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Self-driving armored CAR-T cells overcome a suppressive milieu and eradicate CD19 + Raji lymphoma in preclinical models.
- Source :
-
Molecular therapy : the journal of the American Society of Gene Therapy [Mol Ther] 2021 Sep 01; Vol. 29 (9), pp. 2691-2706. Date of Electronic Publication: 2021 May 08. - Publication Year :
- 2021
-
Abstract
- Chimeric antigen receptor (CAR) T cells typically use a strong constitutive promoter to ensure maximal long-term CAR expression. However, recent evidence suggests that restricting the timing and magnitude of CAR expression is functionally beneficial, whereas constitutive CAR activation may lead to exhaustion and loss of function. We created a self-driving CD19-targeting CAR, which regulates its own function based on the presence of a CD19 antigen engaged by the CAR itself, by placing self-driving CAR19 constructs under transcriptional control of synthetic activator protein 1 (AP1)-nuclear factor κB (NF-κB) or signal transducer and activator of transcription (STAT)5 promoters. CD19 antigen-regulated expression was observed for self-driving AP1-NFκB-CAR19, with CAR19 upregulation within 18 h after exposure to target CD19, and corresponded to the level of tumor burden. Self-driving CAR-T cells showed enhanced tumor-dependent activation, expansion, and low exhaustion in vitro as compared to constitutively expressed EF1α and murine stem cell virus (MSCV) CARs and mediated tumor regression and survival in Raji-bearing NOD.Cg-Prkdc <superscript>scid</superscript> Il2rg <superscript>tm1Wjl</superscript> /SzJ (NSG) mice. Long-term CAR function correlated with upregulated CAR expression within 24 h of exposure to tumor antigen. The self-driving AP1-NFκB-CAR19 circuit was also used to inducibly express dominant-negative transforming growth factor β receptor II (TGFBRIIdn), which effectively countered the negative effects of TGF-β on CAR-T activation. Thus, a self-driving CAR approach may offer a new modality to express CAR and auxiliary proteins by enhancing CAR-T functional activity and limiting exhaustion.<br />Competing Interests: Declaration of interests D.S., B.D., and B.W. have submitted a patent application regarding treating cancer with self-driving chimeric antigen receptors (PCT/US2020/021320) on the basis of this work. This study was funded by Lentigen Technology, a Miltenyi Biotec Company, and Miltenyi Biotec. Y.X., P.H., D.W., L.A., D.S., and B.D. are employees of Lentigen, a Miltenyi Biotec company, and B.W. is an employee of Miltenyi Biotec.<br /> (Copyright © 2021 The American Society of Gene and Cell Therapy. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Burkitt Lymphoma genetics
Burkitt Lymphoma immunology
Burkitt Lymphoma pathology
Cell Line, Tumor
HEK293 Cells
Humans
K562 Cells
Mice
Mice, Inbred NOD
Promoter Regions, Genetic
Xenograft Model Antitumor Assays
Burkitt Lymphoma therapy
Immunotherapy, Adoptive methods
NF-kappa B genetics
Receptor, Transforming Growth Factor-beta Type II genetics
Receptors, Antigen, T-Cell metabolism
STAT5 Transcription Factor genetics
Transcription Factor AP-1 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1525-0024
- Volume :
- 29
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Molecular therapy : the journal of the American Society of Gene Therapy
- Publication Type :
- Academic Journal
- Accession number :
- 33974997
- Full Text :
- https://doi.org/10.1016/j.ymthe.2021.05.006