Targeting CD47-SIRPα axis for Hodgkin and non-Hodgkin lymphoma immunotherapy.

Targeting CD47-SIRPα axis for Hodgkin and non-Hodgkin lymphoma immunotherapy.
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DOI:
10.1016/j.gendis.2022.12.008
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发表时间:
2024-01
期刊:
影响因子:
6.8
通讯作者:
Wang, Ping
Wang, Ping
中科院分区:
医学2区
文献类型:
--
作者:
Zhao, Pengcheng;Xie, Longyan;Yu, Lei;Wang, Ping

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分化簇47(CD 47)和信号调节蛋白α(SIRPα)之间的相互作用保护健康细胞免受巨噬细胞的攻击,这对于维持免疫稳态至关重要。CD 47的过表达广泛存在于各种肿瘤细胞类型中,并将“不要吃我”信号传递给巨噬细胞,以通过与SIRPα结合来避免吞噬作用。因此,阻断CD 47-SIRPα轴是一种有前途的癌症治疗方法。淋巴瘤是最常见的血液恶性肿瘤,是一个未满足的临床需求的领域。本文主要介绍了目前针对CD 47-SIRPα轴的治疗策略,包括抗体、SIRPα Fc融合蛋白、小分子抑制剂和多肽等在霍奇金淋巴瘤和非霍奇金淋巴瘤的临床前研究和临床试验中的应用。
The interaction between cluster of differentiation 47 (CD47) and signal regulatory protein α (SIRPα) protects healthy cells from macrophage attack, which is crucial for maintaining immune homeostasis. Overexpression of CD47 occurs widely across various tumor cell types and transmits the “don't eat me” signal to macrophages to avoid phagocytosis through binding to SIRPα. Blockade of the CD47-SIRPα axis is therefore a promising approach for cancer treatment. Lymphoma is the most common hematological malignancy and is an area of unmet clinical need. This review mainly described the current strategies targeting the CD47-SIRPα axis, including antibodies, SIRPα Fc fusion proteins, small molecule inhibitors, and peptides both in preclinical studies and clinical trials with Hodgkin lymphoma and non-Hodgkin lymphoma.
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