Immunologic basis of cardiac disease after severe COVID-19
Immunologic basis of cardiac disease after severe COVID-19
批准号:
10442251
负责人:
Jason V Baker
金额:
$69.46万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2022
资助国家:
美国
项目状态:
未结题
起止时间:
2022-07-01 至 2026-05-31
关键词:
2019-nCoVAcuteAdmission activityAwardBiological MarkersBlood specimenCD4 Positive T LymphocytesCOVID-19COVID-19 patientCOVID-19 survivorsCardiacCardiologyCardiomyopathiesCardiopulmonaryCardiovascular systemCellsChronicClinicalCommunicable DiseasesDiffuseEndothelial CellsEnrollmentEpidemicEpidemiologyFibroblastsFibrosisFrequenciesFunctional disorderGoalsHealthHeart AbnormalitiesHeart DiseasesHeart InjuriesHospitalizationImmuneImmune responseImmunofluorescence ImmunologicImmunologicsImmunologyIn VitroInfectionInflammationInflammatoryInfluenzaInjuryInterventionKnowledgeLate EffectsLifeLong COVIDLow PrevalenceLymphopeniaMagnetic ResonanceMeasuresMediatingMicrocirculationMononuclearMuscle CellsMyocardialMyocardial dysfunctionMyocarditisNatural ImmunityOrganParticipantPathologyPatientsPeptidesPericytesPhenotypePost-Acute Sequelae of SARS-CoV-2 InfectionProteinsProtocols documentationRecoveryReportingResearchRespiratory DiseaseRespiratory FailureSARS-CoV-2 infectionScienceSpecialistSpecimenSurvivorsSymptomsT cell responseT-LymphocyteTestingTissuesTroponinViralVirus DiseasesWorkadaptive immune responsebasecardiac magnetic resonance imagingcardiovascular effectscardiovascular injuryclinically relevantcohortcoronary fibrosiscoronavirus diseasecytokinedisabilityexperienceheart damageimmune activationimprovedinfluenza infectioninjured airwaymacrophagemonocytemyocardial injuryneutrophilnovelpandemic diseaseparticlepersistent symptomreceptorresponserisk stratificationsevere COVID-19spatial relationshipstudy populationsystemic inflammatory responsethrombotic complicationswound healing
中文摘要
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英文摘要
ABSTRACT
Coronavirus Disease 2019 (COVID-19) caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-
CoV-2) has become a widespread global pandemic. While the predominant clinical manifestation of severe
COVID-19 is respiratory failure, other organ complications such as cardiac injury are common. Cardiac injury
and cardiomyopathy are frequent cardiac manifestations during acute illness. Additionally, some survivors of
COVID-19 are experiencing cardiopulmonary symptoms months after the acute illness, referred to as Post-
Acute Sequelae of SARS-CoV-2 (PASC) or “Long COVID”. Given the frequency of cardiovascular injury during
COVID-19 and the persistence of symptoms for extended periods after the acute illness, there is an urgent
need for studies of the late effects of SARS-CoV-2 on the cardiovascular system. We aim to investigate the
central hypothesis that immune responses to severe COVID-19 cause acute inflammation and injury that result
in clinically relevant myocardial fibrosis and dysfunction over the long-term. Since August 2020, we have been
enrolling patients in a COVID-19 Immune Profiling (IP) Study, which includes a protocol to collect blood
specimens from patients with COVID-19 at admission, during hospitalization, 1-3 months, and 3-12 months
after recovery. We will co-enroll participants from this study and perform cardiac magnetic resonance imaging
(CMR) and additional functional cardiopulmonary assessments at 3-12 months and 2-3 years after recovery.
Our specific aims include, Aim 1) Identify innate immune profiles during severe COVID-19 that predict long-
term cardiac damage. We will focus innate immunity measures in blood specimens collected at admission and
early recovery, Aim 2) Establish whether adaptive immune responses contribute to cardiac injury after COVID-
19. We will quantify responses targeting SARS-CoV-2 as well as explore maladaptive responses targeting
cardiac proteins. Analysis of blood specimens will be supplemented with exploratory studies of cardiac tissue,
and Aim 3) Determine the long-term structural and functional cardiac abnormalities after severe COVID-19.
This includes characterization of cardiac fibrosis and dysfunction, cardiopulmonary dysfunction, and clinical
symptoms. Comparisons will be made with control participants who had influenza infection 1-2 years prior. Our
proposal responds to urgent need for science characterizing long-term cardiac complications following COVID-
19. Our collaborative team has extensive experience spanning cardiology, infectious disease, immunology,
and epidemiology, and will be led by a cardiologist with expertise in CMR and inflammatory cardiomyopathies,
and an infectious diseases specialist with expertise in cardiovascular complications in the context of chronic
viral infections. Successful completion of our work will help understand the long-term cardiovascular effects of
severe COVID-19 illness. This knowledge could, in turn, help enhance health, lengthen life, and reduce illness
and disability in COVID-19 survivors.
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Immunologic basis of cardiac disease after severe COVID-19
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批准号:10685376
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财政年份:2019
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批准号:8641495
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财政年份:2014
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批准号:9038208
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资助金额:$55.9万
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财政年份:2014
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依托单位:
Treatment to reduce inflammation and improve immune recovery among older HIV pts
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批准号:8883185
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项目类别:
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资助金额:$5.25万
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财政年份:2014
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依托单位:
Targeted anticoagulant therapy to reduce inflammation in treated HIV disease
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批准号:8846913
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资助金额:$63.86万
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财政年份:2014
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负责人:Jason V Baker
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依托单位:
Targeted anticoagulant therapy to reduce inflammation in treated HIV disease
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批准号:9281047
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项目类别:
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资助金额:$43.33万
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依托单位:
Targeted anticoagulant therapy to reduce inflammation in treated HIV disease
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批准号:9068239
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项目类别:
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资助金额:$66.79万
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负责人:Jason V Baker
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依托单位:
海外基金