Advancing Psychosocial and Biobehavioral Stress Measurement to Understanding Aging
Advancing Psychosocial and Biobehavioral Stress Measurement to Understanding Aging
批准号:
10630016
负责人:
Elissa S. Epel
金额:
$38.01万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-09-30 至 2024-06-30
关键词:
2019-nCoVAddressAdherenceAgeAgingAntibodiesAntibody ResponseBehavioralCOVID-19COVID-19 pandemicCOVID-19 vaccinationCellsCellular AssayCessation of lifeChronic stressCollecting CellData CollectionElderlyFreezingFundingImmuneImmune responseImmune systemImmunityImmunoglobulin GImmunologic MarkersIn VitroIndividualInfectionInfluenza vaccinationLengthLeukocytesMaintenanceMeasurementMeasuresMonoclonal Antibody R24MononuclearNucleocapsid ProteinsPeripheralPeripheral Blood Mononuclear CellPersonsPredictive FactorProcessPsychological FactorsPsychological StressPublic HealthResearch DesignSARS-CoV-2 infectionSamplingSecondary ImmunizationSeriesStressT cell responseTestingTimeVaccinationbasebiobehaviorbooster vaccinebreakthrough infectioncohortcoronavirus diseasecostdesignexperiencehigh riskimprovednovelpandemic diseaseparent grantpredictive testpreservationpsychosocialresponsesample collectionsocialtelomere
中文摘要
点击翻译按钮获取中文摘要
英文摘要
ABSTRACT
At this stage in the COVID-19 pandemic, a critical issue has become to understand how long individuals can
maintain strong immunity from vaccinations, which groups are at highest risk, and what malleable social,
behavioral, and psychological factors can promote optimal maintenance. Fortunately, due to our initial R24
supplement, we have launched a remarkable study (The BOOST Study) designed to address these questions
by examining telomere length, stress, and behavioral factors as predictors with 94% adherence. We have the
opportunity to examine response to a second vaccination with the same design in the same cohort, by adding
data collection six months after the booster vaccination. We will be the first study to be able to examine the
trajectory of immune responses at 3 critical post vaccination time points over the first year of vaccination roll
out. We can address our original predictors, leukocyte telomere length and chronic stress and age
interactions (Aims 1) as predictors of COVID-19 vaccination response trajectories (based on antibody
response at 6 weeks, and maintenance of antibodies at 6 months and now, newly, 6 months after booster
shot). Further, we can now test how these factors predict breakthrough infections (Aim 2). Lastly, this
supplement allows us to collect cells enabling us to apply for an R01 to examine T cell responses to
vaccination (Aim 3), a critical part of immune protection but rarely studied due to the costs of these in vitro
cell assays. Now that COVID-19 has become endemic, these questions are of critical importance to public
health for decades to come.
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海外基金