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PD-1/PD-L1/2通路在多发性骨髓瘤中的研究进展
引用本文:马银娟,杨夏影,王莹,王璇,潘耀柱. PD-1/PD-L1/2通路在多发性骨髓瘤中的研究进展[J]. 肿瘤防治研究, 2021, 48(6): 647-651. DOI: 10.3971/j.issn.1000-8578.2021.21.0108
作者姓名:马银娟  杨夏影  王莹  王璇  潘耀柱
作者单位:1. 730050 兰州,中国人民解放军联勤保障部队第九四〇医院血液科;2. 750004 银川,宁夏医科大学研究生院
基金项目:甘肃省卫生行业科研计划项目(GSWSKY-2019-63);军队后勤应用基础研究项目(CLB19J047)
摘    要:多发性骨髓瘤(MM)是一种浆细胞恶性克隆增殖性疾病,近年来,蛋白酶体抑制剂、免疫调节剂在多发性骨髓瘤中的应用明显延长了患者的生存期并提高了生存质量,但因疾病的异质性、易复发及耐药性,目前仍无法治愈。免疫检查点抑制剂如Pembrolizumab、Nivolumab、Pidilizumab、Atezolizumab及Durvalumab等为MM带来了曙光。本文通过回顾近年来国内外的相关文献,综述MM的免疫发病机制、PD-1/PD-L1/2相关的免疫通路及免疫治疗的现状,希望为MM的免疫治疗提供参考。

关 键 词:多发性骨髓瘤  PD-1  PD-L1  PPD-L2  免疫检查点抑制剂  
收稿时间:2021-01-27

Research Progress of PD-1/PD-L1/2 Pathway in Multiple Myeloma
MA Yinjuan,YANG Xiaying,WANG Ying,WANG Xuan,PAN Yaozhu. Research Progress of PD-1/PD-L1/2 Pathway in Multiple Myeloma[J]. Cancer Research on Prevention and Treatment, 2021, 48(6): 647-651. DOI: 10.3971/j.issn.1000-8578.2021.21.0108
Authors:MA Yinjuan  YANG Xiaying  WANG Ying  WANG Xuan  PAN Yaozhu
Affiliation:1. Department of Hematology, The 940th Hospital of Joint Support Force of Chinese People’s Liberation Army, Lanzhou 730050, China; 2. Graduate School of Ningxia Medical University, Yinchuan 750004, China
Abstract:Multiple myeloma is a type of hematological malignancy caused by clonal plasma cell proliferation. In recent years, the application of proteasome inhibitors and immune drugs (IMiDs) in multiple myeloma has prolonged the survival period of patients and improved the quality of life. However, due to the heterogeneity, recurrence and drug resistance of the disease, MM is still incurable. Relatively good response rates of immune checkpoint inhibitors such as Pembrolizumab, Nivolumab, Pidilizumab, Atezolizumab and Durvalumab offer MM a new hope. This article reviews the relevant literature in recent years, introduces the immune pathogenesis of MM, PD-1/PD-L1/2-related immune pathway and the current status of immunotherapy, to provide reference for the immunotherapy of MM.
Keywords:Gansu Province Health Industry Research Project (No. GSWSKY-2019-63)  Grant-in-aid from the PLA Logistics Research Project (No. CLB19J047)  
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