• 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

两例B细胞恶性肿瘤患者接受嵌合抗原受体T细胞(CAR-T)治疗后谱系定义抗原完全丧失。

Complete loss of lineage defining antigens in two cases of B-cell malignancies following CAR-T therapy.

作者信息

Torabi Alireza, Love Jason, Hyun Teresa, Pham Angie, Gauthier Jordan, Hirayama Alexandre, Wu David, Naresh Kikkeri

机构信息

Department of Laboratory Medicine and Pathology, University of Washington, Seattle 1959 NE Pacific Street, Box 357110, Seattle, WA, 98195, USA.

Department of Hematopathology, Fred Hutch Cancer Center, Seattle, WA, USA.

出版信息

J Hematop. 2024 Dec;17(4):259-264. doi: 10.1007/s12308-024-00602-w. Epub 2024 Aug 26.

DOI:10.1007/s12308-024-00602-w
PMID:39186243
Abstract

Targeted immunotherapy is a promising approach in treating high-risk and refractory/relapsed lymphoid malignancies. Although this strategy has shown a significant success in treating non-Hodgkin B-cell lymphomas and plasma cell myeloma, relapse with loss of targeted antigen can occur. Rarely, complete loss of multiple lineage specific markers can happen. We are describing 2 cases of B-cell neoplasms along with contributing immunohistochemistry, cytogenetic, and molecular results. Post-targeted CAR-T therapy, both cases, one aggressive B-cell lymphoma and the other plasma cell myeloma, lost B-cell, and plasma cell antigens, respectively. Complete loss of lineage specific markers post-targeted therapy is a rare event that makes the diagnosis of the relapsed neoplasm challenging. In this article, we also reviewed the literature and highlighted possible mechanisms of antigen loss following targeted therapy.

摘要

靶向免疫疗法是治疗高危及难治性/复发性淋巴系统恶性肿瘤的一种很有前景的方法。尽管该策略在治疗非霍奇金B细胞淋巴瘤和浆细胞骨髓瘤方面已取得显著成功,但仍可能出现靶向抗原丢失导致的复发。极少数情况下,会发生多种谱系特异性标志物的完全丢失。我们在此描述2例B细胞肿瘤病例,并给出相关的免疫组织化学、细胞遗传学和分子学结果。在靶向CAR-T治疗后,这两例病例,一例侵袭性B细胞淋巴瘤和另一例浆细胞骨髓瘤,分别失去了B细胞和浆细胞抗原。靶向治疗后谱系特异性标志物的完全丢失是一种罕见事件,这使得复发肿瘤的诊断具有挑战性。在本文中,我们还回顾了文献并强调了靶向治疗后抗原丢失的可能机制。

相似文献

1
Complete loss of lineage defining antigens in two cases of B-cell malignancies following CAR-T therapy.两例B细胞恶性肿瘤患者接受嵌合抗原受体T细胞(CAR-T)治疗后谱系定义抗原完全丧失。
J Hematop. 2024 Dec;17(4):259-264. doi: 10.1007/s12308-024-00602-w. Epub 2024 Aug 26.
2
Efficacy and toxicity for CD22/CD19 chimeric antigen receptor T-cell therapy in patients with relapsed/refractory aggressive B-cell lymphoma involving the gastrointestinal tract.CD22/CD19 嵌合抗原受体 T 细胞疗法治疗累及胃肠道的复发/难治性侵袭性 B 细胞淋巴瘤患者的疗效和毒性。
Cytotherapy. 2020 Mar;22(3):166-171. doi: 10.1016/j.jcyt.2020.01.008. Epub 2020 Feb 13.
3
Anti-CD37 chimeric antigen receptor T cells are active against B- and T-cell lymphomas.抗 CD37 嵌合抗原受体 T 细胞对 B 细胞和 T 细胞淋巴瘤有效。
Blood. 2018 Oct 4;132(14):1495-1506. doi: 10.1182/blood-2018-04-842708. Epub 2018 Aug 8.
4
Current advances in chimeric antigen receptor T-cell therapy for refractory/relapsed multiple myeloma.嵌合抗原受体 T 细胞疗法治疗难治/复发性多发性骨髓瘤的最新进展。
J Zhejiang Univ Sci B. 2020;21(1):29-41. doi: 10.1631/jzus.B1900351.
5
Phase I Trial of Fourth-Generation Anti-CD19 Chimeric Antigen Receptor T Cells Against Relapsed or Refractory B Cell Non-Hodgkin Lymphomas.第四代抗 CD19 嵌合抗原受体 T 细胞治疗复发/难治性 B 细胞非霍奇金淋巴瘤的 I 期临床试验。
Front Immunol. 2020 Nov 27;11:564099. doi: 10.3389/fimmu.2020.564099. eCollection 2020.
6
Chimeric antigen receptor T-cell therapy for the treatment of aggressive B-cell non-Hodgkin lymphomas: efficacy, toxicity, and comparative chimeric antigen receptor products.嵌合抗原受体 T 细胞疗法治疗侵袭性 B 细胞非霍奇金淋巴瘤:疗效、毒性和比较嵌合抗原受体产品。
Expert Opin Biol Ther. 2019 Nov;19(11):1157-1164. doi: 10.1080/14712598.2019.1644316. Epub 2019 Jul 25.
7
Chimeric Antigen Receptor T-Cell Therapies for Aggressive B-Cell Lymphomas: Current and Future State of the Art.用于侵袭性B细胞淋巴瘤的嵌合抗原受体T细胞疗法:当前与未来的技术水平
Am Soc Clin Oncol Educ Book. 2019 Jan;39:446-453. doi: 10.1200/EDBK_238693. Epub 2019 May 17.
8
Pembrolizumab for B-cell lymphomas relapsing after or refractory to CD19-directed CAR T-cell therapy.帕博利珠单抗治疗 CD19 靶向 CAR T 细胞治疗后复发或难治的 B 细胞淋巴瘤。
Blood. 2022 Feb 17;139(7):1026-1038. doi: 10.1182/blood.2021012634.
9
Bispecific anti-CD20, anti-CD19 CAR T cells for relapsed B cell malignancies: a phase 1 dose escalation and expansion trial.双特异性抗 CD20、抗 CD19 CAR T 细胞治疗复发 B 细胞恶性肿瘤:1 期剂量递增和扩展试验。
Nat Med. 2020 Oct;26(10):1569-1575. doi: 10.1038/s41591-020-1081-3. Epub 2020 Oct 5.
10
Exploratory trial of a biepitopic CAR T-targeting B cell maturation antigen in relapsed/refractory multiple myeloma.双表位 CAR T 靶向 B 细胞成熟抗原治疗复发/难治性多发性骨髓瘤的探索性试验。
Proc Natl Acad Sci U S A. 2019 May 7;116(19):9543-9551. doi: 10.1073/pnas.1819745116. Epub 2019 Apr 15.

本文引用的文献

1
BCMA loss in the epoch of novel immunotherapy for multiple myeloma: from biology to clinical practice.BCMA 缺失在多发性骨髓瘤新型免疫治疗时代:从生物学到临床实践。
Haematologica. 2023 Apr 1;108(4):958-968. doi: 10.3324/haematol.2020.266841.
2
Resistance of B-Cell Lymphomas to CAR T-Cell Therapy Is Associated With Genomic Tumor Changes Which Can Result in Transdifferentiation.B细胞淋巴瘤对嵌合抗原受体T细胞(CAR T细胞)疗法的耐药性与可导致转分化的基因组肿瘤变化相关。
Am J Surg Pathol. 2022 Jun 1;46(6):742-753. doi: 10.1097/PAS.0000000000001834. Epub 2021 Nov 18.
3
Hypermethylation of CD19 promoter enables antigen-negative escape to CART-19 in vivo and in vitro.
CD19 启动子的超甲基化使得 CART-19 在体内和体外逃避抗原阴性。
J Immunother Cancer. 2021 Aug;9(8). doi: 10.1136/jitc-2021-002352.
4
Homozygous BCMA gene deletion in response to anti-BCMA CAR T cells in a patient with multiple myeloma.一名多发性骨髓瘤患者中,针对抗BCMA嵌合抗原受体T细胞的纯合BCMA基因缺失。
Nat Med. 2021 Apr;27(4):616-619. doi: 10.1038/s41591-021-01245-5. Epub 2021 Feb 22.
5
Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myeloma.双等位基因 BCMA 缺失导致多发性骨髓瘤患者对 CAR T 细胞治疗产生耐药。
Nat Commun. 2021 Feb 8;12(1):868. doi: 10.1038/s41467-021-21177-5.
6
Standard-of-Care Axicabtagene Ciloleucel for Relapsed or Refractory Large B-Cell Lymphoma: Results From the US Lymphoma CAR T Consortium.阿基仑赛用于复发或难治性大 B 细胞淋巴瘤的标准治疗:来自美国淋巴瘤嵌合抗原受体 T 细胞治疗联盟的结果。
J Clin Oncol. 2020 Sep 20;38(27):3119-3128. doi: 10.1200/JCO.19.02104. Epub 2020 May 13.
7
Bortezomib with standard chemotherapy for children with acute myeloid leukemia does not improve treatment outcomes: a report from the Children's Oncology Group.硼替佐米联合标准化疗方案治疗儿童急性髓系白血病并未改善治疗结局:来自儿童肿瘤协作组的报告。
Haematologica. 2020 Jul;105(7):1879-1886. doi: 10.3324/haematol.2019.220962. Epub 2020 Feb 6.
8
Mechanisms of resistance to CAR T cell therapies.CAR T 细胞疗法耐药机制。
Semin Cancer Biol. 2020 Oct;65:91-98. doi: 10.1016/j.semcancer.2019.12.002. Epub 2019 Dec 19.
9
Resistance Mechanisms to CAR T-Cell Therapy and Overcoming Strategy in B-Cell Hematologic Malignancies.嵌合抗原受体 T 细胞疗法的耐药机制及在 B 细胞血液恶性肿瘤中的克服策略。
Int J Mol Sci. 2019 Oct 10;20(20):5010. doi: 10.3390/ijms20205010.
10
Exploratory trial of a biepitopic CAR T-targeting B cell maturation antigen in relapsed/refractory multiple myeloma.双表位 CAR T 靶向 B 细胞成熟抗原治疗复发/难治性多发性骨髓瘤的探索性试验。
Proc Natl Acad Sci U S A. 2019 May 7;116(19):9543-9551. doi: 10.1073/pnas.1819745116. Epub 2019 Apr 15.