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NeuroCovid Autoantibodies: Establishing a research pipeline

NeuroCovid Autoantibodies: Establishing a research pipeline
NeuroCovid 自身抗体:建立研究渠道
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

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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.
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