Sun Jennifer, Muz Barbara, Alhallak Kinan, Markovic Matea, Gurley Shannon, Wang Zhe, Guenthner Nicole, Wasden Katherine, Fiala Mark, King Justin, Kohnen Daniel, Salama Noha Nabil, Vij Ravi, Azab Abdel Kareem
Department of Radiation Oncology, Cancer Biology Division, Washington University in St. Louis School of Medicine, St. Louis, MO 63108, USA.
Department of Biomedical Engineering, Washington University in St. Louis McKelvey School of Engineering, St. Louis, MO 63130, USA.
Cancers (Basel). 2020 Jan 28;12(2):305. doi: 10.3390/cancers12020305.
Multiple myeloma (MM) remains to be incurable despite recent therapeutic advances. CD47, an immune checkpoint known as the "don't eat me" signal, is highly expressed on the surface of various cancers, allowing cancer cells to send inhibitory signals to macrophages and impede phagocytosis and immune response. In this study, we hypothesized that blocking the "don't eat me" signaling using an anti-CD47 monoclonal antibody will induce killing of MM cells. We report that CD47 expression was directly correlated with stage of the disease, from normal to MGUS to MM. Moreover, MM cells had remarkably higher CD47 expression than other cell populations in the bone marrow. These findings indicate that CD47 is specifically expressed on MM and can be used as a potential therapeutic target. Further, blocking of CD47 using an anti-CD47 antibody induced immediate activation of macrophages, which resulted in induction of phagocytosis and killing of MM cells in the 3D-tissue engineered bone marrow model, as early as 4 hours. These results suggest that macrophage checkpoint immunotherapy by blocking the CD47 "don't eat me" signal is a novel and promising strategy for the treatment of MM, providing a basis for additional studies to validate these effects in vivo and in patients.
尽管近期在治疗方面取得了进展,但多发性骨髓瘤(MM)仍然无法治愈。CD47是一种被称为“别吃我”信号的免疫检查点,在各种癌症表面高度表达,使癌细胞能够向巨噬细胞发送抑制信号,从而阻碍吞噬作用和免疫反应。在本研究中,我们假设使用抗CD47单克隆抗体阻断“别吃我”信号将诱导MM细胞的杀伤。我们报告称,CD47的表达与疾病阶段直接相关,从正常状态到意义未明的单克隆丙种球蛋白病(MGUS)再到MM。此外,MM细胞的CD47表达明显高于骨髓中的其他细胞群体。这些发现表明,CD47在MM上特异性表达,可作为潜在的治疗靶点。此外,使用抗CD47抗体阻断CD47可立即激活巨噬细胞,早在4小时就导致在三维组织工程骨髓模型中诱导吞噬作用并杀伤MM细胞。这些结果表明,通过阻断CD47“别吃我”信号进行巨噬细胞检查点免疫疗法是一种治疗MM的新型且有前景的策略,为在体内和患者中验证这些效果的进一步研究提供了基础。