmission, allowing informed chemoprophylaxis and thereby further reduction in the global leprosy burden including disease complications including permanent damage to the skin, nerves, limbs and eyes.
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