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Grant: Project Grant

University of Toronto

$1,071,000.00

B cell Immunotherapy for the treatment of Acute Myeloid Leukemia

FY 2025-26

Summary
Acute myeloid leukemia (AML) is the deadliest hematological malignancy, especially amongst older adults. Chemotherapy is the frontline treatment option for AML, achieving high remission rates (~70%) amongst patients. Yet, nearly half will experience disease relapse, with a significant risk of recurrence lasting for at least five years post-remission. Emergent findings suggest that chemotherapy-resistant AML cells persists within treated patients, requiring more targeted strategies for complete disease elimination. Consequently, immunotherapies have gained significant traction due to the sustained and targeted responses that they can achieve towards AML. However, traditional immunotherapies primarily focus on T cells, achieving limited success against AML due to hindered function of T cells within AML patients. Therefore, we propose to develop a B cell based therapy that can generate AML targeting antibodies directly within patients. In this manner, we will provide an innovative strategy that can overcome the limitations of current therapies to effectively eliminate AML.
Program
Project Grant
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
533983
Name
Aung Aereas
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Biology & Therapeutics
Projecttitle
B cell Immunotherapy for the treatment of Acute Myeloid Leukemia
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$1,071,000
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Acute Myeloid Leukemia; Immunotherapy; Vaccines
Abstract
Acute myeloid leukemia (AML) is the deadliest hematological malignancy, especially amongst older adults. Chemotherapy is the frontline treatment option for AML, achieving high remission rates (~70%) amongst patients. Yet, nearly half will experience disease relapse, with a significant risk of recurrence lasting for at least five years post-remission. Emergent findings suggest that chemotherapy-resistant AML cells persists within treated patients, requiring more targeted strategies for complete disease elimination. Consequently, immunotherapies have gained significant traction due to the sustained and targeted responses that they can achieve towards AML. However, traditional immunotherapies primarily focus on T cells, achieving limited success against AML due to hindered function of T cells within AML patients. Therefore, we propose to develop a B cell based therapy that can generate AML targeting antibodies directly within patients. In this manner, we will provide an innovative strategy that can overcome the limitations of current therapies to effectively eliminate AML.
Competitiondate
202509
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Aung, Aereas
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,071,000~ $0~