High-Specificity CRISPR-Mediated Genome Engineering in Anti-BCMA Allogeneic CAR T Cells Suppresses Allograft Rejection in Preclinical Models.
Émilie DegagnéPaul D DonohoueSuparna RoyJessica SchererTristan W FowlerRyan T DavisGustavo A ReyesGeorge KwongMorena StanawayVanina Larroca VicenaDevin MuthaRaymond GuoLeslie EdwardsBenjamin SchillingMcKay ShawStephen C SmithBryan KohrsHeinrich J KufeldtGlen ChurchwardFiney RuanDavid B NyerKyle McSweeneyMatthew J IrbyChristopher K FullerLynda BanhMckenzi S TohMatthew ThompsonArthur L G OwenZili AnScott GradiaJustin SkobleMara BryanElizabeth GarnerSteven B KannerPublished in: Cancer immunology research (2024)
Allogeneic chimeric antigen receptor (CAR) T cell therapies hold the potential to overcome many of the challenges associated with patient-derived (autologous) CAR T cells. Key considerations in the development of allogeneic CAR T cell therapies include prevention of graft-vs-host disease (GvHD) and suppression of allograft rejection. Here, we describe preclinical data supporting the ongoing first-in-human clinical study, the CaMMouflage trial (NCT05722418), evaluating CB-011 in patients with relapsed/refractory multiple myeloma. CB-011 is a hypoimmunogenic, allogeneic anti-B-cell maturation antigen (BCMA) CAR T cell therapy candidate. CB-011 cells feature 4 genomic alterations and were engineered from healthy donor-derived T cells using a Cas12a CRISPR hybrid RNA-DNA (chRDNA) genome-editing technology platform. To address allograft rejection, CAR T cells were engineered to prevent endogenous HLA class I complex expression and overexpress a single-chain polyprotein complex composed of beta-2 microglobulin (B2M) tethered to HLA-E. In addition, T-cell receptor (TCR) expression was disrupted at the TCR alpha constant locus in combination with the site-specific insertion of a humanized BCMA-specific CAR. CB-011 cells exhibited robust plasmablast cytotoxicity in vitro in a mixed lymphocyte reaction in cell cocultures derived from patients with multiple myeloma. In addition, CB-011 cells demonstrated suppressed recognition by and cytotoxicity from HLA-mismatched T cells. CB-011 cells were protected from natural killer cell-mediated cytotoxicity in vitro and in vivo due to endogenous promoter-driven expression of B2M-HLA-E. Potent antitumor efficacy, when combined with an immune-cloaking armoring strategy to dampen allograft rejection, offers optimized therapeutic potential in multiple myeloma. See related Spotlight by Caimi and Melenhorst, p. 385.
Keyphrases
- cell therapy
- genome editing
- multiple myeloma
- induced apoptosis
- crispr cas
- stem cell transplantation
- cell cycle arrest
- bone marrow
- poor prognosis
- stem cells
- gene expression
- endoplasmic reticulum stress
- endothelial cells
- signaling pathway
- binding protein
- cell death
- clinical trial
- oxidative stress
- mesenchymal stem cells
- randomized controlled trial
- regulatory t cells
- acute lymphoblastic leukemia
- pi k akt
- cell proliferation
- transcription factor
- risk assessment
- big data
- high dose
- high throughput
- cell free