Type I Interferon: Friend and Foe Alike
Type I Interferon: Friend and Foe Alike
批准号:
9252754
负责人:
Thale Cross Jarvis
金额:
$0.9万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-01-01 至 2017-12-31
关键词:
AddressAlberta provinceAntineoplastic AgentsAntiviral AgentsAreaAutoimmune DiseasesAutoimmune ProcessBacterial InfectionsBacteriologyBiologyCanadaCancer BiologyCellsClinical ResearchCollaborationsCommunicable DiseasesDependencyDevelopmentDisciplineDiseaseEducational workshopFamilyFosteringFriendsFutureGene FamilyGenesGenetic ResearchGoalsHealthHereditary DiseaseHomeostasisHost DefenseHumanHuman GeneticsImmuneImmune System DiseasesImmunologicsImmunologistImmunologyIndustryInfectionInfectious AgentInflammationInflammation MediatorsInflammatoryInterdisciplinary StudyInterferon Type IInterferon-alphaInterferonsKnowledgeMalignant NeoplasmsMediatingMentorsMethodologyMolecularMolecular BiologyNatural ImmunityNeuronsOncogenicOncologistOutcomePathogenesisPathologicPathologyPathway interactionsPattern RecognitionPlayPostdoctoral FellowRegulationResearchResearch PersonnelRoleScienceScientistSignal PathwaySignal TransductionSolidStudentsSystemT cell responseTherapeutic InterventionTimeVaccinesViral PhysiologyVirginiaVirus Diseasesbaseclinical practicecontextual factorscytokinedesignhuman diseaseimmune functionimmunopathologyimmunoregulationimprovedinterestmeetingsnovel therapeuticspathogenpostersprospectiveresponsestructural biologysymposiumtargeted treatmenttranslational medicinevirology
中文摘要
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英文摘要
ABSTRACT
Support is requested for a Keystone Symposia meeting entitled Type I Interferon: Friend and Foe Alike,
organized by Drs. Alan Sher, Virginia Pascual, Adolfo García-Sastre and Anne O'Garra. The meeting will be
held in Banff, Alberta, Canada from March 19-23, 2017. While cytokines play critical roles in host defense and
immune homeostasis, they in other settings can be key mediators of inflammatory pathology. This important
functional dichotomy is perhaps best exemplified in the diverse activities of Type I interferon(s) in health and
disease. Type I IFNs regulate a broad family of genes that either stimulate or inhibit immune function and in so
doing have host protective or detrimental effects. Thus, while Type I IFNs are well-known for their anti-viral
activity and stimulation of effector T cell responses, they can also promote autoimmune, bacterial and even
certain viral diseases. Understanding this contextual dependency is crucial for unraveling the pathogenesis of
Type I IFN-dependent diseases and for the design of interferon-based therapies and will be the central focus of
the meeting. This conference will open with talks presenting an overview of Type I IFN genes and their
regulation, innate recognition mechanisms and signaling pathways for Type I IFN induction and Mendelian-
based interferonopathies. Additional sessions will focus on the role of Type I IFN in viral, bacterial and
autoimmune diseases. The meeting will conclude with a discussion of the mechanistic and contextual factors
that determine the beneficial versus deleterious outcome of Type I IFN induction and how this information can
be applied to the development of targeted therapeutic interventions. Because of the timeliness of the topic, the
conference should draw a broad audience from the fields of cytokine biology, inflammation, infectious disease
and translational medicine and attract a solid industry representation. Opportunities for interdisciplinary
interactions will be significantly enhanced by the concurrent meeting on Pattern Recognition Signaling: From
Innate Immunity to Inflammatory Disease, which will share a keynote address and plenary session with this
meeting.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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