• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于多发性骨髓瘤免疫治疗的免疫检查点抑制剂

Immune checkpoint inhibitors for multiple myeloma immunotherapy.

作者信息

Liu Zhaoyun, Xu Xintong, Liu Hui, Zhao Xianghong, Yang Chun, Fu Rong

机构信息

Department of Hematology, Tianjin Medical University General Hospital, Tianjin, 300052, China.

出版信息

Exp Hematol Oncol. 2023 Nov 28;12(1):99. doi: 10.1186/s40164-023-00456-5.

DOI:10.1186/s40164-023-00456-5
PMID:38017516
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10685608/
Abstract

Multiple myeloma (MM) is related to immune disorders, recent studys have revealed that immunotherapy can greatly benefit MM patients. Immune checkpoints can negatively modulate the immune system and are closely associated with immune escape. Immune checkpoint-related therapy has attracted much attention and research in MM. However, the efficacy of those therapies need further improvements. There need more thoughts about the immune checkpoint to translate their use in clinical work. In our review, we aggregated the currently known immune checkpoints and their corresponding ligands, further more we propose various ways of potential translation applying treatment based on immune checkpoints for MM patients.

摘要

多发性骨髓瘤(MM)与免疫紊乱有关,最近的研究表明免疫疗法可使MM患者受益匪浅。免疫检查点可对免疫系统产生负调节作用,并与免疫逃逸密切相关。免疫检查点相关疗法在MM领域已引起广泛关注和研究。然而,这些疗法的疗效仍需进一步提高。在将免疫检查点应用于临床工作方面,仍需更多思考。在本综述中,我们汇总了目前已知的免疫检查点及其相应配体,此外,我们还提出了基于免疫检查点对MM患者进行潜在治疗转化的各种方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/4f53c63c8c6f/40164_2023_456_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/34c136c5b208/40164_2023_456_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/fb7223ab7132/40164_2023_456_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/a85e08d4820f/40164_2023_456_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/d704901f54f8/40164_2023_456_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/6e3b234e442b/40164_2023_456_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/678648549653/40164_2023_456_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/4f53c63c8c6f/40164_2023_456_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/34c136c5b208/40164_2023_456_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/fb7223ab7132/40164_2023_456_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/a85e08d4820f/40164_2023_456_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/d704901f54f8/40164_2023_456_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/6e3b234e442b/40164_2023_456_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/678648549653/40164_2023_456_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4529/10685608/4f53c63c8c6f/40164_2023_456_Fig7_HTML.jpg

相似文献

1
Immune checkpoint inhibitors for multiple myeloma immunotherapy.用于多发性骨髓瘤免疫治疗的免疫检查点抑制剂
Exp Hematol Oncol. 2023 Nov 28;12(1):99. doi: 10.1186/s40164-023-00456-5.
2
Inappropriate Expression of PD-1 and CTLA-4 Checkpoints in Myeloma Patients Is More Pronounced at Diagnosis: Implications for Time to Progression and Response to Therapeutic Checkpoint Inhibitors.在骨髓瘤患者中,PD-1 和 CTLA-4 检查点的异常表达在诊断时更为明显:对进展时间和治疗性检查点抑制剂反应的影响。
Int J Mol Sci. 2023 Mar 17;24(6):5730. doi: 10.3390/ijms24065730.
3
V-Set and immunoglobulin domain containing (VSIG) proteins as emerging immune checkpoint targets for cancer immunotherapy.V -set 及免疫球蛋白结构域包含蛋白(VSIG)作为癌症免疫治疗中的新兴免疫检查点靶点。
Front Immunol. 2022 Sep 15;13:938470. doi: 10.3389/fimmu.2022.938470. eCollection 2022.
4
Immune checkpoint inhibitors in multiple myeloma: A review of the literature.多发性骨髓瘤中的免疫检查点抑制剂:文献综述
Pathol Res Pract. 2020 Oct;216(10):153114. doi: 10.1016/j.prp.2020.153114. Epub 2020 Jul 13.
5
NK Cell-Based Immune Checkpoint Inhibition.基于自然杀伤细胞的免疫检查点抑制。
Front Immunol. 2020 Feb 13;11:167. doi: 10.3389/fimmu.2020.00167. eCollection 2020.
6
Deregulated Expression of Immune Checkpoints on Circulating CD4 T Cells May Complicate Clinical Outcome and Response to Treatment with Checkpoint Inhibitors in Multiple Myeloma Patients.循环 CD4 T 细胞上免疫检查点的失调表达可能使多发性骨髓瘤患者的临床结局和对检查点抑制剂治疗的反应复杂化。
Int J Mol Sci. 2021 Aug 27;22(17):9298. doi: 10.3390/ijms22179298.
7
TIGIT and CD96: new checkpoint receptor targets for cancer immunotherapy.TIGIT和CD96:癌症免疫治疗的新型检查点受体靶点
Immunol Rev. 2017 Mar;276(1):112-120. doi: 10.1111/imr.12518.
8
Targeted Therapy of B7 Family Checkpoints as an Innovative Approach to Overcome Cancer Therapy Resistance: A Review from Chemotherapy to Immunotherapy.B7 家族检查点的靶向治疗作为克服癌症治疗耐药性的创新方法:从化疗到免疫治疗的综述。
Molecules. 2022 May 31;27(11):3545. doi: 10.3390/molecules27113545.
9
Targeting Checkpoint Receptors and Molecules for Therapeutic Modulation of Natural Killer Cells.针对免疫检查点受体和分子的自然杀伤细胞治疗调节。
Front Immunol. 2018 Sep 10;9:2041. doi: 10.3389/fimmu.2018.02041. eCollection 2018.
10
Immune Checkpoint Inhibitors in Peripheral T-Cell Lymphoma.外周T细胞淋巴瘤中的免疫检查点抑制剂
Front Pharmacol. 2022 Apr 26;13:869488. doi: 10.3389/fphar.2022.869488. eCollection 2022.

引用本文的文献

1
Recent advances in oncolytic virus combined immunotherapy in tumor treatment.溶瘤病毒联合免疫疗法在肿瘤治疗中的最新进展
Genes Dis. 2025 Mar 12;12(6):101599. doi: 10.1016/j.gendis.2025.101599. eCollection 2025 Nov.
2
Immune Checkpoint Molecules in Hodgkin Lymphoma and Other Hematological Malignancies.霍奇金淋巴瘤及其他血液系统恶性肿瘤中的免疫检查点分子
Cancers (Basel). 2025 Jul 10;17(14):2292. doi: 10.3390/cancers17142292.
3
Altered dynamics of T cell subsets in peripheral blood impacts disease progression in newly diagnosed multiple myeloma.

本文引用的文献

1
PD-1 and LAG-3-positive T cells are associated with clinical outcomes of relapsed/refractory multiple myeloma patients.PD-1 和 LAG-3 阳性 T 细胞与复发/难治性多发性骨髓瘤患者的临床结局相关。
Eur J Med Res. 2022 Dec 19;27(1):296. doi: 10.1186/s40001-022-00923-5.
2
Different expression patterns of VISTA concurrent with PD-1, Tim-3, and TIGIT on T cell subsets in peripheral blood and bone marrow from patients with multiple myeloma.多发性骨髓瘤患者外周血和骨髓中T细胞亚群上VISTA与PD-1、Tim-3和TIGIT的不同表达模式。
Front Oncol. 2022 Nov 10;12:1014904. doi: 10.3389/fonc.2022.1014904. eCollection 2022.
3
外周血中T细胞亚群动力学的改变影响新诊断多发性骨髓瘤的疾病进展。
Biochem Biophys Rep. 2025 Jun 23;43:102104. doi: 10.1016/j.bbrep.2025.102104. eCollection 2025 Sep.
4
Overcoming resistance to immunotherapy by targeting CD38 in human tumor explants.通过靶向人类肿瘤外植体中的CD38克服免疫治疗耐药性。
Cell Rep Med. 2025 Jul 15;6(7):102210. doi: 10.1016/j.xcrm.2025.102210. Epub 2025 Jun 27.
5
Genetic, epigenetic, and molecular determinants of multiple myeloma and precursor plasma cell disorders: a pathophysiological overview.多发性骨髓瘤和前驱浆细胞疾病的遗传、表观遗传及分子决定因素:病理生理学概述
Med Oncol. 2025 Jun 3;42(7):234. doi: 10.1007/s12032-025-02807-0.
6
Monoclonal gammopathy of undetermined significance in patients with solid tumours: Effects of immune checkpoint inhibitors on the monoclonal protein.实体瘤患者意义未明的单克隆丙种球蛋白病:免疫检查点抑制剂对单克隆蛋白的影响
Br J Haematol. 2025 Jun;206(6):1849-1852. doi: 10.1111/bjh.20143. Epub 2025 May 12.
7
Mesenchymal stromal cells in bone marrow niche of patients with multiple myeloma: a double-edged sword.多发性骨髓瘤患者骨髓微环境中的间充质基质细胞:一把双刃剑。
Cancer Cell Int. 2025 Mar 26;25(1):117. doi: 10.1186/s12935-025-03741-x.
8
Antibody-Based Immunotherapies for the Treatment of Hematologic Malignancies.用于治疗血液系统恶性肿瘤的基于抗体的免疫疗法
Cancers (Basel). 2024 Dec 15;16(24):4181. doi: 10.3390/cancers16244181.
9
CD34 and CD34 MM cells show different immune-checkpoint molecule expression profiles: high expression of CD112 and CD137 ligand on CD34 MM cells.CD34阳性和CD34阴性多发性骨髓瘤细胞显示出不同的免疫检查点分子表达谱:CD34阳性多发性骨髓瘤细胞上CD112和CD137配体高表达。
Int J Hematol. 2025 Jan;121(1):89-99. doi: 10.1007/s12185-024-03867-0. Epub 2024 Nov 12.
10
A single-cell transcriptomic map of the murine and human multiple myeloma immune microenvironment across disease stages.单细胞转录组图谱描绘了疾病各阶段的鼠类和人类多发性骨髓瘤免疫微环境。
J Hematol Oncol. 2024 Nov 7;17(1):107. doi: 10.1186/s13045-024-01629-3.
Mitochondrial metabolic determinants of multiple myeloma growth, survival, and therapy efficacy.
多发性骨髓瘤生长、存活及治疗疗效的线粒体代谢决定因素
Front Oncol. 2022 Sep 16;12:1000106. doi: 10.3389/fonc.2022.1000106. eCollection 2022.
4
Adenosinergic axis and immune checkpoint combination therapy in tumor: A new perspective for immunotherapy strategy.腺苷能轴与免疫检查点联合治疗肿瘤:免疫治疗策略的新视角。
Front Immunol. 2022 Sep 8;13:978377. doi: 10.3389/fimmu.2022.978377. eCollection 2022.
5
Elraglusib (9-ING-41), a selective small-molecule inhibitor of glycogen synthase kinase-3 beta, reduces expression of immune checkpoint molecules PD-1, TIGIT and LAG-3 and enhances CD8 T cell cytolytic killing of melanoma cells.Elraglusib(9-ING-41)是一种选择性的糖原合酶激酶-3β小分子抑制剂,可降低免疫检查点分子 PD-1、TIGIT 和 LAG-3 的表达,并增强 CD8 T 细胞对黑色素瘤细胞的细胞溶解杀伤作用。
J Hematol Oncol. 2022 Sep 14;15(1):134. doi: 10.1186/s13045-022-01352-x.
6
Targeting the CD47-SIRPα Innate Immune Checkpoint to Potentiate Antibody Therapy in Cancer by Neutrophils.靶向CD47-SIRPα天然免疫检查点以增强中性粒细胞在癌症中的抗体治疗作用。
Cancers (Basel). 2022 Jul 11;14(14):3366. doi: 10.3390/cancers14143366.
7
CD155/TIGIT signalling plays a vital role in the regulation of bone marrow mesenchymal stem cell-induced natural killer-cell exhaustion in multiple myeloma.CD155/TIGIT信号传导在多发性骨髓瘤中骨髓间充质干细胞诱导的自然杀伤细胞耗竭的调节中起着至关重要的作用。
Clin Transl Med. 2022 Jul;12(7):e861. doi: 10.1002/ctm2.861.
8
Tim-3 Blockade Elicits Potent Anti-Multiple Myeloma Immunity of Natural Killer Cells.Tim-3阻断可引发自然杀伤细胞强大的抗多发性骨髓瘤免疫反应。
Front Oncol. 2022 Feb 25;12:739976. doi: 10.3389/fonc.2022.739976. eCollection 2022.
9
Checkpoint Inhibitors in Multiple Myeloma: Intriguing Potential and Unfulfilled Promises.多发性骨髓瘤中的检查点抑制剂:诱人的潜力与未实现的承诺
Cancers (Basel). 2021 Dec 27;14(1):113. doi: 10.3390/cancers14010113.
10
Carfilzomib modulates tumor microenvironment to potentiate immune checkpoint therapy for cancer.卡非佐米调节肿瘤微环境以增强癌症的免疫检查点治疗。
EMBO Mol Med. 2022 Jan 11;14(1):e14502. doi: 10.15252/emmm.202114502. Epub 2021 Dec 13.