Grant: Travel Awards - Institute Community Support
York University (Toronto, Ontario)
$1,664.00
Phenotypic characterization of monocytes/macrophages and neutrophils in synovial fluid and blood from PsA patients
EF 2025-26
Résumé
Psoriatic arthritis (PsA) occurs in about 30% of patients with psoriasis. Inflammation within the arthritic joint leads to joint destruction, limitation of function and poor quality of life. Immune cells called macrophages and neutrophils have the capacity to regulate the inflammatory processes that affect progression of arthritis in the joint. Our study will identify these cell populations in joint fluid and blood samples obtained from patients with PsA, study their pro-inflammatory function and associate them with disease severity. This project will provide insights on the potential cellular mechanisms that facilitate inflammation and joint damage in PsA patients, pointing to future novel therapeutic targets.
Programme
Travel Awards - Institute Community Support
Bénéficiaire
Emplacement
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
558599
Name
Oikonomopoulou Katerina
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Travel Awards - Institute Community Support
Projecttitle
Phenotypic characterization of monocytes/macrophages and neutrophils in synovial fluid and blood from PsA patients
Programtype2
Undefined
Orgnameinp2
York University (Toronto, Ontario)
Cihramount2
$1,664
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Ics Travel Awards
Abstract
Psoriatic arthritis (PsA) occurs in about 30% of patients with psoriasis. Inflammation within the arthritic joint leads to joint destruction, limitation of function and poor quality of life. Immune cells called macrophages and neutrophils have the capacity to regulate the inflammatory processes that affect progression of arthritis in the joint. Our study will identify these cell populations in joint fluid and blood samples obtained from patients with PsA, study their pro-inflammatory function and associate them with disease severity. This project will provide insights on the potential cellular mechanisms that facilitate inflammation and joint damage in PsA patients, pointing to future novel therapeutic targets.
Competitiondate
202511
Approvedterm2
1 yr 0 mth
Pinamesdelim
Oikonomopoulou, Katerina
Approvedterm
1 an 0 mois
Cihrcontribution2
III~ $1,664~ $0~