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DRUG:

CD229 CAR T

i
Other names: CD229 CAR T
Associations
Trials
Company:
University of Utah
Drug class:
CD229-targeted CAR-T immunotherapy
Associations
Trials
over2years
Systematic single amino acid affinity tuning of CD229 CAR T cells retains efficacy against multiple myeloma and eliminates on-target off-tumor toxicity. (PubMed, Sci Transl Med)
We identified a CD229 CAR binding domain with micromolar affinity that, when combined with overexpression of c-Jun, confers antitumor activity comparable to parental CD229 CAR T cells but lacks the parental cells' cytotoxic activity toward healthy lymphocytes in vitro and in vivo. The results represent a promising strategy to improve the efficacy and safety of CAR T cell therapy that requires clinical validation.
Journal • CAR T-Cell Therapy
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LY9 (Lymphocyte Antigen 9) • JUN (Jun proto-oncogene)
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LY9 expression
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CD229 CAR T
over4years
CD229 CAR T Cell Therapy for the Treatment of Relapsed B Cell Lymphoma (ASH 2021)
Finally, CD229 CAR T cells are effective against primary CLL cells from patients that have relapsed from CD19 CAR T cell therapy and do no exhibit antigen loss by trogocytosis. Taken together, these data suggest that CD229 CAR T cell therapy may be a promising option to address the poor outcomes for patients with relapsed B cell lymphoma.
CAR T-Cell Therapy
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CD19 (CD19 Molecule) • IFNG (Interferon, gamma) • IL2 (Interleukin 2) • LY9 (Lymphocyte Antigen 9)
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CD19 expression • LY9 expression
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CD229 CAR T