Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, MN, USA.
Division of Hematology-Oncology, Tufts University School of Medicine, Boston, MA, USA.
Leuk Lymphoma. 2021 Nov;62(11):2568-2586. doi: 10.1080/10428194.2021.1927021. Epub 2021 May 17.
Following the observation of interleukin 3 receptor α chain (IL-3Rα; CD123) upregulation on leukemia stem cells (LSCs) almost two decades ago, targeted treatment CD123-diptheria toxin conjugates has now been tested in patients with diverse myeloid malignancies. Targeted eradication of LSCs could result in effective treatments for many challenging diseases initiated by these cells. Consequently, considerable effort has been directed toward targeting CD123 as a potential strategy for treating patients with hematologic malignancies in which CD123 is overexpressed. However, these therapies have had limited success so far, highlighting the need for suitable criteria to identify patients who could benefit from them. Given the diversity in CD123 expression across different hematologic malignancies, understanding CD123 expression patterns and the functional pathogenetic significance is crucial. Here, we review the methodologies available for CD123 assessment and discuss the biological and clinical characteristics of patients for whom CD123-targeting therapies may have a clinical impact.
大约二十年前,人们观察到白血病干细胞(LSCs)上白细胞介素 3 受体 α 链(IL-3Rα;CD123)的上调,此后,针对 CD123-白喉毒素缀合物的靶向治疗已在多种骨髓恶性肿瘤患者中进行了测试。靶向清除 LSCs 可能会为这些细胞引发的许多具有挑战性的疾病提供有效的治疗方法。因此,人们已经投入了相当大的努力来靶向 CD123,将其作为治疗血液系统恶性肿瘤中 CD123 过表达患者的潜在策略。然而,到目前为止,这些疗法的效果有限,这凸显了需要合适的标准来识别可能从中受益的患者。鉴于不同血液系统恶性肿瘤中 CD123 的表达存在多样性,了解 CD123 的表达模式和功能发病机制意义重大。在这里,我们回顾了用于 CD123 评估的方法,并讨论了具有临床影响的 CD123 靶向治疗的患者的生物学和临床特征。