| Literature DB >> 27621309 |
Helena Ågerstam1, Nils Hansen1, Sofia von Palffy1, Carl Sandén1, Kristian Reckzeh1, Christine Karlsson1, Henrik Lilljebjörn1, Niklas Landberg1, Maria Askmyr1, Carl Högberg1, Marianne Rissler1, Kimmo Porkka2, Hans Wadenvik3, Satu Mustjoki2, Johan Richter4, Marcus Järås1, Thoas Fioretos1.
Abstract
Chronic myeloid leukemia (CML) is currently treated with tyrosine kinase inhibitors, but these do not effectively eliminate the CML stem cells. As a consequence, CML stem cells persist and cause relapse in most patients upon drug discontinuation. Furthermore, no effective therapy exists for the advanced stages of the disease. Interleukin-1 receptor accessory protein (IL1RAP; IL1R3) is a coreceptor of interleukin-1 receptor type 1 and has been found upregulated on CML stem cells. Here, we show that primitive (CD34+CD38-) CML cells, in contrast to corresponding normal cells, express a functional interleukin-1 (IL-1) receptor complex and respond with NF-κB activation and marked proliferation in response to IL-1. IL1RAP antibodies that inhibit IL-1 signaling could block these effects. In vivo administration of IL1RAP antibodies in mice transplanted with chronic and blast phase CML cells resulted in therapeutic effects mediated by murine effector cells. These results provide novel insights into the role of IL1RAP in CML and a strong rationale for the development of an IL1RAP antibody therapy to target residual CML stem cells.Entities:
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Year: 2016 PMID: 27621309 DOI: 10.1182/blood-2015-11-679985
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113