Drug intelligence / Profile preview

leukemia-specific T cells

Development stage
Unknown
Lead developer
Baylor College of Medicine
Modality
CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies, TCR-Engineered T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies, Tumor-Infiltrating Lymphocytes (TILs) → Native Immune Cells → Adoptive Cell Transfer → Cell Therapies
Administration
Intravenous
01

Overview

Leukemia-specific T cells, also known as mLSTs, are a cell therapy developed by Baylor College of Medicine. These are stem cell donor-derived T cells that are selectively activated and expanded to react to multiple antigens expressed by acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) cells, specifically PRAME, WT1, Survivin, and NY-ESO-1. The therapy is designed to selectively recognize and kill leukemia antigen-pulsed cells without activity against normal cells, thereby enhancing the graft-versus-leukemia (GVL) effect while minimizing graft-versus-host disease (GVHD). It is being investigated for the prevention and treatment of AML and MDS after allogeneic hematopoietic stem cell transplantation (HCT).

Other names
multiple leukemia antigen-specific T cellsstem cell donor–derived multiple leukemia antigen–specific T cells
02

Targets

WT1 (Wilms tumor protein)BIRC5 (Survivin)PRAME (Preferentially expressed antigen in melanoma)

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