grant

Influence of Exposure to a Mixture of PFAS and Metals on the developing immune system

Organization UNIVERSITY OF CALIFORNIA BERKELEYLocation BERKELEY, UNITED STATESPosted 1 Apr 1997Deadline 30 Jun 2027
NIHUS FederalResearch GrantFY2025(TNF)-α0-11 years old1st trimester21+ years old7 year old7 years of ageAb responseAccountingAddressAdultAdult HumanAffectAnimal ModelAnimal Models and Related StudiesAntibody FormationAntibody ProductionAntibody ResponseAntibody titer measurementArsenicAttenuatedB cell differentiation factorB cell stimulating factor 2B pertussis infectionB-Cell Differentiation FactorB-Cell Differentiation Factor-2B-Cell Stimulatory Factor-2B. pertussis infectionBCDFBSF-2BSF2Biological MarkersBirthBloodBlood PlasmaBlood Reticuloendothelial SystemBlood leukocyteBordetella pertussis infectionBostonCSIFCSIF-10CachectinCell Proliferative ActivityCellular Proliferation RateChemical ExposureChemicalsChildChild YouthChildhoodChildren (0-21)Cohort StudiesComplexConcurrent StudiesCord BloodCytokine Synthesis Inhibitory FactorDNA MethylationDataData ScienceDevelopmentDiphtheriaDiphtheria ToxoidDiphtheria VaccineDiseaseDisorderDoseEarly Placental PhaseEnvironmentEnvironmental ExposureEnvironmental PollutantsEpidemic ParotitisEpidemiologic ResearchEpidemiologic StudiesEpidemiological StudiesEpidemiology ResearchExposure toFirst Pregnancy TrimesterFirst TrimesterGenesGerman MeaslesGestationGoalsGuidelinesHAZMATHPGFHazardous MaterialsHazardous SubstancesHealthHepatocyte-Stimulating FactorHg elementHumanHybridoma Growth FactorIFN-beta 2IFNB2IL-10IL-13IL-6IL10IL10AIL13IL6 ProteinImmuneImmune MarkersImmune responseImmune systemImmunesImmunityImmunizationImmunologic MarkersImmunomodulationIndividualInterleukin 10 PrecursorInterleukin-10Interleukin-13Interleukin-6JointsKnowledgeLeadLeukocytesLeukocytes Reticuloendothelial SystemLifeLife CycleLife Cycle StagesMGI-2MMR VaccineMacrophage-Derived TNFMarrow leukocyteMeaslesMeasles-Mumps-Rubella VaccineMeasuresMediatingMediatorMercuryMetal exposureMetalsMethodologyMethodsMethylationMitotic IndexModern ManMonocyte-Derived TNFMothersMumpsMyeloid Differentiation-Inducing ProteinPFASParturitionPathway interactionsPb elementPertussisPlasmaPlasma SerumPlasmacytoma Growth FactorPoisonPoly-fluoroalkyl substancesPopulationPredispositionPregnancyPreventative strategyPreventionPrevention strategyPreventive strategyProliferation IndexPublic HealthReportingResearchResearch SpecimenReticuloendothelial System, Serum, PlasmaRiskRisk AssessmentRubellaRubella VaccineRubella virus vaccineRubeolaS-Phase FractionSamplingSchool-Age PopulationSerologySpecimenSusceptibilitySystems DevelopmentTNFTNF ATNF AlphaTNF geneTNF-αTNFATNFαTestingTetanusTetanus VaccineToxic ChemicalToxic SubstanceToxicologyTumor Necrosis FactorTumor Necrosis Factor-alphaUmbilical Cord BloodVaccinationVaccination acquired immunityVaccination induced immunityVaccinesWater PollutantsWhite Blood CellsWhite CellWhooping Coughadulthoodage 7 yearsantibody biosynthesisantibody titeringarsenicsattenuateattenuatesbio-markersbiologic markerbiomarkerchemical reductionclinical relevanceclinically relevantclostridial tetanuscohortcytokinedevelopmentalearly childhoodearly life exposureenvironmental contaminantepidemic parotiditisepidemiologic investigationepidemiology studyepigenomeexposed human populationexposed in uteroexposure to metalfetal cord bloodfetal exposurefetal substance exposuregenome scalegenome-widegenomewidehaz matheavy metal Pbheavy metal leadhost responsehuman exposureimmune modulationimmune regulationimmune system responseimmune-based biomarkersimmunoglobulin biosynthesisimmunologic reactivity controlimmunological biomarkersimmunological markersimmunomodulatoryimmunoregulationimmunoregulatoryimmunoresponseimmunotoxicityin utero exposureinfected with B pertussisinfected with B. pertussisinfected with Burkholderia pertussisinterferon beta 2intra-uterine environmental exposureintrauterine environmental exposurekidslife courselymphocyte proliferationmodel of animalmorbillinoveloffspringpathwaypediatricperfluorinated alkyl substancesperfluoroalkyl substancesperfluoroalkylated substancespolyfluorinated alkyl substancespolyfluoroalkyl substancespostnatalprenatalprenatal exposureprenatal influenceprenatal substance exposureprenatally exposedprospectiverecruitresponserubella antibodiesschool ageseven year oldseven years of agetoxic compoundtoxic reaction in immunologyunbornvaccine acquired immunityvaccine associated immunityvaccine-induced immunityvaccine-induced protectionwater contaminantwhite blood cellwhite blood corpuscleyoungster
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Full Description

PROJECT 2: SUMMARY/ABSTRACT
Early-life exposures, both prenatally and in early childhood, can lead to lasting consequences in the development

of health and disease throughout the life-course. Two major classes of ubiquitous chemicals detected almost

universally across human populations are metals and synthetic per- and polyfluoroalkyl substances (PFAS).

Metals and metalloids, such as lead and arsenic, are known hazardous substances and prenatal exposure has

been shown to modulate the developing immune system. Similarly, exposure to PFAS consistently has been

associated with decreased immune response to important childhood immunizations like the tetanus and

diphtheria vaccines. However, our understanding of the combined impact of these two classes of chemicals on

the developing immune system and immune response remains limited. While childhood immunization remains

a cornerstone for public health prevention our understanding on how early-life chemical exposures affect immune

system development and response remains extremely limited. Even more limited is our understanding of the

joint contribution of multiple chemical exposures in early life on the immune system. Current risk assessments

for these compounds are performed with adult endpoints and estimates of exposure to a single chemical. We

propose to comprehensively and systematically investigate the influence of prenatal and early-life exposure to a

mixture of metals and PFAS on the developing immune system and their influence on vaccine-induced immunity.

We are leveraging specimens from Project Viva, a prospective birth cohort recruited in Boston, MA to 1)

Determine if a prenatal mixture of first trimester metals and PFAS are individually and jointly associated as a

mixture with cord blood cytokines and lymphocyte proliferation at birth; 2) Quantify the extent to which a prenatal

metal/PFAS mixture is associated with Tetanus, Diphtheria and Pertussis (TDAP) and Measles, Mumps, and

Rubella (MMR) vaccine titers in mid-childhood (~7 years of age) and evaluate the extent to which postnatal

childhood metal and PFAS exposure contributes to this relationship; and 3) Test if DNA methylation signatures

at birth measured in leukocytes mediate associations between prenatal chemical exposure and reduced TDAP

and MMR vaccine antibody response in childhood. In this project we will test longitudinal associations in a large

cohort of mother-child pairs with detailed confounder information and existing high-quality data and samples. We

will implement novel statistical methodology to test different prenatal and postnatal environmental mixtures to

comprehensively quantify the impact of chemical exposures on the developing immune system and vaccine-

induced immunity. This project will provide critical knowledge on the developmental immunotoxicity of PFAS and

metals, individually and as a mixture, at environmentally relevant concentrations for the U.S. population. The

immune parameters of this research are clinically relevant and will help inform risk assessments for individuals

as well as public health guidelines with the goal of protecting children.

Grant Number: 4P42ES004705-37
NIH Institute/Center: NIH

Principal Investigator: Andres Cardenas

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