Staphylococcus aureus interference with IsdB vaccination
Staphylococcus aureus interference with IsdB vaccination
批准号:
10020319
负责人:
George Y Liu
金额:
$54.18万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-18 至 2024-08-31
关键词:
AddressAffectAgeAntibiotic ResistanceAntibodiesAntibody DiversityAntibody ResponseB-Cell ActivationB-LymphocytesBLT miceBacterial VaccinesBindingCharacteristicsClinical TrialsDataEpitopesExposure toFailureFrequenciesGenerationsGeneticGenus staphylococcusHumanImmune responseImmunityImmunizationInfectionInfectious Skin DiseasesInterleukin-10IronLaboratory AnimalsLeadLifeMediatingModificationMusPharmacologic SubstancePublic HealthResearch PersonnelResourcesRodentSpecificityStaphylococcal InfectionsStaphylococcal VaccinesStaphylococcus aureusStaphylococcus aureus infectionSurfaceTestingTimeVaccinatedVaccinationVaccinesViraladoptive B cell transferclinically relevantcombatexperienceexperimental studyexposed human populationhuman pathogenhumanized mouseinfection ratemethicillin resistant Staphylococcus aureusmouse modelnovelnovel strategiesphase III trialresponsesuccessvaccine developmentvaccine efficacyvaccine evaluationvaccine responsevaccine trial
中文摘要
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英文摘要
ABSTRACT
Staphylococcus aureus is a leading cause of infection worldwide and a major driver of antibiotic resistance.
Although many staphylococcal vaccines have been developed, all vaccines tested to date in human trials have
failed for unclear reasons. Unlike humans who are infected or colonized with S. aureus at an early age,
laboratory animals are rarely exposed to the human pathogen. Therefore, we queried if prior S. aureus
exposure, in the form of infection, modifies protective immunity conferred by IsdB vaccination. Strikingly, prior
staphylococcal infection in mice interferes with the induction of anti-staphylococcal immunity by IsdB
vaccination. The mechanism appears to be driven by IL-10 and S. aureus-experienced B cells. These findings
led us to hypothesize that S. aureus infection induces an ineffective B cell response associated with IL-10 that
is preferentially recalled when subsequent IsdB vaccine is administered (original antigenic sin). To address
our hypothesis, in Aim 1, we will determine how S. aureus- activated B cells and IL-10 modulate the host
immune response to IsdB vaccine and nullify anti-staphylococcal protection. In Aim 2, we will determine what
modifications to the IsdB-specific antibodies, induced by prior S. aureus exposure, make the antibodies non-
protective. In Aim 3, we will determine the broader clinical relevance of our findings by testing if vaccine
interference occurs in humanized BLT mice and in various clinically relevant settings.
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Staphylococcus aureus interference with IsdB vaccination
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Staphylococcus aureus interference with IsdB vaccination
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Staphylococcus aureus interference with IsdB vaccination
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