Novel Therapeutic Approaches to Tuberculosis
Novel Therapeutic Approaches to Tuberculosis
批准号:
8650487
负责人:
DAVID L. WOODLAND
金额:
$0.8万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-02-01 至 2015-01-31
关键词:
AcuteAnimal ModelAnti-Bacterial AgentsAreaBacteriaBacteriologyBasic ScienceBiologicalCause of DeathCellular biologyClinical ResearchCollaborationsColoradoCommunicable DiseasesDevelopmentDiseaseEnsureFosteringGleanGoalsHIVHumanImmunityImmunologyImmunotherapyInfectionInflammationInflammatory ResponseInstitutionInterventionLungMalariaMalignant NeoplasmsMycobacterium tuberculosisOutcomePharmaceutical PreparationsPhysiologyPopulationRegimenResearchResearch PersonnelRoleScientistSolutionsSpeedSystemTherapeuticTuberculosisVaccinesVirus Diseasesantimicrobialbasecareer developmentchemical geneticschemotherapycytokinedesigndisorder controldisorder riskdrug developmentdrug discoveryinsightkillingsmeetingsmicrobialmycobacterialnext generationnovel strategiesnovel therapeutic interventionnovel therapeuticspathogenplanetary Atmospherepublic health relevanceresponsesuccesssymposiumtherapeutic developmenttherapeutic vaccinetransmission processtuberculosis treatmentvaccine development
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Support is requested for a Keystone Symposia meeting entitled Novel Therapeutic Approaches to Tuberculosis, organized by Christopher M. Sassetti and Thomas G. Evans. The meeting will be held in Keystone, Colorado from March 30 - April 4, 2014. Despite more than a century of research, tuberculosis kills millions every year. The reasons we are unable to control this disease are well documented: the lack of an effective vaccine, inefficient chemotherapy, and an inability to predict who is at risk of disease. Traditionl approaches to antibacterial and vaccine development have produced only incremental improvements in TB therapy, and have had little effect on transmission in the developing world. This meeting will explore novel strategies to treat this disease, either through direct antimicrobil interventions or the manipulation of host immunity. Plenary sessions will explore three topical areas: 1) The mechanisms underlying the inflammatory response to M. tuberculosis, and novel strategies to ameliorate disease through the manipulation of this response; 2) New approaches to accelerate TB chemotherapy, concentrating on genetic/chemical synergies, specific targeting of persistent bacterial populations, and host-directed antimicrobial therapies; and 3) Immunotherapy for both latent and active disease, with an emphasis on cytokine modulation and therapeutic vaccines. This symposium will assemble a diverse group of scientists specializing in immunology, bacteriology, cell biology, and therapeutic development. To ensure that insights from basic science are discussed in the context of practical therapeutic solutions, attendees will be drawn from both academic and industrial institutions. A particular emphasis will be placed on lessons gleaned from other systems, such as cancer, acute inflammation, and viral infections, which could be applied to tuberculosis. This diversity of background and approach will encourage the development of truly novel approaches to treat this devastating disease.
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