Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN; Program in Cancer Biology.
Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN.
Haematologica. 2024 Jul 1;109(7):2111-2121. doi: 10.3324/haematol.2023.283850.
CD47-SIRPa is a myeloid check point pathway that promotes phagocytosis of cells lacking markers for self-recognition. Tumor cells can overexpress CD47 and bind to SIRPa on macrophages, preventing phagocytosis. CD47 expression is enhanced and correlated with a negative prognosis in acute myeloid leukemia (AML), with its blockade leading to cell clearance. ALX90 is an engineered fusion protein with high affinity for CD47. Composed of the N-terminal D1 domain of SIRPα genetically linked to an inactive Fc domain from human immunoglobulin (Ig) G, ALX90 is designed to avoid potential toxicity of CD47-expressing red blood cells. Venetoclax (VEN) is a specific B-cell lymphoma-2 (BCL-2) inhibitor that can restore apoptosis in malignant cells. In AML, VEN is combined with azanucleosides to induce superior remission rates, however treatment for refractory/relapse is an unmet need. We questioned whether the anti-tumor activity of a VENbased regimen can be augmented through CD47 inhibition (CD47i) in AML and how this triplet may be enhanced. Human AML cell lines were sensitive to ALX90 and its addition increased efficacy of a VEN plus azacitidin (VEN+AZA) regimen in vivo. However, CD47i failed to clear bone marrow tumor burden in PDX models. We hypothesized that the loss of resident macrophages in the bone marrow in AML reduced efficiency of CD47i. Therefore, we attempted to enhance this medullary macrophage population with agonism of TLR3 via polyinosinic:polycytidylic acid (poly(I:C)), which led to expansion and activation of medullary macrophages in in vivo AML PDX models and potentiated CD47i. In summary, the addition of poly(I:C) can enhance medullary macrophage populations to potentiate the phagocytosis merited by therapeutic inhibition of CD47.
CD47-SIRPa 是一种髓系检查点通路,可促进缺乏自我识别标记的细胞的吞噬作用。肿瘤细胞可过表达 CD47,并与巨噬细胞上的 SIRPa 结合,从而阻止吞噬作用。CD47 的表达在急性髓细胞白血病 (AML) 中增强,并与不良预后相关,其阻断可导致细胞清除。ALX90 是一种与 CD47 具有高亲和力的工程融合蛋白。它由 SIRPα 的 N 端 D1 结构域组成,通过基因与来自人免疫球蛋白 (Ig) G 的无活性 Fc 结构域相连,旨在避免表达 CD47 的红细胞的潜在毒性。Venetoclax (VEN) 是一种特异性 B 细胞淋巴瘤-2 (BCL-2) 抑制剂,可恢复恶性细胞中的细胞凋亡。在 AML 中,VEN 与氮杂核苷联合使用可诱导更高的缓解率,但对难治性/复发的治疗仍存在未满足的需求。我们质疑在 AML 中通过 CD47 抑制 (CD47i) 是否可以增强 VEN 为基础的治疗方案的抗肿瘤活性,以及如何增强这种三联疗法。人 AML 细胞系对 ALX90 敏感,其添加可增强 VEN 联合阿扎胞苷 (VEN+AZA) 方案在体内的疗效。然而,CD47i 未能清除 PDX 模型中的骨髓肿瘤负担。我们假设 AML 中骨髓中常驻巨噬细胞的丧失降低了 CD47i 的效率。因此,我们试图通过聚肌苷酸:聚胞苷酸 (poly(I:C)) 激动 TLR3 来增强这种骨髓巨噬细胞群体,这导致体内 AML PDX 模型中骨髓巨噬细胞的扩增和激活,并增强了 CD47i。总之,添加 poly(I:C) 可以增强骨髓巨噬细胞群体,从而增强 CD47 治疗性抑制所必需的吞噬作用。