grant

Aging, Sex Bias, and CD8 T Cell Exhaustion in Salivary Gland Inflammation

Organization OKLAHOMA MEDICAL RESEARCH FOUNDATIONLocation OKLAHOMA CITY, UNITED STATESPosted 19 Sept 2025Deadline 18 Sept 2027
NIHUS FederalResearch GrantFY20252 year old2 years of ageAgeAgingAndrogenic AgentsAndrogenic CompoundsAndrogensAntibodiesAntigen-Presenting CellsAntigensAsialiaAttenuatedAutoantibodiesAutoantigensAutoimmune DiseasesAutoimmune StatusAutoimmunityAutologous AntigensBasal Transcription FactorBasal transcription factor genesBiological FunctionBiological ProcessBiopsyBlood SerumBody TissuesC57BL/6 MouseCD8CD8 CellCD8 T cellsCD8 lymphocyteCD8+ T cellCD8+ T-LymphocyteCD8-Positive LymphocytesCD8-Positive T-LymphocytesCD8BCD8B1CD8B1 geneCell BodyCell Communication and SignalingCell SignalingCellsCharacteristicsChromiumChronicComplexComplicationCr elementCytoplasmDetectionDevelopmentDiagnosisDifferentation MarkersDifferentiation AntigensDifferentiation MarkersDiseaseDisorderDisproportionate number of femalesDisproportionate number of menDisproportionate number of womenDisproportionately affects femalesDisproportionately affects womenDisproportionately impacts femalesDisproportionately impacts malesDisproportionately impacts womenDisproportionately in femalesDisproportionately in menDisproportionately in womenDysfunctionEnvironmentEpithelial CellsEpitheliumExhibitsExocrine GlandsExpression SignatureFemaleFlow CytofluorometriesFlow CytofluorometryFlow CytometryFlow MicrofluorimetryFlow MicrofluorometryFormalinFunctional disorderGender BiasGene ExpressionGene Expression ProfileGene TranscriptionGeneral Transcription Factor GeneGeneral Transcription FactorsGenetic PredispositionGenetic Predisposition to DiseaseGenetic SusceptibilityGenetic TranscriptionGenetic propensityGenomicsGerminoblastic SarcomaGerminoblastomaGoalsHumanHyposalivationImmuneImmune DiseasesImmune DisordersImmune DysfunctionImmune System DiseasesImmune System DisorderImmune System DysfunctionImmune System and Related DisordersImmunesImmunologic DiseasesImmunological DiseasesImmunological DysfunctionImmunological System DysfunctionImmunomodulationImmunosuppressionImmunosuppression EffectImmunosuppressive EffectImpairmentInflammationInflammatoryInherited PredispositionInherited SusceptibilityIntracellular Communication and SignalingLYT3Labial Salivary GlandLacrimal deficiencyLifeLinkLiteratureLymphatic cellLymphocyteLymphocyticLymphocytic InfiltrateLymphomaMalignant LymphomaMarker AntigensMiceMice MammalsMinorModern ManMouth DrynessMurineMusNon-Polyadenylated RNANuclearOcular desiccationOvalbuminPD 1PD-1PD1Paraffin EmbeddingPathologyPathway interactionsPhysiopathologyProcessProteinsRNARNA ExpressionRNA Gene ProductsReactionReportingResistanceReticulolymphosarcomaRibonucleic AcidRiskRoleSalivarySalivary Gland DiseasesSalivary GlandsSalivary hypofunctionSelf-AntigensSerumSex BiasSialadenitisSialoadenitisSicca SyndromeSignal PathwaySignal TransductionSignal Transduction SystemsSignalingSjogren's DiseaseSjogren's SyndromeSjogrensSjögren SyndromeStromal CellsSymptomsT cell differentiationT-Cell ActivationT-CellsT-LymphocyteT8 CellsT8 LymphocytesTestingTherapeuticTherapeutic AndrogenTissuesTranscriptionTranscription Factor Proto-OncogeneTranscription factor genesXerostomiaXerostomicaccessory cellactivate T cellsage 2 yearsagedaged 2 yearsaged miceaged mouseaged two yearsagesaptyalismattenuateattenuatesautoimmune antibodyautoimmune conditionautoimmune disorderautoimmunity diseaseautoreactive antibodybiological signal transductioncell typecytokinedevelopmentaldiagnostic criteriadisproportionately affects malesdisproportionately affects mendisproportionately concentrated among mendisproportionately distributed among mendisproportionately higher among mendisproportionately impacts mendisproportionately occurs in mendry eyedry mouthelderly miceexhaustexhaustioneye drynessfemale biasfemale predominancefemale preponderanceflow cytophotometrygene expression patterngene expression signaturegenetic etiologygenetic mechanism of diseasegenetic vulnerabilitygenetically predisposedimmune modulationimmune regulationimmune suppressionimmune suppressive activityimmune suppressive functionimmunogenimmunologic reactivity controlimmunomodulatoryimmunoregulationimmunoregulatoryimmunosuppressive activityimmunosuppressive functionimmunosuppressive responseinnovateinnovationinnovativelymph cellmalemale biasmale predominancemen disproportionately diagnosedmen disproportionately experiencemen experience disproportionate ratesmouse modelmurine modelnew therapeutic approachnew therapeutic interventionnew therapeutic strategiesnew therapy approachesnew treatment approachnew treatment strategynovelnovel therapeutic approachnovel therapeutic interventionnovel therapeutic strategiesnovel therapy approachocular drynessocular signs of drynessocular surface drynessold miceoral drynesspathophysiologypathwaypredominance in femalespredominance in womenpredominantly affecting menprogenitorprogrammed cell death 1programmed cell death protein 1programmed death 1programsresistantsalivary disordersalivary gland disordersalivary gland hypofunctionsalivary gland inflammationscRNA sequencingscRNA-seqself reactive antibodyself-renewself-renewalsexsingle cell RNA-seqsingle cell RNAseqsingle cell expression profilingsingle cell transcriptomic profilingsingle-cell RNA sequencingsle2social rolesystemic autoimmune diseasesystemic autoimmune disordersystemic autoimmunitysystemic lupus erythematosus susceptibility 2tear deficiencythymus derived lymphocytetraffickingtranscription factortranscriptional profiletranscriptional signaturetwo year oldtwo years of agewomen's predominancewomen's preponderancexerodermosteosis
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Full Description

PROJECT SUMMARY
Sjögren’s Disease (SjD) is a systemic autoimmune disorder most frequently targeting exocrine glands and

causing oral and ocular dryness. SjD is characterized by serum antibodies to nuclear and cytoplasmic

antigens and salivary gland inflammation (sialoadenitis), which is associated with an increased risk of

lymphoma. For unknown reasons, SjD disproportionately affects females and is typically diagnosed in the 5th-

6th decade of life. Thus, female sex and aging are intricately linked with immune dysfunction and autoimmunity

in SjD. The long-term goal of this project is to understand the age- and sex-related immune mechanisms

involved in the salivary gland pathology of SjD. The proposed studies will utilize male and female mice that

spontaneously develop the salient characteristics of SjD and mimic the age- and sex-bias of the disease.

While both males and females develop systemic autoimmunity, only the females progress to severe

sialoadenitis. We will use a conceptually innovative approach by investigating the immunoregulatory

mechanisms that protect males from severe sialoadenitis. Aim 1 will investigate whether the aged male

salivary gland microenvironment harbors immunosuppressive signals that inhibit progressive inflammation.

We will characterize gene expression changes in immune, epithelial, and stromal compartments using single-

cell transcriptomic profiling of male and female salivary glands at key aging milestones. Recent literature

suggests a prominent role for CD8 T cells in the glandular pathology of SjD. Aim 2 will examine the

differentiation trajectory of CD8 T cells targeting salivary gland antigens in male and female mice. We will

leverage a novel mouse model expressing ovalbumin as a surrogate self-antigen in the salivary glands to

track antigen-specific CD8 T cell activation. Our findings will inform the development of innovative therapeutic

strategies aimed at local immune modulation to alleviate salivary gland pathology in SjD.

Grant Number: 1R21DE034962-01A1
NIH Institute/Center: NIH

Principal Investigator: HARINI BAGAVANT

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