Target intelligence / Profile preview

Chimeric antigen receptor (CD19-directed) (CAR-T cell (CD19-CAR-T cell))

Target
CAR-T cell (CD19-CAR-T cell)
Molecular classification
Receptor (synthetic, genetically engineered), Chimeric antigen receptor, Immune cell receptor
01

Overview

Chimeric antigen receptor T cell therapy utilizes a genetically engineered receptor, commonly with specificity for CD19, to arm a patient’s own cytotoxic T cells against cancer. The CAR construct comprises an extracellular antigen recognition domain (often a single-chain variable fragment targeting CD19), a hinge region, a transmembrane domain, and intracellular signaling/co-stimulatory domains (e.g. CD3ζ, CD28, 4-1BB). When infused back into the patient, these engineered cells selectively bind and eradicate CD19-expressing malignant B cells independently of MHC recognition, often producing durable remissions in relapsed or refractory B-cell malignancies. FDA-approved therapies include tisagenlecleucel and axicabtagene ciloleucel. Severe toxicities such as cytokine release syndrome and neurotoxicity remain key challenges, and ongoing research seeks to improve efficacy, safety, and broaden applications beyond hematologic cancers

Other names
CAR T cellCD19 CAR T cellCD19-directed CAR T cellChimeric antigen receptor-modified T cell (CD19)Genetically engineered CD19-targeted CAR-T cell
02

Mechanism of action

Genetically engineering T cells to express CAR with extracellular single-chain variable fragment (scFv) that binds CD19 antigen, resulting in T cell activation, proliferation, and targeted lysis of CD19-expressing cancer cells

03

Biological functions

Immune responseCell proliferationCell deathSignal transductionTargeted cytotoxicity
04

Disease associations

CancerHematologic malignancies (e.g. acute lymphoblastic leukemia, non-Hodgkin lymphoma, B-cell lymphoma)
05

Safety considerations

Cytokine release syndrome (CRS)Neurotoxicity (immune effector cell-associated neurotoxicity syndrome, ICANS)Prolonged B cell aplasia (leading to increased infection risk)Tumor antigen escape (loss of CD19 target)Limited efficacy in solid tumorsRelapse due to antigen loss or immune evasion
06

Interacting drugs

Tisagenlecleucel (Kymriah)

4 more in the full profile.

07

Biomarkers

CD19 antigen expression on tumor cellsPatient immune statusCytokine profiles (for therapy monitoring and toxicity risk)

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