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AUTO3

Development stage
Phase 2
Lead developer
Autolus Therapeutics
Modality
Gene Addition/Replacement → Gene Therapies, Gene Silencing → Gene Therapies, Gene Editing → Gene Therapies, CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies
Administration
Intravenous
01

Overview

AUTO3 is a bicistronic chimeric antigen receptor (CAR) T-cell therapy developed for the treatment of B-cell malignancies such as acute lymphoblastic leukemia (ALL) and diffuse large B cell lymphoma (DLBCL). It is an autologous cell therapy product that co-expresses two humanized second-generation CARs targeting CD19 and CD22 antigens on B cells. The dual targeting approach aims to minimize relapse due to single antigen loss—a common resistance mechanism in current single-targeted CAR-T therapies. Developed by Autolus in collaboration with University College London, AUTO3 has demonstrated high efficacy and a favorable safety profile in early clinical trials for pediatric ALL and adult DLBCL. The product is manufactured using a bicistronic γ-retroviral vector to transduce patient-derived T cells with both anti-CD19 and anti-CD22 receptors[1][2][6][8].

Other names
autologous anti-CD19/CD22 CAR-T cells AUTO3CD19/22-CAR productsTan-CAR (tandem CAR)cotransduced CAR T cells
02

Targets

CD22 (Cluster of Differentiation 22)CD19 (B lymphocyte antigen CD19)

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