Christian Kellner

CD19‐directed immunotherapy has become a cornerstone in the therapy of B‐cell precursor acute lymphoblastic leukemia (BCP‐ALL). CD19‐directed cellular and antibody‐based therapeutics have entered therapy of primary and relapsed disease and contributed to improved outcomes in relapsed disease and lower therapy toxicity. However, efficacy remains limited in many cases due to a lack of therapy response, short remission phases, or antigen escape. Here, BCP‐ALL cell lines, patient‐derived xenograft (PDX) samples, human macrophages, and an in vivo transplantation model in NOD.Cg‐Prkdc scid Il2rg tm1Wjl /SzJ (NSG) mice were used to examine the therapeutic potency of a CD19 antibody Fc‐engineered for improved effector cell recruitment (CD19‐DE) and antibody‐dependent cellular phagocytosis (ADCP), in combination with a novel modified CD47 antibody (Hu5F9‐IgG2σ). For the in vivo model, only samples refractory to CD19‐DE monotherapy were chosen. Hu5F9‐IgG2σ enhanced ADCP by CD19‐DE in various BCP‐ALL cell line models with varying CD19 surface expression and cytogenetic backgrounds, two of which contained the KMT2A‐AFF1 fusion. Also, the antibody combination was efficient in inducing ADCP by human macrophages in pediatric PDX samples with and adult samples with and without KMT2A ‐rearrangement in vitro. In a randomized phase 2‐like PDX trial using seven KMT2A ‐rearranged BCP‐ALL samples in NSG mice, the CD19/CD47 antibody combination proved highly efficient. Our findings support that the efficacy of Fc‐engineered CD19 antibodies may be substantially enhanced by a combination with CD47 blockade. This suggests that the combination may be a promising therapy option for BCP‐ALL, especially in relapsed patients and/or patients refractory to CD19‐directed therapy.