Novel Immunotherapy of African Trypanosomiasis
Novel Immunotherapy of African Trypanosomiasis
批准号:
7386897
负责人:
John M. Mansfield
金额:
$22.05万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-12-01 至 2009-11-30
关键词:
AffectAfricanAfrican TrypanosomiasisAgonistAnimalsAntigenic VariationAntigensBiologicalCellsDataDefectDiseaseElementsEventGene ActivationGenerationsGenesGeneticHost resistanceHumanImageImmuneImmune systemImmunityImmunosuppressionImmunotherapyIndividualInfectionInfection ControlInterferonsInvestigational TherapiesKineticsLeadLinkMeasuresMethodsMicroarray AnalysisMonitorMusNatural ImmunityParasite ControlParasitesParasitic DiseasesPathway interactionsProductionPublic HealthRelative (related person)Research Project GrantsResistanceSignal PathwaySignal TransductionT-LymphocyteTestingTherapeutic EffectTherapeutic immunosuppressionTimeTissuesTrypanosomaTrypanosoma brucei rhodesienseTrypanosomiasisbasechemotherapydisorder controlgenetic linkageinnovationnovelnovel therapeuticsresistance mechanismresponse
中文摘要
描述(由申请人提供):这是一项探索性研究资助,旨在开发一种治疗非洲锥虫病的新型治疗方法,这是一种致命的人类寄生虫病,已被证明是传统免疫疗法难以治愈的。本提案探讨了新的和令人兴奋的结果,CpG寡脱氧核苷酸(ODN)治疗显着增强宿主的抗锥虫。生物学效应包括显著增加宿主存活率、减少寄生虫负担、增强先天免疫和适应性免疫以及改变寄生虫细胞分化。
因此,本研究的目的是阐明最佳CpG ODN治疗实验性锥虫病的动力学、广度和潜在机制。特异性目的1通过测量锥虫组织侵入、组织特异性基因活化、先天性免疫细胞刺激和寄生虫特异性B和T细胞应答的控制来检查受感染宿主中CpG ODN诱导的改变。特异性目的2测试了TLR 9-、MyD 88-和IRF 7-依赖性I型IFN(IFN-1/2)途径的扩增是CpG ODN增强宿主抗性的基础的机制假设。另一种假设是,CpG ODN治疗放大了先天免疫系统产生的II型IFN(IFN-3),调节锥虫细长短的细胞分化和宿主抗性。
总的来说,这些新的和令人兴奋的研究提供了一种新的治疗方法来控制非洲锥虫病,避免了许多复杂的问题,目前这种疾病的治疗。
这个探索性项目提出了一种控制或治疗非洲锥虫病(一种致命的人类寄生虫病)的创新方法。成功完成这些目标将使公共卫生官员能够用CpG寡脱氧核苷酸治疗锥虫感染者,这将激活先天免疫系统的关键组成部分,以控制疾病。
英文摘要
DESCRIPTION (provided by applicant): This is an exploratory research grant that develops a novel therapeutic approach for treating African trypanosomiasis, a fatal human parasitic disease that has proven intractable to conventional immunotherapy. The present proposal examines the novel and exciting result that CpG oligodeoxynucleotide (ODN) treatment significantly enhances host resistance to trypanosomiasis. The biological effects include a marked increase in host survival, decreased parasite burden, enhanced innate and adaptive immunity, and alterations in parasite cellular differentiation.
Therefore, the aims of this proposal are to elucidate the kinetics, breadth and the underlying mechanism of optimal CpG ODN therapy of experimental trypanosomiasis. Specific Aim 1 examines CpG ODN-induced alterations in the infected host by measuring control of trypanosome tissue invasion, tissue-specific gene activation, innate immune cell stimulation, and parasite- specific B and T cell responses. Specific Aim 2 tests the mechanistic hypothesis that amplification of the TLR9-, MyD88- and IRF7-dependent Type I IFN (IFN-1/2) pathway underlies CpG ODN enhancement of host resistance. An alternative hypothesis is also presented in which CpG ODN treatment amplifies innate immune system production of Type II IFN (IFN-3) which regulates trypanosome long-slender to short-stumpy cellular differentiation and host resistance.
Overall, these novel and exciting studies provide a new therapeutic approach to controlling African trypanosomiasis that avoids many of the issues complicating current therapy of this disease.Project Narrative
This exploratory project proposes an innovative approach to the control or cure of African trypanosomiasis, a fatal human parasitic disease. Successful completion of the aims will enable public health officers to treat trypanosome infected individuals with CpG oligodeoxynucleotides which will activate critical components of the innate immune system to control the disease.
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Cross-Protective Immunity to African Trypanosomes
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批准号:8033918
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项目类别:
-
资助金额:$21.89万
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财政年份:2011
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负责人:John M. Mansfield
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依托单位:
Cross-Protective Immunity to African Trypanosomes
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批准号:8414204
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项目类别:
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资助金额:$18.17万
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财政年份:2011
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负责人:John M. Mansfield
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依托单位:
Novel Immunotherapy of African Trypanosomiasis
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批准号:7534762
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项目类别:
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资助金额:$18.38万
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财政年份:2007
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负责人:John M. Mansfield
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依托单位:
BIOLOGICAL VARIATION AMONG AFRICAN TRYPANOSOMES
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批准号:6046113
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项目类别:
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资助金额:$25.0万
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财政年份:2000
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负责人:John M. Mansfield
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依托单位:
BIOLOGICAL VARIATION AMONG AFRICAN TRYPANOSOMES
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批准号:6349827
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项目类别:
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资助金额:$25.75万
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财政年份:2000
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负责人:John M. Mansfield
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依托单位:
BIOLOGICAL VARIATION AMONG AFRICAN TRYPANOSOMES
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批准号:6497078
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项目类别:
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资助金额:$26.53万
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财政年份:2000
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负责人:John M. Mansfield
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依托单位:
BIOLOGICAL VARIATION AMONG AFRICAN TRYPANOSOMES
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批准号:2076258
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项目类别:
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资助金额:$15.75万
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财政年份:1996
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负责人:John M. Mansfield
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依托单位:
IMMUNOBIOLOGY OF AFRICAN TRYPANOSOMIASIS
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批准号:2061814
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项目类别:
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资助金额:$27.28万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
IMMUNOBIOLOGY OF AFRICAN TRYPANOSOMIASIS
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批准号:3133501
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项目类别:
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资助金额:$16.46万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
IMMUNOBIOLOGY OF AFRICAN TRYPANOSOMIASIS
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批准号:6011839
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项目类别:
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资助金额:$33.21万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
TROPICAL MEDICINE AND PARASITIOLOGY STUDY SECTION
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批准号:3555240
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项目类别:
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资助金额:$5.78万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
IMMUNOBIOLOGY OF AFRICAN TRYPANOSOMIASIS
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批准号:3133497
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项目类别:
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资助金额:$24.24万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
TROPICAL MEDICINE AND PARASITIOLOGY STUDY SECTION
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批准号:3555239
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项目类别:
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资助金额:$7.5万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
IMMUNOBIOLOGY OF AFRICAN TRYPANOSOMIASIS
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批准号:2061812
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项目类别:
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资助金额:$25.16万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
IMMUNOBIOLOGY OF AFRICAN TRYPANOSOMIASIS
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批准号:3133495
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项目类别:
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资助金额:$17.56万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
IMMUNOBIOLOGY OF AFRICAN TRYPANOSOMIASIS
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批准号:3133493
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项目类别:
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资助金额:$26.57万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
IMMUNOBIOLOGY OF AFRICAN TRYPANOSOMIASIS
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批准号:2390288
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项目类别:
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资助金额:$28.37万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
IMMUNOBIOLOGY OF AFRICAN TRYPANOSOMIASIS
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批准号:6373067
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项目类别:
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资助金额:$33.5万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
IMMUNOBIOLOGY OF AFRICAN TRYPANOSOMIASIS
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批准号:6510335
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项目类别:
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资助金额:$34.5万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
TROPICAL MEDICINE AND PARASITOLOGY STUDY SECTION
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批准号:3555242
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项目类别:
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资助金额:$3.59万
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财政年份:1985
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负责人:John M. Mansfield
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依托单位:
海外基金