CD37 is a safe chimeric antigen receptor target to treat acute myeloid leukemia

被引:5
作者
Caulier, Benjamin [1 ,2 ,3 ]
Joaquina, Sandy [1 ]
Gelebart, Pascal [4 ,6 ]
Dowling, Tara Helen [4 ,5 ,6 ]
Kaveh, Fatemeh [1 ]
Thomas, Moritz [7 ,8 ]
Tandaric, Luka [6 ,9 ]
Wernhoff, Patrik [1 ]
Katyayini, Niveditha Umesh [2 ,3 ]
Wogsland, Cara [4 ,6 ]
Gjerstad, May Eriksen [4 ,6 ]
Floisand, Yngvar [2 ]
Kvalheim, Gunnar [1 ]
Marr, Carsten [7 ]
Kobold, Sebastian [10 ,11 ,12 ]
Enserink, Jorrit M. [2 ,3 ,13 ]
Gjertsen, Bjorn Tore [6 ,14 ]
McCormack, Emmet [4 ,5 ,6 ]
Inderberg, Else Marit [1 ]
Walchli, Sebastien [1 ]
机构
[1] Oslo Univ Hosp, Dept Oncol, Translat Res Unit, Sect Cellular Therapy, Oslo, Norway
[2] Oslo Univ Hosp, Inst Canc Res, Dept Mol Cell Biol, Oslo, Norway
[3] Univ Oslo, Inst Clin Med, Fac Med, Ctr Canc Cell Reprogramming CanCell, Oslo, Norway
[4] Univ Bergen, Dept Clin Sci, Precis Oncol Res Grp, N-5021 Bergen, Norway
[5] Univ Bergen, Ctr Pharm, Dept Clin Sci, Bergen, Norway
[6] Univ Bergen, Ctr Canc Biomarkers CCBIO, Bergen, Norway
[7] Helmholtz Munich, Inst AI Hlth, D-85764 Neuherberg, Germany
[8] Tech Univ Munich, Sch Life Sci Weihenstephan, Freising Weihenstephan, Germany
[9] Haukeland Hosp, Dept Obstet & Gynecol, Bergen, Norway
[10] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Med 4, Div Clin Pharmacol, Munich, Germany
[11] German Ctr Translat Canc Res DKTK, Partner Site Munich, Munich, Germany
[12] Helmholtz Zent Munchen, Res Ctr Environm Hlth HMGU, Einheit Klin Pharmakol EKLiP, Neuherberg, Germany
[13] Univ Oslo, Fac Math & Nat Sci, Sect Biochem & Mol Biol, Oslo, Norway
[14] Haukeland Hosp, Dept Med, Dept Med, Bergen, Norway
基金
欧洲研究理事会; 欧盟地平线“2020”;
关键词
CAR T-CELL; ANTIBODY-DRUG CONJUGATE; EXPRESSION; AML; EFFICACY; SIGLEC-6; THERAPY; PROTEIN; CANCER;
D O I
10.1016/j.xcrm.2024.101572
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Acute myeloid leukemia (AML) is characterized by the accumulation of immature myeloid cells in the bone marrow and the peripheral blood. Nearly half of the AML patients relapse after standard induction therapy, and new forms of therapy are urgently needed. Chimeric antigen receptor (CAR) T therapy has so far not been successful in AML due to lack of efficacy and safety. Indeed, the most attractive antigen targets are stem cell markers such as CD33 or CD123. We demonstrate that CD37, a mature B cell marker, is expressed in AML samples, and its presence correlates with the European LeukemiaNet (ELN) 2017 risk stratification. We repurpose the anti -lymphoma CD37CAR for the treatment of AML and show that CD37CAR T cells specifically kill AML cells, secrete proinflammatory cytokines, and control cancer progression in vivo . Importantly, CD37CAR T cells display no toxicity toward hematopoietic stem cells. Thus, CD37 is a promising and safe CAR T cell AML target.
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页数:28
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