Core C: Humoral and Serological Core
Core C: Humoral and Serological Core
批准号:
10425266
负责人:
Scott Eric Hensley
金额:
$19.57万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-06-08 至 2024-05-31
关键词:
AddressAdultAffectAffinityAntibodiesAntibody ResponseB-LymphocytesB-cell receptor repertoire sequencingBindingBiological AssayCancer PatientChildhood Acute Lymphocytic LeukemiaClinicalComplexCytomegalovirusDataData SetDrug TargetingEnzyme-Linked Immunosorbent AssayExposure toFlu virusGlobal ChangeGoalsHealthHepatitis B VirusHepatitis C AntibodiesHepatitis C virusHumanHuman Herpesvirus 4ImmuneImmune responseImmunityImmunoglobulin GImmunologicsImmunomodulatorsImmunotherapyIndividualInfluenzaInfluenza vaccinationLifeMeasurementMeasuresMemoryMemory B-LymphocytePD-1 blockadePatientsPeptidesSamplingSerologySerology testSerumServicesSpecificityStandardizationTechniquesTechnologyTestingThermometersVaccinesViralViral AntibodiesViral AntigensVirusanti-PD1 therapyanti-hepatitis Banti-influenzabasechronic infectionexposed human populationfluinfluenzavirusinnovationmemory recallprogrammed cell death protein 1response
中文摘要
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英文摘要
Project Summary
A major goal of this U19 is to determine how PD-1 blockade affects human antibody responses against
different viral antigens. Core C will fully interrogate serum antibody responses against a range of different
viruses from donors undergoing PD-1 therapy in Projects 1 and 2. The Core will standardize assays, complete
assays, and provide computational support for the analyses of complex serological datasets. We will offer
standardized ELISA-based services that quantify antibodies specific for 5 viruses that are relevant for Projects
1 and 2. We will also assess quality of antibody responses through ELISAs that measure relative affinities and
isotype diversity. It is possible that PD-1 blockade affects antiviral antibody responses in more subtle or global
ways. To address this, we will complete serological screens to examine how PD-1 blockade affects antibody
responses to a large fraction of known human viruses. For this, we will use a new array-based assay, termed
‘Viroscan’, that measures antibody binding to >400,000 non-redundant viral peptides. We will also offer
services that intensively analyze antibody responses against a single virus (influenza). All humans are
exposed to influenza virus in childhood and all adult encounters with influenza involve both the recall of
memory B cells and the stimulation of de novo B cell responses. Our influenza virus antigenic analyses will
allow us to determine if PD-1 blockade differentially regulates de novo versus memory antibody responses.
Together, these standardized services will allow for the complete antigenic characterization of serum samples
for Projects 1 and 2.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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财政年份:2014
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财政年份:2014
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依托单位:
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批准号:8756454
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财政年份:2014
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依托单位:
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批准号:8099226
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项目类别:
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资助金额:$16.2万
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财政年份:2011
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负责人:Scott Eric Hensley
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依托单位:
Elucidation of mechanisms that contribute to antigenic drift of influenza viruses
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批准号:8255436
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项目类别:
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财政年份:2011
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依托单位:
Core C: Humoral and Serological Core
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批准号:10180873
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项目类别:
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依托单位:
Core C: Humoral and Serological Core
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项目类别:
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资助金额:$19.09万
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依托单位:
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项目类别:
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资助金额:$28.66万
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财政年份:--
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负责人:Scott Eric Hensley
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依托单位:
海外基金