Grant: DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
Ottawa Hospital Research Institute
$120,000.00
Harnessing IL-33 and Checkpoint Blockade to Boost Adaptive Immunity in Ovarian Cancer
FY 2025-26
Summary
Survival rates for ovarian cancer have remained largely unchanged for decades, partly because current treatments are not effective enough to cure patients. One promising strategy is immunotherapy, which strengthens the body's own immune system to fight cancer. While this approach has been very successful in other cancer types, it has not worked well for ovarian cancer. Our research aims to develop more effective immunotherapies for ovarian cancer using clinically relevant mouse models that closely mimic human disease. We believe that by gaining a deeper understanding of how the immune system interacts with ovarian tumors, we can design better treatments for patients. In our previous work, we found that immunotherapy alone did not improve survival in our mouse models. However, when we combined it with two additional therapies that activate immune cells, survival dramatically increased and 50% of the treated mice became completely tumor-free. In this project, we will study what changes occur in the immune system with this treatment that led to this strong anti-tumor response. We hypothesize that a group of immune cells called innate lymphoid cells play a key role by activating other immune cells, such as T cells and B cells, to enhance their ability to destroy cancer cells. To test this, we will treat mice with and without our triple-therapy combination, collect their tumors, and analyze the immune cells to understand how the treatment reshapes the immune environment. By uncovering how this therapy activates the immune system, we hope to identify new ways to make it even more effective. Ultimately, our findings could pave the way for moving this treatment into clinical trials, bringing us closer to improving survival and outcomes for people with ovarian cancer.
Department
Program
DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
Recipient
Location
Ontario, Canada
Recipient Type
Other
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
559292
Name
Ibrahim Dalia K
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
DT1 (Biomedical and/or Clinical Research) CGRS Doctoral
Projecttitle
Harnessing IL-33 and Checkpoint Blockade to Boost Adaptive Immunity in Ovarian Cancer
Programtype2
Studentship Programs
Orgnameinp2
Ottawa Hospital Research Institute
Cihramount2
$120,000
Cihrequipment2
$0
Programname2
DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
Keyworddelim
Checkpoint Blockade; Immune System; Immunotherapy; Mouse Models; Ovarian Cancer; Spatial Transcriptomics; Tumor Microenvironment
Abstract
Survival rates for ovarian cancer have remained largely unchanged for decades, partly because current treatments are not effective enough to cure patients. One promising strategy is immunotherapy, which strengthens the body's own immune system to fight cancer. While this approach has been very successful in other cancer types, it has not worked well for ovarian cancer. Our research aims to develop more effective immunotherapies for ovarian cancer using clinically relevant mouse models that closely mimic human disease. We believe that by gaining a deeper understanding of how the immune system interacts with ovarian tumors, we can design better treatments for patients. In our previous work, we found that immunotherapy alone did not improve survival in our mouse models. However, when we combined it with two additional therapies that activate immune cells, survival dramatically increased and 50% of the treated mice became completely tumor-free. In this project, we will study what changes occur in the immune system with this treatment that led to this strong anti-tumor response. We hypothesize that a group of immune cells called innate lymphoid cells play a key role by activating other immune cells, such as T cells and B cells, to enhance their ability to destroy cancer cells. To test this, we will treat mice with and without our triple-therapy combination, collect their tumors, and analyze the immune cells to understand how the treatment reshapes the immune environment. By uncovering how this therapy activates the immune system, we hope to identify new ways to make it even more effective. Ultimately, our findings could pave the way for moving this treatment into clinical trials, bringing us closer to improving survival and outcomes for people with ovarian cancer.
Competitiondate
202511
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Ibrahim, Dalia K
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $120,000~ $0~