Downregulation of MICA/MICB improves cell persistence and clinical activity of NKG2DL CAR T-cells in patients with relapsed or refractory acute myeloid leukemia or myelodysplastic neoplasia. - 2025
Downregulation of MICA/MICB improves cell persistence and clinical activity of NKG2DL CAR T-cells in patients with relapsed or refractory acute myeloid leukemia or myelodysplastic neoplasia.
[en] The NKG2D receptor binds eight ligands (NKG2DL) overexpressed in a wide range of malignancies, but largely absent on non-neoplastic cells. Initial clinical evaluation of NKG2DL chimeric antigen receptor (CAR) T-cells (CYAD-01) in patients with relapsed or refractory (r/r) acute myeloid leukemia (AML) or myelodysplastic neoplasia (MDS) demonstrated low durability of responses and short cell persistence. Two Phase I trials were initiated to evaluate the effect of lymphodepletion prior to a single CAR T-cell infusion in a similar r/r AML/MDS patient population. The DEPLETHINK trial (NCT03466320) evaluated CYAD-01 while the CYCLE-1 trial (NCT04167696) evaluated a next-generation NKG2DL CAR, CYAD-02, where the two main NKG2D ligands MICA and B are downregulated, to increase CAR T-cell persistence. Seventeen and twelve patients were treated in the DEPLETHINK and CYCLE-1 trials, and confirmed the good tolerability of both products with cytokine release syndrome (CRS) grade 3 or 4 reported in 25% and 33.3% of patients, respectively. CYAD-02 presented an higher engraftment and an improved clinical activity (17% objective response rate) compared to CYAD-01 (no objective response). Altogether, our data provide proof of principle that knock-down of MICA/B can enhance CAR T-cell persistence and efficacy while maintaining a good safety profile.
Disciplines :
Hematology
Author, co-author :
Pollyea, Daniel; University of Colorado Denver (UCD), Denver, USA
Downregulation of MICA/MICB improves cell persistence and clinical activity of NKG2DL CAR T-cells in patients with relapsed or refractory acute myeloid leukemia or myelodysplastic neoplasia.
We thank all former colleagues at Celyad Oncology who might have contributed to this work. The two clinical trials (CYCLE-1 and DEPLETHINK) were sponsored by Celyad Oncology SA, which provided all the trial materials. We thank the patients who participated in the trials, their families, friends, and caregivers, but also the trial staffs and healthcare providers at all the clinical trial sites for their commitment and support during the trial conduct.
Labanieh L Mackall CL CAR immune cells: design principles, resistance and the next generation Nature 2023 614 635 48 1:CAS:528:DC%2BB3sXjslGhtrc%3D 10.1038/s41586-023-05707-3 36813894
Mitra A Barua A Huang L Ganguly S Feng Q He B From bench to bedside: the history and progress of CAR T cell therapy Front Immunol 2023 14 1:CAS:528:DC%2BB3sXht1ehtrzF 10.3389/fimmu.2023.1188049 37256141 10225594 1188049
Dagar G Gupta A Masoodi T Nisar S Merhi M Hashem S et al. Harnessing the potential of CAR-T cell therapy: progress, challenges, and future directions in hematological and solid tumor treatments J Transl Med 2023 21 10.1186/s12967-023-04292-3 37420216 10327392 449
Iyer P Jasdanwala SS Wang Y Bhatia K Bhatt S Decoding acute myeloid leukemia: a clinician’s guide to functional profiling Diagnostics (Basel) 2024 14 2560 1:CAS:528:DC%2BB2MXktFKrurY%3D 10.3390/diagnostics14222560 39594226
Epperly R Gottschalk S Velasquez MP A bump in the road: how the hostile AML microenvironment affects CAR T cell therapy Front Oncol 2020 10 262 10.3389/fonc.2020.00262 32185132 7058784
Tettamanti S Pievani A Biondi A Dotti G Serafini M Catch me if you can: how AML and its niche escape immunotherapy Leukemia 2022 36 13 22 10.1038/s41375-021-01350-x 34302116
NCCN. NCCN guidelines for acute myeloid leukemia version 2.2025. NCCN 2025. https://www.nccn.org/guidelines/guidelines-detail?category=1&id=1411. Accessed 22 Apr 2025).
Damiani D Tiribelli M CAR-T cells in acute myeloid leukemia: where do we stand? Biomedicines 2024 12 1194 1:CAS:528:DC%2BB2cXitlWlsr%2FJ 10.3390/biomedicines12061194 38927401 11200794
Bhagwat AS Torres L Shestova O Shestov M Mellors PW Fisher HR et al. Cytokine-mediated CAR T therapy resistance in AML Nat Med 2024 30 3697 708 1:CAS:528:DC%2BB2cXitFWht7fO 10.1038/s41591-024-03271-5 39333315 12118809
Raulet DH Roles of the NKG2D immunoreceptor and its ligands Nat Rev Immunol 2003 3 781 90 1:CAS:528:DC%2BD3sXoslSgsb0%3D 10.1038/nri1199 14523385
Spear P Wu M-R Sentman M-L Sentman CL NKG2D ligands as therapeutic targets Cancer Immun 2013 13 8 23833565 3700746
Demoulin B Cook WJ Murad J Graber DJ Sentman M-L Lonez C et al. Exploiting natural killer group 2D receptors for CAR T-cell therapy Future Oncol 2017 13 1593 605 1:CAS:528:DC%2BC2sXhtl2gs7zO 10.2217/fon-2017-0102 28613086
Sallman DA Brayer J Sagatys EM Lonez C Breman E Agaugué S et al. NKG2D-based chimeric antigen receptor therapy induced remission in a relapsed/refractory acute myeloid leukemia patient Haematologica 2018 103 e424 6 10.3324/haematol.2017.186742 29703727 6119132
Sallman DA Kerre T Havelange V Poiré X Lewalle P Wang ES et al. CYAD-01, an autologous NKG2D-based CAR T-cell therapy, in relapsed or refractory acute myeloid leukaemia and myelodysplastic syndromes or multiple myeloma (THINK): haematological cohorts of the dose escalation segment of a phase 1 trial Lancet Haematol 2023 10 e191 202 1:CAS:528:DC%2BB3sXivVKku7c%3D 10.1016/S2352-3026(22)00378-7 36764323
Hendlisz A Rottey S Opyrchal M Odunsi K Machiels J-P Sahebjam S et al. Results and perspectives from Phase 1 studies assessing the safety and clinical activity of multiple doses of a NKG2D-based CAR-T therapy, CYAD-01, in metastatic solid tumors J Immunother Cancer 2018 6 114
Lonez C Verma B Hendlisz A Aftimos P Awada A Van Den Neste E et al. Study protocol for THINK: a multinational open-label phase I study to assess the safety and clinical activity of multiple administrations of NKR-2 in patients with different metastatic tumour types BMJ Open 2017 7 e017075 10.1136/bmjopen-2017-017075 29133316 5695348
Breman E Demoulin B Agaugué S Mauën S Michaux A Springuel L et al. Overcoming target driven fratricide for T cell therapy Front Immunol 2018 9 2940 1:CAS:528:DC%2BC1MXht1eqtLzN 10.3389/fimmu.2018.02940 30619300 6299907
Caracciolo D Mancuso A Polerà N Froio C D’Aquino G Riillo C et al. The emerging scenario of immunotherapy for T-cell Acute Lymphoblastic Leukemia: advances, challenges and future perspectives Exp Hematol Oncol 2023 12 5 1:CAS:528:DC%2BB3sXoslCgtQ%3D%3D 10.1186/s40164-022-00368-w 36624522 9828428
Rossi M Steklov M Huberty F Nguyen T Marijsse J Jacques-Hespel C et al. Efficient shRNA-based knockdown of multiple target genes for cell therapy using a chimeric miRNA cluster platform Mol Ther Nucleic Acids 2023 34 1:CAS:528:DC%2BB3sXitVehs7bP 10.1016/j.omtn.2023.102038 37799328 10548280 102038
Lonez C Bolsée J Huberty F Nguyen T Jacques-Hespel C Anguille S et al. Clinical proof-of-concept of a non-gene editing technology using miRNA-based shRNA to engineer allogeneic CAR T-cells Int J Mol Sci 2025 26 1658 1:CAS:528:DC%2BB2MXltl2qsLo%3D 10.3390/ijms26041658 40004122 11855736
Döhner H Estey E Grimwade D Amadori S Appelbaum FR Büchner T et al. Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel Blood 2017 129 424 47 10.1182/blood-2016-08-733196 27895058 5291965
Greenberg PL Tuechler H Schanz J Sanz G Garcia-Manero G Solé F et al. Revised International Prognostic Scoring System for myelodysplastic syndromes Blood 2012 120 2454 65 1:CAS:528:DC%2BC38XhsVKiu73K 10.1182/blood-2012-03-420489 22740453 4425443
Cheson BD Bennett JM Kopecky KJ Büchner T Willman CL Estey EH et al. Revised recommendations of the International Working Group for Diagnosis, Standardization of Response Criteria, Treatment Outcomes, and Reporting Standards for therapeutic trials in acute myeloid leukemia J Clin Oncol 2003 21 4642 9 10.1200/JCO.2003.04.036 14673054
Cheson BD Greenberg PL Bennett JM Lowenberg B Wijermans PW Nimer SD et al. Clinical application and proposal for modification of the International Working Group (IWG) response criteria in myelodysplasia Blood 2006 108 419 25 1:CAS:528:DC%2BD28XntFehtrk%3D 10.1182/blood-2005-10-4149 16609072
Neelapu SS Tummala S Kebriaei P Wierda W Gutierrez C Locke FL et al. Chimeric antigen receptor T-cell therapy — assessment and management of toxicities Nat Rev Clin Oncol 2018 15 47 62 1:CAS:528:DC%2BC2sXhsFWnur%2FN 10.1038/nrclinonc.2017.148 28925994
Lee DW Santomasso BD Locke FL Ghobadi A Turtle CJ Brudno JN et al. ASTCT consensus grading for cytokine release syndrome and neurologic toxicity associated with immune effector cells Biol Blood Marrow Transpl 2019 25 625 38 1:CAS:528:DC%2BC1MXhs1aksbw%3D 10.1016/j.bbmt.2018.12.758
Haubner S Subklewe M Sadelain M Honing CAR T cells to tackle acute myeloid leukemia Blood 2025 145 1113 25 1:CAS:528:DC%2BB2MXovVansrk%3D 10.1182/blood.2024024063 39630061
Saito S Nakazawa Y CAR-T cell therapy in AML: recent progress and future perspectives Int J Hematol 2024 120 455 66 10.1007/s12185-024-03809-w 38963636
Shah NN Tasian SK Kohler ME Hsieh EM Baumeister SHC Summers C et al. CD33 CAR T-cells (CD33CART) for children and young adults with relapsed/refractory AML: dose-escalation results from a phase I/II multicenter trial Blood 2023 142 771 10.1182/blood-2023-179667
Zhao Y Zhang X Zhang M Guo R Zhang Y Pu Y et al. Modified EASIX scores predict severe CRS/ICANS in patients with acute myeloid leukemia following CLL1 CAR-T cell therapy Ann Hematol 2024 103 969 80 1:CAS:528:DC%2BB2cXht1Whu7k%3D 10.1007/s00277-024-05617-y 38214708
Xu J Zhang H Zhao Y Zhang X Guo S Shi X et al. Infectious complications distribution following CLL1 CAR-T cell therapy for acute myeloid leukemiass Cancer Immunol Immunother 2025 74 149 1:CAS:528:DC%2BB2MXms1Sht7s%3D 10.1007/s00262-025-03998-1 40088283 11910464
Barber A Rynda A Sentman CL Chimeric NKG2D expressing T cells eliminate immunosuppression and activate immunity within the ovarian tumor microenvironment J Immunol 2009 183 6939 47 1:CAS:528:DC%2BD1MXhsVehsLbO 10.4049/jimmunol.0902000 19915047
Zhang T Sentman CL Mouse tumor vasculature expresses NKG2D ligands and can be targeted by chimeric NKG2D-modified T cells J Immunol 2013 190 2455 63 1:CAS:528:DC%2BC3sXislOls7g%3D 10.4049/jimmunol.1201314 23355740
Tan G Spillane KM Maher J The role and regulation of the NKG2D/NKG2D ligand system in cancer Biology 2023 12 1079 10.3390/biology12081079 37626965 10452210
Agaugue S Hargreaves A De Sousa P De Waele P Gilham D The high expression of NKG2D ligands on tumor and the lack of surface expression on healthy tissues provides a strong rationale to support NKG2D-based therapeutic approaches for cancer Ann Oncol 2018 29 viii420 10.1093/annonc/mdy288.052
Subklewe M Bücklein V Sallman D Daver N Novel immunotherapies in the treatment of AML: is there hope? Hematol Am Soc Hematol Educ Program 2023 2023 691 701 10.1182/hematology.2023000455
Yang X Ma L Zhang X Huang L Wei J Targeting PD-1/PD-L1 pathway in myelodysplastic syndromes and acute myeloid leukemia Exp Hematol Oncol 2022 11 11 1:CAS:528:DC%2BB38XhtVWnsb7J 10.1186/s40164-022-00263-4 35236415 8889667
Haroun F Solola SA Nassereddine S Tabbara I PD-1 signaling and inhibition in AML and MDS Ann Hematol 2017 96 1441 8 1:CAS:528:DC%2BC2sXhtVOjsL3L 10.1007/s00277-017-3051-5 28643044
Luciano M Krenn PW Horejs-Hoeck J The cytokine network in acute myeloid leukemia Front Immunol 2022 13 1:CAS:528:DC%2BB38XisleiurfI 10.3389/fimmu.2022.1000996 36248849 9554002 1000996
Bolsée J, Violle B, Jacques-Hespel C, Nguyen T, Lonez C, Breman E. Tandem CAR T-cells targeting CD19 and NKG2DL can overcome CD19 antigen escape in B-ALL. Front Immunol. 2025;16:1557405.
Wang H, Feng S, Zhu Y, Zhang Y, Zhou Z, Nian Z, et al. The tandem CD33-CLL1 CAR-T as an approach to treat acute myeloid leukemia. Blood Transfus. 2025;23:338–47.
Strickland SA Eghtedar A Farhadfar N Bajel AR Ravandi F Emery R et al. Abstract CT014: first-in-human, multicenter study of SENTI-202, a CD33/FLT3 selective off-the-shelf logic gated CAR NK cell therapy in hematologic malignancies including AML: clinical data Cancer Res 2025 85 CT014 10.1158/1538-7445.AM2025-CT014