Exploring the biology of persistent type 2 airway niches in asthma
Project Number5P01HL107202-07
Contact PI/Project LeaderFAHY, JOHN V
Awardee OrganizationUNIVERSITY OF CALIFORNIA, SAN FRANCISCO
Description
Abstract Text
Summary / Abstract
This is a renewal application for a PPG that focuses on mechanisms of persistence of type 2 inflammation in
asthma. The central theme of our PPG is that the focal nature of type 2 inflammation that occurs in asthma
reflects the development of persistent “type 2 airway niches” that are characterized by epithelial cell and immune
cell reprogramming and mucus plug formation. Normal homeostatic responses to aeroallergens and other
inhaled insults include communications between epithelial cells and innate cells to recruit adaptive cells that limit
type 2 immune responses and restore airway function. When these repair mechanisms fail the normal airway
immune program is replaced by adaptive responses that favor persistence of airway type 2 inflammation and
formation of mucus plugs. This persistent and “ultra high” type 2 inflammation occurs in focal regions of the
asthma lung, as evidenced by our recent finding of focal and persistent eosinophilic mucus plugs in lung images
from patients with asthma. Our PPG will explore the biology of these focal type 2 airway niches in three
overarching aims. AIM 1 will determine how innate and adaptive immune cells in the persistent airway type 2
niche are reprogrammed to sustain inflammation. AIM 2 will determine how airway epithelial cells are
reprogrammed in type 2 niches to sustain inflammation. AIM 3 will determine how epithelial cells and eosinophils
sustain mucus gel pathology in type 2 airway niches. Our PPG comprises three projects led by multidisciplinary
teams of clinical scientists, immunologists and cell biologists. The projects are supported by three cores -
administration, human subjects, and biospecimens and bioinformatics. Our PPG proposes innovative concepts
for the pathogenesis of type 2-high asthma and it will deploy powerful and cutting edge technologies in the
experimental approaches that address our program aims. We are united in our ambition to aim for discoveries
that have the potential to lead to curative treatments for type 2-high asthma.
Public Health Relevance Statement
Project Narrative
This program project grant renews a highly-successful collaboration between leading clinical scientists,
immunologists, and cell biologists who seek to uncover the key tissue-immune checkpoints that lead to persistent
airway type 2 inflammation and mucus plug formation in asthma. Here we use novel experimental approaches
including image guided bronchoscopy and high-dimensional single cell analytics to decode the regulatory
networks that sustain severe disease. Our research focuses on discoveries that will directly impact the health of
patients for whom current treatments have failed.
NIH Spending Category
No NIH Spending Category available.
Project Terms
ATAC-seqAddressAllergic inflammationAnionsAsthmaBasophilsBehaviorBioinformaticsBiologyBronchoscopyCRISPR/Cas technologyCell Differentiation processCell Fate ControlCellsCellular biologyChestClinicalCollaborationsCommunicationCytometryDataDevelopmentDiseaseEffector CellEpidemiologistEpigenetic ProcessEpithelialEpithelial CellsEpitheliumFacultyGelGene ExpressionGenesGeneticGoblet CellsHealthHumanImmuneImmune responseImmunityImmunologistInflammationInflammatory ResponseInhalationInjuryInterleukin-13Interleukin-5InterventionInvestigationLeadLigandsLungLung CAT ScanLymphocyteMediatingMessenger RNAMethodsMethylationMicroRNAsMucinsMucous body substanceMusMyelogenousNasal PolypsNatureOtolaryngologistOxidantsPathogenesisPathologicPathologyPatient imagingPatientsPlug-inProductionProgram Research Project GrantsPublicationsRNA analysisResearchResearch PersonnelRoleSamplingScientistSecretory CellSeminalSignal TransductionSourceSystemT-LymphocyteTechnologyTestingTh2 CellsTissuesTrainingUnited States National Academy of SciencesWorkX-Ray Computed Tomographyairborne allergenairway epitheliumairway inflammationasthmatic patientbiobankcrosslinking and immunoprecipitation sequencingcurative treatmentscytokineeosinophileosinophil peroxidaseepithelial injuryhigh dimensionalityhuman subjectimage guidedimmune checkpointinnovationlung imagingmast cellmembermultidisciplinarynovelnovel therapeuticsprogramsradiologistreceptorreceptor functionrecruitrepairedresponsesensorsuccesstranscription factortranscriptome sequencingtranscriptomics
No Sub Projects information available for 5P01HL107202-07
Publications
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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