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Universal CLL1 CAR-T cells are an allogeneic, "off-the-shelf" chimeric antigen receptor (CAR) T-cell therapy designed to target C-type lectin-like molecule 1 (CLL-1, also known as CLEC12A). Developed by Mingfeng Zhao at Tianjin First Central Hospital, these cells are engineered using a specialized non-gene editing intracellular membrane protein retention technology. This platform allows for the creation of universal CAR-T cells without the need for traditional gene-editing tools like CRISPR/Cas9 to prevent Graft-versus-Host Disease (GvHD) and immune rejection. CLL-1 is a highly attractive target for acute myeloid leukemia (AML) as it is expressed on over 90% of AML blasts and leukemic stem cells (LSCs) while being absent on normal hematopoietic stem cells, potentially allowing for the eradication of the disease while sparing healthy bone marrow function.
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