Investigators reported that monotherapy using base-edited “universal” donor CAR T cells against CD33, CLL-1, or CD7 delivered inhibition of acute myeloid leukaemia in immunodeficient mice when antigen expression was homogenous. Still, the combined use of BE-CAR33 and BE-CARCLL-1 T cells was required to address heterogeneous CLL-1-/+CD33-/+ disease.
[Leukemia]

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