grant

Systems Serology Core

Organization UNIVERSITY OF MARYLAND BALTIMORELocation BALTIMORE, UNITED STATESPosted 12 Jul 2021Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY20250-4 weeks old21+ years oldAddressAdultAdult HumanAffectAntibodiesAntibody ResponseAreaAssayAutologousBenchmarkingBest Practice AnalysisBioassayBiological AssayBiophysicsBirthCell BodyCellsCollectionDataDevelopmentDimensionsEnsureEnvironmentFingerprintGenerationsGestationGlycoengineeringGoalsHumanHuman ResourcesHumoral ImmunitiesImmuneImmune responseImmune systemImmunesImmunityImmunochemical ImmunologicImmunologicImmunologicalImmunologicallyImmunologicsInfantInfant HealthInfectionInfrastructureInterventionInvestigationKnowledgeLaboratoriesLeadershipLifeManpowerMaternal ImmunityMaternal antibodyMaternally-Acquired ImmunityModern ManMonitorNatureNeonatalNewborn InfantNewbornsParturitionPregnancyProtocolProtocols documentationQualifyingReagentResearchResearch ResourcesResourcesRoleRunningSamplingSerologyStandardizationSystemTechnical ExpertiseTechnologyTherapeuticTrainingVaccinesWorkadulthoodantibody assayantibody based testantibody testantibody-based immunitybenchmarkbiophysical foundationbiophysical principlesbiophysical sciencesconditioningdevelopmentalhigh standardhost responseimmune response to vaccinationimmune response to vaccinesimmune system responseimmunoresponseimprovedin uterolab experiencelab traininglaboratory experiencelaboratory trainingmaternal immunizationmaternal vaccinationneonatal immunityneonatenew technologynewborn childnewborn childrennext generationnovelnovel technologiespersonnelprogramsresponsesocial rolesuccesssynergismtechnical skillstechnology platformtechnology systemtoolvaccine associated immune responsevaccine immune responsevaccine immunogenicityvaccine induced immune response
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Full Description

CORE 1 – SYSTEMS SEROLOGY CORE – ABSTRACT
Accumulating data points to dramatic immunologic changes during pregnancy and early life. However, how these

immune perturbations alter the immune response to vaccination or to infection have yet to be fully defined. Under

Core 1, in depth comprehensive characterization will be performed on the humoral immune response to improve

our understanding of the mechanisms by which the immune system changes throughout pregnancy, how these

changes affect responses to vaccines and how infants benefit from maternal immunity and in turn respond to

vaccines. Specifically, Core 1 will exploit and evolve Systems Serology to broadly and deeply probe the nature

of the humoral immune response in a sample sparing manner, via the development of multiplexed-antibody

profiling approaches. Additionally Core 1 will develop lower-throughput functional assays to probe the interaction

between antibodies and host-innate immune cells, in a fully autologous fashion, to define the overall impact of

altered antibody and cellular state in pregnancy and early life. Thus Core 1 will deeply interrogate and define

changes in humoral immunity throughout pregnancy, at birth, and throughout early infant life. The Core leader

will provide all the expertise, infrastructure, reagents, personnel, and training, to ensure the efficient and

successful analysis and deployment of this technology under Projects 1 & 2, as well as support in generating

data for Projects 2 & 4. Thus the main role of this Core is to provide the leadership and the technical expertise

to ensure that antibody assays are run in a standard fashion, that novel technologies evolve from this Core to

support the needs of the overall Consortium, and that the Consortium is kept abreast of the latest developments

in assessing antibody responses.

Grant Number: 5U19AI145825-05
NIH Institute/Center: NIH

Principal Investigator: Galit Alter

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