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靶向CD47作为多发性骨髓瘤的新型免疫疗法

Targeting CD47 as a Novel Immunotherapy for Multiple Myeloma.

作者信息

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

机构信息

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.

出版信息

Cancers (Basel). 2020 Jan 28;12(2):305. doi: 10.3390/cancers12020305.

DOI:10.3390/cancers12020305
PMID:32012878
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7072283/
Abstract

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.

摘要

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。

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Pembrolizumab plus pomalidomide and dexamethasone for patients with relapsed or refractory multiple myeloma (KEYNOTE-183): a randomised, open-label, phase 3 trial.帕博利珠单抗联合泊马度胺和地塞米松治疗复发或难治性多发性骨髓瘤患者(KEYNOTE-183):一项随机、开放标签的3期试验。
Lancet Haematol. 2019 Sep;6(9):e459-e469. doi: 10.1016/S2352-3026(19)30110-3. Epub 2019 Jul 18.
2
Engineering macrophages to phagocytose cancer cells by blocking the CD47/SIRPɑ axis.通过阻断 CD47/SIRPɑ 轴工程化巨噬细胞吞噬癌细胞。
Cancer Med. 2019 Aug;8(9):4245-4253. doi: 10.1002/cam4.2332. Epub 2019 Jun 11.
3
Targeting CD47 as a cancer therapeutic strategy: the cutaneous T-cell lymphoma experience.
Front Immunol. 2025 Jul 18;16:1613265. doi: 10.3389/fimmu.2025.1613265. eCollection 2025.
4
SIRPα blockade therapy potentiates immunotherapy by inhibiting PD-L1 myeloid cells in hepatocellular carcinoma.信号调节蛋白α(SIRPα)阻断疗法通过抑制肝细胞癌中程序性死亡配体1(PD-L1)髓系细胞来增强免疫疗法。
Cell Death Dis. 2025 Jun 16;16(1):451. doi: 10.1038/s41419-025-07779-7.
5
Final Results of a Phase 2 Multi-Arm Study of Magrolimab Combinations in Patients With Relapsed/Refractory Multiple Myeloma.复发/难治性多发性骨髓瘤患者中玛格罗利单抗联合用药的2期多臂研究最终结果
EJHaem. 2025 Jun 6;6(3):e70072. doi: 10.1002/jha2.70072. eCollection 2025 Jun.
6
Monoclonal anti-CD38 therapy in human myeloma: retrospects and prospects.人骨髓瘤中的单克隆抗CD38疗法:回顾与展望。
Front Immunol. 2025 Feb 12;16:1519300. doi: 10.3389/fimmu.2025.1519300. eCollection 2025.
7
Cell surface marker heterogeneity in human myeloma cell lines for modeling of disease and therapy.人骨髓瘤细胞系中细胞表面标志物的异质性,用于疾病建模和治疗。
Sci Rep. 2024 Nov 20;14(1):28805. doi: 10.1038/s41598-024-80263-y.
8
DNp73 enhances tumor progression and immune evasion in multiple myeloma by targeting the MYC and MYCN pathways.DNp73 通过靶向 MYC 和 MYCN 通路增强多发性骨髓瘤的肿瘤进展和免疫逃逸。
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9
IL-10R inhibition reprograms tumor-associated macrophages and reverses drug resistance in multiple myeloma.白细胞介素-10 受体抑制作用可重塑肿瘤相关巨噬细胞,并逆转多发性骨髓瘤的耐药性。
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10
Deciphering the role of CD47 in cancer immunotherapy.解析 CD47 在癌症免疫疗法中的作用。
J Adv Res. 2024 Sep;63:129-158. doi: 10.1016/j.jare.2023.10.009. Epub 2023 Oct 28.
以 CD47 为靶点的癌症治疗策略:皮肤 T 细胞淋巴瘤的经验。
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4
The Phagocytic Function of Macrophage-Enforcing Innate Immunity and Tissue Homeostasis.巨噬细胞的吞噬功能——先天免疫与组织动态平衡的执行者。
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5
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Eur J Cancer. 2017 May;76:100-109. doi: 10.1016/j.ejca.2017.02.013. Epub 2017 Mar 10.
6
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Lancet Oncol. 2017 Mar;18(3):312-322. doi: 10.1016/S1470-2045(17)30065-7. Epub 2017 Jan 26.
7
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J Hematol Oncol. 2016 Nov 3;9(1):116. doi: 10.1186/s13045-016-0345-3.
8
Nivolumab in Patients With Relapsed or Refractory Hematologic Malignancy: Preliminary Results of a Phase Ib Study.纳武利尤单抗治疗复发或难治性血液系统恶性肿瘤患者:Ib期研究的初步结果
J Clin Oncol. 2016 Aug 10;34(23):2698-704. doi: 10.1200/JCO.2015.65.9789. Epub 2016 Jun 6.
9
Newly established myeloma-derived stromal cell line MSP-1 supports multiple myeloma proliferation, migration, and adhesion and induces drug resistance more than normal-derived stroma.新建立的骨髓瘤来源的基质细胞系MSP-1比正常来源的基质更能支持多发性骨髓瘤的增殖、迁移和黏附,并诱导耐药性。
Haematologica. 2016 Jul;101(7):e307-11. doi: 10.3324/haematol.2016.142190. Epub 2016 Apr 14.
10
A CD138-independent strategy to detect minimal residual disease and circulating tumour cells in multiple myeloma.一种不依赖CD138检测多发性骨髓瘤微小残留病和循环肿瘤细胞的策略。
Br J Haematol. 2016 Apr;173(1):70-81. doi: 10.1111/bjh.13927. Epub 2016 Jan 5.