Immunological Phenotyping of Febrile and Afebrile Critically Ill Septic Patients
Immunological Phenotyping of Febrile and Afebrile Critically Ill Septic Patients
批准号:
9767817
负责人:
Anne Meredith Drewry
金额:
$17.83万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-09-01 至 2021-08-31
关键词:
AccountingAgeAnimalsAreaBiological MarkersBloodBody TemperatureCD28 geneCD3 AntigensCause of DeathCell surfaceClinicalClinical ResearchComputerized Medical RecordConsultationsCritical CareCritical IllnessCytomegalovirusDNADataDefectDevelopment PlansDiagnosisEnrollmentEnvironmentExhibitsFailureFeverFunctional disorderFundingGenerationsGoalsGrowthHLA AntigensHealthcareHospitalsHourHumanHuman Herpesvirus 4Human Herpesvirus 6Hypothalamic structureImmuneImmune System DiseasesImmunityImmunologicsImmunologyImmunophenotypingImmunosuppressionImpairmentIn VitroInfectionInflammationInflammatory ResponseInterdisciplinary StudyInterferon Type IIInterventionLaboratoriesLatent VirusLeadLinkLipopolysaccharidesLiteratureLymphocyte CountLymphopeniaMeasurementMeasuresMentored Patient-Oriented Research Career Development AwardMentorsMonitorMorbidity - disease rateMulticenter TrialsNatural ImmunityNosocomial InfectionsOutcomePatientsPhenotypePhysiologyPlayPredispositionProductionProspective cohort studyPublic HealthPublishingPyrogensRecoveryResearchResearch DesignResearch Project GrantsResearch SupportResearch TrainingRoleSepsisSeverity of illnessSimplexvirusT-LymphocyteTNF geneTechniquesTestingTherapeutic InterventionTimeTrainingUnited StatesUniversitiesViralVirus LatencyWashingtonWorkadaptive immunitybasecareer developmentcombatdesignhigh riskimmune functionimprovedinsightmonocytemortalitymultidisciplinarynovelpathogenpatient populationprospectivereactivation from latencyresponsesecondary infectionsepticseptic patientsstatisticstargeted treatmenttreatment strategytrial designtumor
中文摘要
点击翻译按钮获取中文摘要
英文摘要
PROJECT SUMMARY/ABSTRACT
Dr. Anne Drewry is an intensivist with the long-term goal of becoming an independently funded clinical trialist in
the field of critical care, with a focus on the role of body temperature in sepsis. Afebrile septic patients are twice
as likely to die than febrile patients, even after accounting for potentially confounding factors (e.g. age, illness
severity). Given the role of inflammation and immunity in the physiology of fever generation, immune dysfunction
is a potential link between failure to mount a fever and worse clinical outcomes. The objective of this proposal is
to determine whether immunological phenotypes differ between febrile and afebrile patients. The central hypoth-
esis is that septic patients who fail to mount a fever will demonstrate more severe sepsis-induced immune im-
pairment than febrile patients. This hypothesis is supported by the candidate’s preliminary data suggesting that
absence of fever is associated with impaired monocyte function and persistent lymphopenia, key mechanisms
of sepsis-induced immunosuppression. It will be tested by performing a prospective cohort study with the follow-
ing specific aims: (1) to determine whether febrile and afebrile septic patients exhibit differences in biomarkers
of sepsis-induced immunosuppression; and (2) to compare clinical signs of immunosuppression among febrile
and afebrile patients. Following enrollment, critically ill patients with severe sepsis will be divided into febrile and
afebrile groups based on the presence or absence of body temperature ≥ 38.0°C within 24 hours of sepsis
diagnosis. Sepsis-induced immunosuppression will be assessed via serial measurements of monocyte HLA-DR
expression, LPS-induced TNF-α production, anti-CD3/anti-CD28-induced IFN-γ production, and absolute lym-
phocyte counts. Clinical outcomes will include acquisition of secondary infections and reactivation of latent vi-
ruses. This work is significant because it is the first step in a continuum of research that is expected to lead to
targeted treatment of immune dysfunction in afebrile septic patients. The applicant will implement this project
with support from of her mentors (Drs. Richard Hotchkiss and Marin Kollef) and a multidisciplinary team of advi-
sors with expertise in sepsis immunology, clinical study design/execution, and statistics. The applicant, in con-
sultation with her mentors, has also designed a comprehensive career development plan emphasizing training
in the areas of (1) translational laboratory techniques, (2) adaptive trial design, (3) advanced statistics, and (4)
planning and execution of multicenter trials, with the goal of R01 submission prior the end of the K23 award
period. Given its high volume of critically ill patients and ample opportunities for research training and multidis-
ciplinary collaboration, Washington University is an ideal environment to support this research project and the
candidate’s overall career development.
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