Canada Spends Logo

Explore our Budget 2026 analysis

Grant: Collaborative Health Research Projects

Université de Montréal

$255,159.00

Targeting the interleukin-1 receptor for treating ischemic eye diseases

FY 2017-18

Summary
Ischemic retinopathies are diseases caused by obstruction of blood vessels that damage the retina. The retina is the part ofthe eye that possesses cells which sense light, as well as blood vessels that bring nutrients to these cells. Oxidant stressand inflammation are early intertwined common features of ischemic retinopathies, such as those associated withprematurity and diabetes, the two most common retinopathies, respectively of childhood and adults under the age of 65.Inflammation elicits abnormalities in these vessels causing leakage of intravascular fluids and obliteration of capillaries thatcause deterioration of the retina resulting in vision loss. No cures exist presently for these diseases. Treatments typicallyaim to destroy abnormal blood vessels using laser photocoagulation. Attempts to use steroids and agents that arrest bloodvessel growth (so called anti-VEGF therapy) have shown limited success, in part because they either exert modest antiinflammatoryeffects or only tackle the late stage edema and pre-retinal neovascularization, without addressing thepredisposing inflammation. The proposed research tackles the inflammatory aspect of ischemic retinopathy by targeting theinterleukin-1 receptor (IL-1R) using novel compounds that interfere with the inflammatory process, prevent vessel destructionand lead to normalization of vessel density, without compromising local immune surveillance and cytoprotection. Ourpromising preliminary results with new IL-1R modulators merits further study to enhance their potential as novel therapeuticsto treat these major vision-robbing diseases.
Program
Collaborative Health Research Projects
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
493638-2016
Name nom
Lubell, William
Department département
Chimie
Organization id
63
Institution établissement
Université de Montréal
Province en
Québec
Province fr
Québec
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2017
Competition year année de concours
2016
Award amount
255159
Program id
CHRPJ
Program name en
Collaborative Health Research Projects
Program name fr
Projets de recherche concertée sur la santé
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
360
Committee name en
Collaborative Health Research Projects Selection Panel
Committee name fr
Comité de sélection de projets de recherche concertée sur la santé
Area of application code
9999
Area of application group en
Not available
Area of application group fr
Non disponible
Area of application en
Not available
Area of application fr
Non disponible
Research subject code
9999
Research subject group en
Not available
Research subject group fr
Non disponible
Research subject en
Not available
Research subject fr
Non disponible
Partie
2 & 3
Nb partie
3
Application title
Targeting the interleukin-1 receptor for treating ischemic eye diseases
Keyword
NSERC
Application summary
Ischemic retinopathies are diseases caused by obstruction of blood vessels that damage the retina. The retina is the part ofthe eye that possesses cells which sense light, as well as blood vessels that bring nutrients to these cells. Oxidant stressand inflammation are early intertwined common features of ischemic retinopathies, such as those associated withprematurity and diabetes, the two most common retinopathies, respectively of childhood and adults under the age of 65.Inflammation elicits abnormalities in these vessels causing leakage of intravascular fluids and obliteration of capillaries thatcause deterioration of the retina resulting in vision loss. No cures exist presently for these diseases. Treatments typicallyaim to destroy abnormal blood vessels using laser photocoagulation. Attempts to use steroids and agents that arrest bloodvessel growth (so called anti-VEGF therapy) have shown limited success, in part because they either exert modest antiinflammatoryeffects or only tackle the late stage edema and pre-retinal neovascularization, without addressing thepredisposing inflammation. The proposed research tackles the inflammatory aspect of ischemic retinopathy by targeting theinterleukin-1 receptor (IL-1R) using novel compounds that interfere with the inflammatory process, prevent vessel destructionand lead to normalization of vessel density, without compromising local immune surveillance and cytoprotection. Ourpromising preliminary results with new IL-1R modulators merits further study to enhance their potential as novel therapeuticsto treat these major vision-robbing diseases.