Chimeric antigen receptor (CAR) T cell therapy has fundamentally transformed clinical outcomes in B cell malignancies; however, the success story of CAR T cells has not yet extended to T cell acute lymphoblastic leukemia (T-ALL). A primary issue lies in the fundamental biology of the disease; most target antigens are shared between malignant T-ALL blasts and healthy T lymphocytes, including the CAR T cell product itself.
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Kuznetsova et al. (2026) studied this question.
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