T cell modulation of COVID-19 disease
T cell modulation of COVID-19 disease
批准号:
10239822
负责人:
Nicholas James Maness
金额:
$25.5万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-09-20 至 2023-08-31
关键词:
2019-nCoVAdult Respiratory Distress SyndromeAnimalsAntibodiesAntiviral AgentsBloodBlood Coagulation DisordersCD8-Positive T-LymphocytesCD8B1 geneCOVID-19COVID-19 pandemicCellsCessation of lifeComplementComplexCoronavirusDataDiseaseDisease OutcomeDisease ProgressionDisease modelEndothelial CellsExhibitsFutureGenerationsGeneticHumanHyperactivityImmuneImmune System DiseasesImmune responseIn VitroIndividualInfectionInfiltrationInflammatoryInflammatory ResponseInterleukin-6InvestigationKnowledgeLungMacacaMacaca mulattaMeasuresMediator of activation proteinModelingMonoclonal AntibodiesMyeloid CellsNatural Killer CellsPatientsPharmaceutical PreparationsPlayPneumoniaProteinsProtocols documentationResearchRoleSARS-CoV-2 infectionSamplingSiteSocietiesSymptomsT cell responseT-Cell DepletionT-LymphocyteTestingTherapeuticTimeVaccinesViralVirusanti-viral efficacyantigen-specific T cellscohortcytokineimmunogenicityimmunoregulationinterestmacrophageneutralizing antibodynonhuman primatenovel coronavirusnovel therapeuticsnovel vaccinespreclinical trialpreventremdesivirresponsetherapy design
中文摘要
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英文摘要
Project Summary/Abstract
The novel coronavirus that emerged in late 2019, termed SARS-CoV-2, quickly spread throughout the world
and has, to date, infected millions and killed hundreds of thousands. This virus is shockingly complex in that
the majority of infected individuals show few overt symptoms (though some data suggest they may have
lasting damage nonetheless) but are largely healthy. In contrast, a small fraction of infected individuals exhibit
a range of serious symptoms including pneumonia, acute respiratory distress, clotting disorders, and even
death. The mechanisms that underly mild versus severe symptoms are not fully understood but immune
mechanisms appear to play a role. Thus, we need to understand the roles of particular immune cells in order to
understand the disease and properly treat it. Of particular interest is the role of CD8 T cells (CTL) in disease
outcome. In this project we will use the rhesus macaque model of SARS-CoV-2 infection to assess the
importance of CTL and other CD8+ cells in disease. In aim 1, we will deplete animals of all cells that express
the CD8a molecule, including CTL and NK cells, and assess their ability to clear the virus. In aim 2, we will
target only CTL for depletion and likewise assess their importance. In aim 3, we will use cells in the lab to
assess how CTL interact with virus infected cells. Together, this project will comprehensively assess the
importance of CTL in COVID-19 disease or protection from it.
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会议论文
Pan Coronavirus Genomic Surveillance of a Large NHP Colony
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批准号:10575848
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项目类别:
-
资助金额:$8.75万
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财政年份:2022
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负责人:Nicholas James Maness
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依托单位:
T cell modulation of COVID-19 disease
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批准号:10674085
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项目类别:
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资助金额:$21.88万
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财政年份:2021
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负责人:Nicholas James Maness
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依托单位:
T cell modulation of COVID-19 disease
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批准号:10491340
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项目类别:
-
资助金额:$21.25万
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财政年份:2021
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负责人:Nicholas James Maness
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依托单位:
Reservoir modulation by Nef and anti-nef CTL
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批准号:9927138
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项目类别:
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资助金额:$25.5万
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财政年份:2020
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负责人:Nicholas James Maness
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依托单位:
Reservoir modulation by Nef and anti-nef CTL
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批准号:10261352
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项目类别:
-
资助金额:$21.25万
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财政年份:2020
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负责人:Nicholas James Maness
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依托单位:
Focused characterization of non-canonical T cells against SIV
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批准号:9560521
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项目类别:
-
资助金额:$25.5万
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财政年份:2018
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负责人:Nicholas James Maness
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依托单位:
SIV antisense epitopes as novel markers of latency
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批准号:8846907
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项目类别:
-
资助金额:$25.35万
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财政年份:2015
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负责人:Nicholas James Maness
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依托单位:
海外基金