Thoas Fioretos
Research team manager
Antibodies targeting human IL1RAP (IL1R3) show therapeutic effects in xenograft models of acute myeloid leukemia.
Author
Summary, in English
Acute myeloid leukemia (AML) is associated with a poor survival rate, and there is an urgent need for novel and more efficient therapies, ideally targeting AML stem cells that are essential for maintaining the disease. The interleukin 1 receptor accessory protein (IL1RAP; IL1R3) is expressed on candidate leukemic stem cells in the majority of AML patients, but not on normal hematopoietic stem cells. We show here that monoclonal antibodies targeting IL1RAP have strong antileukemic effects in xenograft models of human AML. We demonstrate that effector-cell-mediated killing is essential for the observed therapeutic effects and that natural killer cells constitute a critical human effector cell type. Because IL-1 signaling is important for the growth of AML cells, we generated an IL1RAP-targeting antibody capable of blocking IL-1 signaling and show that this antibody suppresses the proliferation of primary human AML cells. Hence, IL1RAP can be efficiently targeted with an anti-IL1RAP antibody capable of both achieving antibody-dependent cellular cytotoxicity and blocking of IL-1 signaling as modes of action. Collectively, these results provide important evidence in support of IL1RAP as a target for antibody-based treatment of AML.
Department/s
- Translational Genomic and Functional Studies of Leukemia
- Division of Clinical Genetics
- Division of Molecular Medicine and Gene Therapy
- BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation
- Stem Cell Center
- Targeted therapies in leukemia
- StemTherapy: National Initiative on Stem Cells for Regenerative Therapy
Publishing year
2015
Language
English
Pages
10786-10791
Publication/Series
Proceedings of the National Academy of Sciences
Volume
112
Issue
34
Full text
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Links
Document type
Journal article
Publisher
National Academy of Sciences
Topic
- Hematology
Status
Published
Research group
- Translational Genomic and Functional Studies of Leukemia
- Targeted therapies in leukemia
ISBN/ISSN/Other
- ISSN: 1091-6490