Drug intelligence / Profile preview

CD19-CD28 chimeric antigen receptor T cells

Development stage
Phase 1
Lead developer
Baylor College of Medicine
Modality
CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies, Gene Therapies
Administration
Intravenous
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Overview

CD19-CD28 chimeric antigen receptor T cells (also known as CD19.28.z CAR-T cells) are an investigational autologous cell therapy developed by Baylor College of Medicine for the treatment of B-cell malignancies, specifically non-Hodgkin lymphoma (NHL) and chronic lymphocytic leukemia (CLL). The therapy involves genetically modifying a patient's own T cells to express a second-generation chimeric antigen receptor (CAR). This CAR consists of an extracellular single-chain variable fragment (scFv) derived from an anti-CD19 antibody, a CD28 transmembrane and costimulatory domain, and a CD3-zeta intracellular signaling domain. Upon re-infusion, these engineered T cells recognize and bind to the CD19 antigen on the surface of malignant B cells, triggering T-cell activation, proliferation, and targeted cytotoxicity. In the ATECRAB clinical trial context, these cells were evaluated to determine safety and efficacy, often in comparison with EBV-specific T cells modified with the same CAR construct to explore the impact of viral-specific memory on CAR-T persistence.

Other names
CD19-CD28 CAR-T cellsCD-19-CD28 CAR-T cellsCD 19-CD28 CAR-T cellsCD19-CD28 CAR T-cellsCD-19-CD28 CAR T-cellsCD 19-CD28 CAR T-cellsCD19-CD28 chimeric receptor T cellsCD-19-CD28 chimeric receptor T cellsCD 19-CD28 chimeric receptor T cells
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Targets

CD28 (Cluster of Differentiation 28)CD19 (B lymphocyte antigen CD19)CD3 (T-cell surface glycoprotein CD3)

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