NeuroCovid Autoantibodies: Establishing a research pipeline
NeuroCovid Autoantibodies: Establishing a research pipeline
批准号:
10291218
负责人:
SAMUEL JEREMY PLEASURE
金额:
$32.3万
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:
2007-09-01 至 2021-03-31
关键词:
2019-nCoVAcuteAntibodiesAntigensAntiviral AgentsAutoantibodiesAutoantigensAutoimmuneAutoimmunityBiological AssayBiological MarkersBrainBrain Hypoxia-IschemiaCOVID-19COVID-19 patientCOVID-19 screeningCellsCerebrospinal FluidChildChronicClinicalClinical ManagementClinical ResearchCollaborationsCollectionComplexCustomDataDecision MakingDetectionDevelopmentDiseaseEmergency SituationEncephalitisEncephalopathiesEnrollmentFundingGeneral HospitalsGuillain Barré SyndromeHealthHumanHuman ResourcesImmuneImmunofluorescence ImmunologicImmunoglobulin GImmunoprecipitationImmunosuppressionIncubatedInfectionInflammationInflammatoryInfrastructureKidney FailureLaboratoriesLibrariesMaintenanceMass Spectrum AnalysisMediatingMedical centerMetagenomicsMoodsMusNational Institute of Allergy and Infectious DiseaseNeuraxisNeurologicNeurologistNeuropathogenesisOutpatientsPathogenesisPatientsPediatric HospitalsPeripheralPersonalityPhage DisplayPhage ImmunoPrecipitation SequencingPhenotypeProcessProteomeProtocols documentationResearchResearch PersonnelSARS-CoV-2 infectionSamplingSan FranciscoScientistSeminomaStainsSteroidsStrokeSyndromeSystemic diseaseTestingTherapeuticThrombophiliaTimeTissuesTransfectionUnited States National Institutes of HealthUniversitiesViralWorkacute flaccid myelitisbaseclinical phenotypeclinically actionablecohortexperimental studyfollow-upinnovationinsightmenneuroinflammationneuromechanismnext generation sequencingnovelnovel coronaviruspleasureprogramsprospectiverelating to nervous system
中文摘要
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英文摘要
PROJECT ABSTRACT
COVID-19 is associated with a growing number of peripheral and central nervous system complications.
It has become clear that a subset of these syndromes, including acute necrotizing encephalopathy, steroid-
responsive encephalitis and Guillain-Barré syndrome, are likely due autoimmunity triggered by SARS-CoV-2
infection. There is an urgent need to prospectively investigate the acute and chronic neurologic complications of
COVID-19 and determine which syndromes are neuroinflammatory in origin — particularly those caused by para-
infectious autoimmunity. While anti-viral therapeutics are still being developed for SARS-CoV-2, autoimmune
CNS conditions can be very responsive to immunosuppression. Thus, identifying biomarkers for a subset of
COVID-19 patients with autoimmune CNS syndromes could immediately impact clinical management.
Over the past 7 years, a unique interdisciplinary team of neurologists and basic scientists at UCSF was
formed to develop and deploy an integrated approach to rapidly anti-neural antibodies associated with
encephalitis, with the explicit intent to discover and validate clinically actionable biomarkers in addition to
uncovering the fundamental mechanisms of disease pathogenesis underlying these syndromes. The
centerpiece of these efforts is an ongoing patient cohort called the NID (Neuroinflammatory Disease) cohort,
consisting of patients with suspected infectious or inflammatory encephalitis. This cohort is now >1,500
patients referred by clinicians at UCSF and from other centers around the world. Already, this cohort has
spurred the development of the first ever clinically validated cerebrospinal fluid metagenomic next-generation
sequencing assay, the identification of a novel paraneoplastic autoimmune syndrome with important
implications for men with seminoma and the identification of enteroviral CSF antibodies in children with acute
flaccid myelitis. Here, we propose to adapt this existing clinical research and laboratory infrastructure to
enroll and investigate the urgent question whether COVID-19 patients with ongoing neurologic
sequelae have CNS inflammation. We will perform this work in collaboration with colleagues at the NIH,
Yale University as well as at UCSF Medical Center, Zuckerberg San Francisco General Hospital and
UCSF Benioff Children's Hospital. We seek emergency funding to accelerate our work on identifying anti-
neural autoantibodies associated with SARS-CoV-2 infection in patients with neurologic syndromes in 1
immediate aim.
Aim 1: Identify autoantibodies in the CSF of COVID-19 patients with neurologic syndromes.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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批准号:10387637
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项目类别:
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资助金额:$62.35万
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财政年份:2022
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负责人:SAMUEL JEREMY PLEASURE
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依托单位:
Humoral Immune Mechanisms of Acute and Chronic Neurologic Sequelae of COVID-19
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批准号:10573297
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项目类别:
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依托单位:
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批准号:9896570
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项目类别:
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资助金额:$40.38万
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财政年份:2020
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负责人:SAMUEL JEREMY PLEASURE
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依托单位:
NMDA receptors and callosal circuitry: development and molecular mechanisms
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批准号:10612860
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项目类别:
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资助金额:$40.38万
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财政年份:2020
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负责人:SAMUEL JEREMY PLEASURE
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依托单位:
Predoctoral Training in Neurobiology
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批准号:10210315
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项目类别:
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资助金额:$46.03万
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财政年份:2020
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负责人:SAMUEL JEREMY PLEASURE
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依托单位:
Predoctoral Training in Neurobiology
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批准号:10621344
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项目类别:
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资助金额:$50.05万
-
财政年份:2020
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负责人:SAMUEL JEREMY PLEASURE
-
依托单位:
NMDA receptors and callosal circuitry: development and molecular mechanisms
-
批准号:10393520
-
项目类别:
-
资助金额:$40.38万
-
财政年份:2020
-
负责人:SAMUEL JEREMY PLEASURE
-
依托单位:
Predoctoral Training in Neurobiology
-
批准号:10414948
-
项目类别:
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资助金额:$49.3万
-
财政年份:2020
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负责人:SAMUEL JEREMY PLEASURE
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依托单位:
Exploiting the hair-brain connection to treat perinatal brain disease
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批准号:8173388
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项目类别:
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资助金额:$30.9万
-
财政年份:2011
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负责人:SAMUEL JEREMY PLEASURE
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依托单位:
Exploiting the hair-brain connection to treat perinatal brain disease
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批准号:8412155
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项目类别:
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资助金额:$8.65万
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财政年份:2011
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负责人:SAMUEL JEREMY PLEASURE
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依托单位:
Exploiting the hair-brain connection to treat perinatal brain disease
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批准号:8468762
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项目类别:
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资助金额:$36.78万
-
财政年份:2011
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负责人:SAMUEL JEREMY PLEASURE
-
依托单位:
Exploiting the hair-brain connection to treat perinatal brain disease
-
批准号:8300820
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项目类别:
-
资助金额:$30.9万
-
财政年份:2011
-
负责人:SAMUEL JEREMY PLEASURE
-
依托单位:
Exploiting the hair-brain connection to treat perinatal brain disease
-
批准号:8662328
-
项目类别:
-
资助金额:$30.59万
-
财政年份:2011
-
负责人:SAMUEL JEREMY PLEASURE
-
依托单位:
Distinct Embryonic Origin for Postnatal Dentate Neural Stem Cells
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批准号:8502553
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项目类别:
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资助金额:$37.08万
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财政年份:2007
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负责人:SAMUEL JEREMY PLEASURE
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依托单位:
Control of dentate neurogenesis: Shh, mossy cells, activity and seizures
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批准号:10593970
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项目类别:
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资助金额:$37.95万
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财政年份:2007
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负责人:SAMUEL JEREMY PLEASURE
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依托单位:
Control of dentate neurogenesis: Shh, mossy cells, activity and seizures
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批准号:10444581
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项目类别:
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资助金额:$2.06万
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财政年份:2007
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负责人:SAMUEL JEREMY PLEASURE
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依托单位:
Forced Differentiation of CNS Neural Precursors in vitro and in vivo
-
批准号:7259318
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项目类别:
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资助金额:$20.19万
-
财政年份:2007
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负责人:SAMUEL JEREMY PLEASURE
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依托单位:
SDF1/CXCR4 Signaling and Tangential Neuronal Migration in the Developing Cortex
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批准号:8097474
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项目类别:
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资助金额:$34.41万
-
财政年份:2007
-
负责人:SAMUEL JEREMY PLEASURE
-
依托单位:
Distinct Embryonic Origin for Postnatal Dentate Neural Stem Cells
-
批准号:8688056
-
项目类别:
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资助金额:$38.63万
-
财政年份:2007
-
负责人:SAMUEL JEREMY PLEASURE
-
依托单位:
海外基金