Mechanisms by which M. tuberculosis 13KDa lectin modulates human immune responses
Mechanisms by which M. tuberculosis 13KDa lectin modulates human immune responses
批准号:
8508839
负责人:
Andre Bafica
金额:
$4.99万
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:
2009-09-01 至 2015-08-31
关键词:
AgonistAntibiotic TherapyAntigen-Presenting CellsAntitubercular AgentsBacteriaBindingBiochemicalBioinformaticsBiological MarkersBlocking AntibodiesBrazilC Type Lectin ReceptorsC-Type LectinsCD209 geneCD80 geneCell CommunicationCell Culture TechniquesCell LineCell physiologyCellsCitiesCoculture TechniquesCommunicable DiseasesConfocal MicroscopyCytokine GeneCytometryDataData AnalysesDatabasesDendritic CellsDevelopmentDiagnosticDiseaseEnzyme-Linked Immunosorbent AssayErythrocytesExposure toFamilyFlow CytometryGene ExpressionGenesGenus MycobacteriumGoalsGreen Fluorescent ProteinsHealthHost resistanceHumanImmune responseImmune systemImmunityImmunoglobulin GImmunologic ReceptorsImmunotherapyIn VitroInfectionInflammation MediatorsInflammatoryInterferon Type IIInterleukin-10Interleukin-12Interleukin-17Interleukin-6KnowledgeLectinLung diseasesMHC Class II GenesMacrophage-1 AntigenMeasuresMembraneModelingMonoclonal AntibodiesMusMycobacterium smegmatisMycobacterium tuberculosisOutcomeOutcome StudyPathogenesisPathway interactionsPatient MonitoringPatientsPatternPeripheral Blood Mononuclear CellPhagocytosisPlayPreparationProcessProductionProtein Binding DomainProteinsPublishingReagentRecombinantsResearchRicinRoleSerumSurfaceSystemT-Cell ProliferationT-LymphocyteTLR2 geneTLR3 geneTLR4 geneTLR7 geneTNF geneTNFRSF5 geneTestingTimeToll-like receptorsTuberculosisVirulenceWorkbasechemotherapycohortcytokinedectin 1glucan phosphateimmunoprophylaxisimprovedin vivointerestinterleukin-23laminaranmacrophagemonocytemycobacterialneutralizing antibodynovelpathogenprotein protein interactionreceptorreceptor expressionresearch studyresponsescreeningstemsugartooltuberculosis treatmentuptake
中文摘要
结核分枝杆菌13 kDa凝集素调控人类的机制
免疫反应
项目摘要
结核分枝杆菌新蛋白的研究可能是
改进结核病的诊断工具、治疗和免疫预防,
这是世界上最流行的传染病之一。我们已经确认了一只13 KDa的
结核分枝杆菌中的类似蓖麻毒素的凝集素,被发现能凝集红细胞和
巨噬细胞诱导细胞因子表达。此外,活动性肺结核患者的血清
患者体内有较高水平的抗该凝集素的抗体。在目前的提案中,我们的目标是
研究13 KDa Mtb凝集素在人体免疫应答中的作用。具体的
这项研究的目的是1)描述先天免疫反应的特征
13 KDa Mtb凝集素;2)人天然受体(S)的测定
APC参与13 KDa Mtb凝集素的识别;3)研究13
KDA Mtb凝集素在人感染/吞噬结核分枝杆菌过程中的作用
APC和4)检测针对13的特异性体液和细胞免疫反应
结核患者抗生素治疗前后KDA、Mtb、凝集素的变化我们的长期合作
目的是确定13 KDa的蓖麻毒素样凝集素是否在调节人类
结核的免疫反应侧重于它在控制APC功能中的可能活动。
这些研究可能对揭示免疫治疗的新靶点具有重要意义。
肺结核。
英文摘要
Mechanisms by which M. tuberculosis 13 kDa lectin modulates human
immune responses
Project Summary
Study of novel proteins from Mycobacterium tuberculosis may be a critical step for
improving diagnostic tools, therapies and immunoprophylaxis against tuberculosis (TB),
one of the most prevalent infectious diseases wordwide. We have identified a 13 KDa
ricin-like lectin from M. tuberculosis that was found to agglutinate red blood cells and
induce cytokine expression by macrophages. Moreover, serum from active tuberculosis
patients contained high levels of IgG against this lectin. In the present proposal, we aim
to characterize the role of 13 KDa Mtb lectin on human immune responses. The specific
aims of the study are to 1) characterize the innate immune response profile elicited
by the 13 KDa Mtb lectin; 2) determine innate receptor(s) expressed on human
APC involved in the recognition of 13 KDa Mtb lectin; 3) investigate the role of 13
KDa Mtb lectin in the infection/phagocytosis process of M. tuberculosis by human
APC and 4) examine specific humoral and cellular immune responses against 13
KDa Mtb lectin in TB patients before and after antibiotic treatment. Our long-term
goal is to determine whether 13 KDa Mtb ricin-like lectin plays a role in regulating human
immune responses to TB focusing on it possible activity in controlling APC function.
These studies could be important in revealing a new target for immunotherapy of
tuberculosis.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Mechanisms by which M. tuberculosis 13KDa lectin modulates human immune responses
-
批准号:8311544
-
项目类别:
-
资助金额:$5.31万
-
财政年份:2009
-
负责人:Andre Bafica
-
依托单位:
Mechanisms by which M. tuberculosis 13KDa lectin modulates human immune responses
-
批准号:7688816
-
项目类别:
-
资助金额:$5.28万
-
财政年份:2009
-
负责人:Andre Bafica
-
依托单位:
Mechanisms by which M. tuberculosis 13KDa lectin modulates human immune responses
-
批准号:7922655
-
项目类别:
-
资助金额:$5.17万
-
财政年份:2009
-
负责人:Andre Bafica
-
依托单位:
Mechanisms by which M. tuberculosis 13KDa lectin modulates human immune responses
-
批准号:8712591
-
项目类别:
-
资助金额:$5.35万
-
财政年份:2009
-
负责人:Andre Bafica
-
依托单位:
海外基金