Antibodies targeting human IL1RAP (IL1R3) show therapeutic effects in xenograft models of acute myeloid leukemia.
(2015) In Proceedings of the National Academy of Sciences 112(34). p.10786-10791- Abstract
- 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... (More)
- 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. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/7844248
- author
- organization
-
- Translational Genomic and Functional Studies of Leukemia (research group)
- 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 (research group)
- StemTherapy: National Initiative on Stem Cells for Regenerative Therapy
- publishing date
- 2015
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Proceedings of the National Academy of Sciences
- volume
- 112
- issue
- 34
- pages
- 10786 - 10791
- publisher
- National Academy of Sciences
- external identifiers
-
- wos:000360005600068
- pmid:26261316
- scopus:84940544514
- pmid:26261316
- ISSN
- 1091-6490
- DOI
- 10.1073/pnas.1422749112
- language
- English
- LU publication?
- yes
- id
- 0c5154c0-8f8a-4061-9e5d-2f05e0072441 (old id 7844248)
- alternative location
- http://www.ncbi.nlm.nih.gov/pubmed/26261316?dopt=Abstract
- date added to LUP
- 2016-04-01 11:15:18
- date last changed
- 2022-08-13 02:42:00
@article{0c5154c0-8f8a-4061-9e5d-2f05e0072441, abstract = {{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.}}, author = {{Ågerstam, Helena and Karlsson, Christine and Hansen, Nils and Sandén, Carl and Askmyr, Maria and von Palffy, Sofia and Högberg, Carl and Rissler, Marianne and Wunderlich, Mark and Juliusson, Gunnar and Richter, Johan and Sjöström, Kjell and Bhatia, Ravi and Mulloy, James C and Järås, Marcus and Fioretos, Thoas}}, issn = {{1091-6490}}, language = {{eng}}, number = {{34}}, pages = {{10786--10791}}, publisher = {{National Academy of Sciences}}, series = {{Proceedings of the National Academy of Sciences}}, title = {{Antibodies targeting human IL1RAP (IL1R3) show therapeutic effects in xenograft models of acute myeloid leukemia.}}, url = {{https://lup.lub.lu.se/search/files/2509956/8000943}}, doi = {{10.1073/pnas.1422749112}}, volume = {{112}}, year = {{2015}}, }