Article
CAR T cell therapy selectively depletes disease-driving mutant calreticulin cells in xenotransplants and human organoid models of myelofibrosis.
Science translational medicine - 1 Jul 2026
Rampotas Alexandros, Wong Zoë C, Gannon Isaac, Brierley Charlotte K, Shen Yuqi, Benlabiod Camelia, Chee Ashlyn, Khan Saif, Hayder Nawshad, Cheung Gordon Weng-Kit, Mitsikakou Marina, Murphy Eleanor, Ferrari Mathieu, Bulek Anna, Rodriguez-Romera Antonio, Murphy Lauren, Olijnik Aude-Anais, Rodriguez-Justo Manuel, Marty Caroline, Hitchcock Ian, Royston Daniel, Mead Adam J, Khan Abdullah O, Lambert Jonathan, Roddie Claire, Psaila Bethan, Pule Martin A
Abstract excerpt
Targeted immunotherapies have revolutionized outcomes for lymphoid malignancies, but success in myeloid neoplasms is limited by the lack of amenable targets and immunologically hostile tumor microenvironment (TME). Myeloproliferative neoplasms (MPNs) are chronic myeloid blood cancers, a third of which are driven by mutations in calreticulin. Calreticulin mutant protein (mutCALR) binds and activates thrombopoietin...
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