Drug intelligence / Profile preview

TAA-T

Development stage
Phase 1
Lead developer
Children's National Research Institute
Modality
TCR-Engineered T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies, Tumor-Infiltrating Lymphocytes (TILs) → Native Immune Cells → Adoptive Cell Transfer → Cell Therapies, CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies
Administration
Intravenous
01

Overview

TAA-T is an autologous or allogeneic T-cell immunotherapy developed by the Children's National Research Institute for the treatment of relapsed or refractory solid tumors. The therapy consists of ex vivo expanded cytotoxic T lymphocytes (CTLs) specifically trained to target three tumor-associated antigens (TAAs): Wilms tumor protein (WT1), melanoma antigen preferentially expressed in tumors (PRAME), and survivin (BIRC5). Unlike CAR-T therapies that use genetic modification, TAA-T products are generated by stimulating a patient's (autologous) or a donor's (allogeneic/HLA-matched) peripheral blood mononuclear cells with antigen-presenting cells pulsed with pepmixes covering the target antigens. This approach aims to provide a broad anti-tumor response while minimizing off-target toxicity. In Phase I trials, the therapy has demonstrated safety and signs of clinical activity, including disease stabilization and progression-free survival in pediatric and adult patients with high-risk solid tumors.

Other names
Tumor-associated antigen-specific T cellsMulti-tumor associated antigen-specific T cellsMulti-TAA-specific T cellsTumor-associated antigen-specific cytotoxic T lymphocytes
02

Targets

PRAME (Preferentially expressed antigen in melanoma)Survivin-derived peptide–Major Histocompatibility Complex (Survivin-MHC)WT1-pMHC (Wilms Tumor 1-derived peptide–Major Histocompatibility Complex)

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