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The role of PD-1 and PD-L1 in T-cell immune suppression in patients with hematological malignancies

机译:PD-1和PD-L1在血液系统恶性肿瘤患者T细胞免疫抑制中的作用

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T-cell activation and dysfunction relies on direct and modulated receptors. Based on their functional outcome, co-signaling molecules can be divided as co-stimulators and co-inhibitors, which positively and negatively control the priming, growth, differentiation and functional maturation of a T-cell response. We are beginning to understand the power of co-inhibitors in the context of lymphocyte homeostasis and the pathogenesis of leukemia, which involves several newly described co-inhibitory pathways, including the programmed death-1 (PD-1) and PD-1 ligand (PD-L1) pathway. The aim of this review is to summarize the PD-1 and PD-L1 biological functions and their alterative expression in hematological malignancies. The role of PD-1 and PD-L1 in T-cell immune suppression and the potential for immunotherapy via blocking PD-1 and PD-L1 in hematological malignancies are also reviewed.
机译:T细胞活化和功能障碍依赖于直接和调节的受体。基于它们的功能结果,共信号分子可分为共刺激剂和共抑制剂,它们积极和消极地控制T细胞反应的引发,生长,分化和功能成熟。我们开始了解在淋巴细胞稳态和白血病发病机制中共抑制剂的作用,其中涉及几种新描述的共抑制途径,包括程序性死亡1(PD-1)和PD-1配体( PD-L1)途径。这篇综述的目的是总结PD-1和PD-L1的生物学功能及其在血液系统恶性肿瘤中的替代表达。还综述了PD-1和PD-L1在T细胞免疫抑制中的作用以及通过阻断PD-1和PD-L1在血液系统恶性肿瘤中进行免疫治疗的潜力。

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