grant

Serum components to support corneal health

Organization UNIVERSITY OF CALIFORNIA, SAN FRANCISCOLocation SAN FRANCISCO, UNITED STATESPosted 1 Jan 2025Deadline 31 Dec 2026
NIHUS FederalResearch GrantFY2025AddressAffectAssayAutologousBioassayBiochemicalBiologic FactorBiological AssayBiological FactorsBloodBlood PlasmaBlood Reticuloendothelial SystemBlood SerumBlood TestsCell BodyCell Communication and SignalingCell SignalingCellsChemical FractionationChemical InjuryClinicalClinical ResearchClinical StudyComplexConjunctivitisCorneaCorneal InjuryDefectDiseaseDisorderDry Eye SyndromesDry eye diseaseElementsEpitheliumExposure toExpression SignatureFRACNFormulationFractionationFractionation RadiotherapyGene Expression ProfileGene TranscriptionGenetic TranscriptionGrowth AgentsGrowth FactorGrowth SubstancesHealthHematologic TestsHematological TestsHematology TestingHumanIn vivo analysisIndividualIntracellular Communication and SignalingInvestigationKeratoconjunctivitisKeratoconjunctivitis SiccaKeratopathyLipidsLiquid substanceMass Photometry/Spectrum AnalysisMass SpectrometryMass SpectroscopyMass SpectrumMass Spectrum AnalysesMass Spectrum AnalysisMediatingMiceMice MammalsModern ManMolecularMurineMusOphthalmologyPathway interactionsPatientsPlasmaPlasma SerumPreparationProcessProgenitor CellsPropertyProteinsProteins Growth FactorsRNA ExpressionReceptor ProteinRecombinantsRecurrenceRecurrentReticuloendothelial System, Serum, PlasmaSerumSicca SyndromeSignal TransductionSignal Transduction SystemsSignalingSjogren's DiseaseSjogren's SyndromeSjogrensSjögren SyndromeSymptomsSyndromeTechniquesTestingTherapeutic EffectTimeTranscriptionVitaminsWound Repairbiological signal transductionblood productcell typechemical traumaclinical applicabilityclinical applicationcornealcorneal repaircorneal woundcostcrosslinkdisease modeldisorder modelfluidgene expression patterngene expression signatureimprovedin vitro Assayin vivoin vivo evaluationin vivo testinginsightlimballiquidmouse modelmurine modelnovelocular surfaceocular surface diseaseocular surface disorderpathwaypreparationsreceptorscRNA sequencingscRNA-seqsingle cell RNA-seqsingle cell RNAseqsingle cell expression profilingsingle cell transcriptomic profilingsingle-cell RNA sequencingstem cellssynergismtheoriestherapeutic targettranscriptional profiletranscriptional signaturewound healingwound recoverywound resolutionxerodermosteosis
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Full Description

PROJECT SUMMARY
For almost 50 years, blood-based therapies, such as autologous serum tears (ASTs), have been used in clinical

ophthalmology to treat diverse ocular surface disorders including Sjogren's syndrome-related dry eye disease,

persistent epithelial defects, chemical injury, recurrent erosion syndrome, superior limbic keratoconjunctivitis,

neurotrophic keratopathy, limbal stem cell disease, cicatrizing conjunctivitis, and post-corneal cross-linking haze.

It is theorized that serum has components that either replace those missing endogenously or modulate pathways

to restore healthy function. However, to date, there has been no detailed molecular characterization of serum

tears in the context of ocular surface disease. The poorly defined mechanism of serum tears in treating ocular

surface disease leads to two important challenges in their clinical application: (1) the lack of a standard

concentration for preparation, and (2) the inconvenient and costly process of obtaining ASTs. Thus, despite

many clinical studies that demonstrate the ability of serum tears to improve both objective signs and subjective

symptoms of ocular surface disorders, formulation and accessibility issues have limited its more widespread use.

Our overall objective is to define the combinations of serum components (growth factors, signaling lipids,

vitamins, etc.) that support corneal repair. We hypothesize that the effects of serum tears are due a simple

combination of bioactive factors, some of which remain to be characterized, or the result of synergistic actions

of serum components. Our studies seek to determine bioactive serum tear components and define synergism

between components, and characterize the in vivo effects of blood-based tears in an ocular surface disease

model. We anticipate this project will yield both translational insight to the clinical use of serum tears, and likely

improve current formulation and accessibility issues which may allow for more widespread use. Furthermore,

the identification and characterization of bioactive serum tear components is expected to reveal potential

therapeutic targets for further exploration.

Grant Number: 1R21EY035829-01A1
NIH Institute/Center: NIH

Principal Investigator: Matilda Chan

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