grant

Vaccines and antibodies for arenaviruses

Organization VANDERBILT UNIVERSITY MEDICAL CENTERLocation NASHVILLE, UNITED STATESPosted 20 Aug 2024Deadline 31 Jul 2027
NIHUS FederalResearch GrantFY2024Active immunityAd vectorAdenoviral VectorAdenovirus VectorAntibodiesAntigenic DeterminantsAreaArenaviridaeArenavirusArenavirus groupArgentine hemorrhagic fever virusArgentinian Hemorrhagic Fever VirusAttenuatedBBC1BCL2-Interacting Killer GeneBIKBIK geneBIP1BP4Bik/Nbk GeneBinding DeterminantsBlood VesselsBunyavirusClinicalClinical Treatment MoabCollaborationsCombined Modality TherapyDNA deliveryDataDevelopmentDiseaseDisorderEpitopesExtravasationFamilyFamily PicornaviridaeGenesGenetic AlterationGenetic ChangeGenetic defectHalf-LifeHantavirusHu-mABsHumanImmuneImmune responseImmunesImmunityImmunocompromisedImmunocompromised HostImmunocompromised PatientImmunological responseImmunosuppressed HostInfectionInjectionsJuninJunin virusLCM VirusesLCMVLassa fever virusLassa virusLeadLeakageLymphocytic choriomeningitis virusM mulattaM. mulattaMacacaMacaca mulattaMacaqueMedicalMeningitisMessenger RNAModelingModern ManMonoclonal AntibodiesMultimodal TherapyMultimodal TreatmentMutationNBKOrthobunyavirusPassive ImmunityPathogenesisPathogenicityPb elementPicornaviridaePicornavirusesPreparednessProteinsReadinessReagentResistanceResponse GeneralizationRhesus MacaqueRhesus MonkeyRoleSpillageSyndromeT cell responseT-CellsT-LymphocyteTechnologyTherapeuticTherapeutic antibodiesVaccination acquired immunityVaccination induced immunityVaccine DesignVaccinesViral DiseasesViral Hemorrhagic FeversVirusVirus DiseasesWorkadeno vectoradenovectorattenuateattenuatesclinical developmentcombination therapycombined modality treatmentcombined treatmentdata managementdeliver DNAdesigndesigningdevelopmentalevaluate vaccinesexperiencegenome mutationheavy metal Pbheavy metal leadhemorrhagic feverhost responsehumAbshuman mAbshuman monoclonal antibodieshuman monoclonalsimmune system responseimmunogenicityimmunoresponseimmunosuppressed patientindustrial partnershipindustry partnerindustry partnershipinsightlead candidatemAbsmRNAmanufacturing capabilitiesmanufacturing capacitymedical countermeasuremonoclonal Absmulti-modal therapymulti-modal treatmentneutralizing mAbneutralizing monoclonal antibodiesnon-human primatenonhuman primatepandemic concernpandemic disease preparednesspandemic pathogenpandemic planningpandemic potentialpandemic preparednesspandemic readinesspandemic riskpandemic threatpathogenpathogenic virusplasmid vaccinepre-clinicalpre-clinical developmentpreclinicalpreclinical developmentprophylacticprotective efficacyprototyperesistantsocial rolesynergismtechnology platformtechnology systemtherapeutic agent developmenttherapeutic developmentthymus derived lymphocytevaccine acquired immunityvaccine associated immunityvaccine candidatevaccine evaluationvaccine platformvaccine screeningvaccine strategyvaccine testingvaccine-induced immunityvaccine-induced protectionvascularvectorvector vaccineviral infectionviral pathogenvirus infectionvirus pathogenvirus-induced disease
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Full Description

PROJECT SUMMARY - RP5
Arenaviruses, a family of viruses with pandemic potential, can cause hemorrhagic fever, meningitis, and other

clinical syndromes. These viruses include highly pathogenic strains such as Lassa virus (LASV) and Junín

virus (JUNV), as well as less pathogenic strains like lymphocytic choriomeningitis virus (LCMV). In this project,

we aim to focus on two major areas, active immunity induced by experimental vaccines and passive immunity

conferred by injection with human monoclonal antibodies. The later studies will include the study of extended

half-life protective antibodies bearing Fc mutations that cause ≥90-day half-life profiles in humans and thus

enable a vaccine-like prophylactic profile of a year or more. First, in studies in Aim 1, we will compare leading

vaccine platform technologies and define immune correlates of protection for LCMV in nonhuman primate

models of infection (macaques) as a virus prototype. Understanding the principles of immunity to this prototype

virus will allow us then to pivot and use those mechanistic insights to design and test vaccines for other

arenaviruses. This work will allow us to fully explore replicating attenuated LCMV vectors as a strategy for

developing candidate arenavirus vaccines. We also will explore the hypothesis that both antibodies and T cell

responses contribute to vaccine -induced protection against LCMV. Next, in studies in Aim 2, we will focus on

deploying optimal vaccine strategies for other arenaviruses of pandemic concerns, LASV and JUNV. Lastly, in

work in Aim 3, we will identify and characterize fully human neutralizing monoclonal antibodies and their

epitope targets, with initial work in LCMV antibody discovery providing a platform for further work on other

medically important arenaviruses. This project will be synergistic with other projects in the BP4 center focusing

on picornavirus and hantavirus vaccines and with the BP4 human monoclonal antibody projects to develop

candidate arenavirus, picornavirus, and hantavirus medical countermeasures.

Grant Number: 1U19AI181979-01
NIH Institute/Center: NIH

Principal Investigator: ROBERT CARNAHAN

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