Blood cancer discoveryJournal Article
05 May 2025
Our investigation of the SOCS1 pathway in AML and T-cell interactions provides insights into potential mechanisms of resistance of AML to allogeneic hematopoietic stem cell transplantation and demonstrates the potential of targeting SOCS1 and its downstream mediators to enhance antileukemic T-cell activity.
See related commentary by Fry, p. 157.
S. Rutella reports grants from Wugen outside the submitted work. A.D. Schimmer reports personal fees from Takeda Pharmaceuticals, Bristol Myers Squibb, AstraZeneca, and Novartis and grants from Takeda Pharmaceuticals and Medivir outside the submitted work; a patent for DNT Cells for the Treatment of Leukemia pending; and being on the medical and scientific board of The Leukemia and Lymphoma Society of Canada. A.D. Schimmer is an inventor of DNT cell technology–related patents and intellectual properties for the treatment of AML. J. Lee reports a patent for US10517937 issued, a patent for US11020157 issued, a patent for US17/415957 pending, and a patent for US17/797630 pending. L. Zhang reports grants from Canadian Institutes of Health Research (grant #419699) and Canadian Cancer Society Impact Grant (grant #704121) during the conduct of the study; other support from Wyze Biotech Co. Ltd. outside the submitted work; a patent 4 issued, a patent 4 pending, and a patent 1 licensed; and having financial interests (e.g., holdings/shares) in Wyze Biotech Co. Ltd. and previously received research funding and consulting fee/honorarium from the company. No disclosures were reported by the other authors.
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