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中国临床药理学与治疗学 ›› 2025, Vol. 30 ›› Issue (12): 1711-1721.doi: 10.12092/j.issn.1009-2501.2025.12.015

• 综述与讲座 • 上一篇    下一篇

弥漫性大B细胞淋巴瘤的病理机制及其免疫治疗的研究进展

张箫扬子1,2,祝永福3,梅旦1   

  1. 1皖南医学院第一附属医院(弋矶山医院),皖南医学院脑科学研究院,芜湖  241001,安徽;2沈阳药科大学临床药学院,沈阳  110016,辽宁;3安徽中医药大学第一附属医院肿瘤1科,安徽  230031 合肥

  • 收稿日期:2024-11-07 修回日期:2025-02-06 出版日期:2025-12-26 发布日期:1900-01-01
  • 通讯作者: 梅旦,通信作者,男,博士,助理研究员,研究方向:自身免疫病学及抗炎免疫药理学。 E-mail: meidan225@outlook.com
  • 作者简介:张箫扬子,女,研究方向:临床药学。 E-mail: zxiaoyangzi@163.com
  • 基金资助:
    安徽省教育厅2022年高校科研项目(2022AH050415);皖南医学院弋矶山医院2024年人才引进专项(KY29230709)

Advances in the pathogenesis of diffuse large B-cell lymphoma and its immunotherapy

ZHANGXIAO Yangzi1,2, ZHU Yongfu3, MEI Dan1   

  1. 1The First Affliated Hospital of Wannan Medical College (Yijishan Hospital); Institutes of Brain Science, Wannan Medical College, Wuhu 241001, Anhui, China; 2School of Clinical Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, Liaoning, China; 3Department of Oncology I, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei 230031, Anhui, China
  • Received:2024-11-07 Revised:2025-02-06 Online:2025-12-26 Published:1900-01-01

摘要:

弥漫性大B细胞淋巴瘤(diffuse large B-cell lymphoma,DLBCL)是一种高度异质性和侵袭性的血液恶性肿瘤,因其易复发、难再愈等特点成为临床上亟需解决的难题。肿瘤免疫治疗通过激发或重建机体的免疫系统,识别并消除肿瘤细胞,展现出对DLBCL显著的治疗潜力。从早期的单克隆抗体,到双/多特异性抗体、嵌合抗原受体(chimeric antigen receptor,CAR)疗法,再到近些年出现的溶瘤病毒和基因治疗,免疫治疗技术的持续发展为DLBCL患者提供了更多的治疗选择。随着对DLBCL免疫病理机制和肿瘤微环境的深入研究,新的免疫疗法有望进一步提高治疗效果并改善患者预后。本文就DLBCL的免疫病理机制及其在肿瘤免疫治疗领域的研究进展进行综述。

关键词: 肿瘤免疫治疗, 弥漫性大B细胞淋巴瘤, 肿瘤微环境

Abstract:

Diffuse large B-cell lymphoma (DLBCL) is a highly heterogeneous and aggressive hematologic malignancy that poses significant challenges in clinical practice due to its tendency for relapse and difficulty in achieving lasting remission. Tumor immunotherapy has shown considerable therapeutic potential for DLBCL by stimulating or reconstructing the body's immune system to recognize and eliminate tumor cells. The evolution of immunotherapy, from early monoclonal antibodies to bispecific/multispecific antibodies, chimeric antigen receptor (CAR) therapy, and more recently oncolytic viruses and gene therapies, has provided DLBCL patients with a broader range of treatment options. With ongoing research into the immunopathological mechanisms of DLBCL and its tumor microenvironment, new immunotherapies are expected to further enhance treatment efficacy and improve patient outcomes. This paper reviews the immunopathological mechanisms of DLBCL and the advancements in immunotherapy for this condition.

Key words: cancer immunotherapy, diffuse large B-cell lymphoma, tumor microenvironment

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