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The Leukemic Microenvironment Represses Blinatumomab-Dependent Killing in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia
Background and aim Blinatumomab is a bispecific T-cell engaging antibody that binds to CD19 on B-cells and CD3 on T-cells, thereby initiating an interaction between these cells and leading to the subsequent lysis of B-cells. Blinatumomab has demonstrated promising results in pediatric B-cell precurs...
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Published in: | Blood 2024-11, Vol.144, p.4228-4228 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | Background and aim
Blinatumomab is a bispecific T-cell engaging antibody that binds to CD19 on B-cells and CD3 on T-cells, thereby initiating an interaction between these cells and leading to the subsequent lysis of B-cells. Blinatumomab has demonstrated promising results in pediatric B-cell precursor acute lymphoblastic leukemia (BCP-ALL) patients. However, not all patients show an initial or lasting response to blinatumomab, and the mechanism behind this is not clearly understood.
T-cells are highly sensitive to modulation by factors such as cytokines and co-stimulatory signals, which can impact T-cell activity, and subsequently the working of blinatumomab. In BCP-ALL, leukemic cells exploit the bone marrow (BM) microenvironment and actively modulate the supportive function of stromal cells, such as mesenchymal stromal cells (MSCs). We showed that this leukemic BM microenvironment is markedly different from its healthy counterpart, facilitates chemotherapy resistance and secretes specific cyto- and chemokines (Polak et al., Blood 2015; Smeets et al, Haematologica 2024). B-ALL-derived MSCs have been observed to suppress T-cell proliferation and reduce pro-inflammatory cytokine secretion (Zanetti et al., JITC 2020). This study aims to identify the effect of the leukemic BM microenvironment on the blinatumomab-dependent killing of BCP-ALL cells.
Results
An ex vivo co-culture of patient derived xenograft (PDX) BCP-ALL cells and pre-activated allogeneic T-cells (with IL-2, IL-7, IL-15) was created with or without patient-derived MSCs. Forty hours after initiation, the co-culture was exposed to 1nM blinatumomab for 48 hours. Cell survival was assessed using flow cytometry. A lower blinatumomab-dependent killing was observed in 3 out of 4 BCP-ALL samples in the presence of MSCs (median reduction of 20.5%), which was independent of T-cell donor (n=2).
Next, BM-derived samples of newly diagnosed pediatric BCP-ALL patients were used to confirm the observed immunosuppressive effect of the leukemic microenvironment. These samples contain both BCP-ALL cells and varying numbers of autologous T-cells that have been exposed to cytokines and chemokines in the leukemic microenvironment of the patient. Nineteen primary BCP-ALL samples were ex vivo exposed to 1 nM blinatumomab for 48 hours. Fourteen (~75%) BCP-ALL samples did not reach a blinatumomab-dependent killing of leukemic cells greater than 45% and were considered ex vivo blinatumomab non-responders. Following CD3/C |
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ISSN: | 0006-4971 |
DOI: | 10.1182/blood-2024-199007 |