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Targeting CD300f to enhance hematopoietic stem cell transplantation in acute myeloid leukemia.靶向CD300f以增强急性髓系白血病中的造血干细胞移植。
Blood Adv. 2020 Apr 14;4(7):1206-1216. doi: 10.1182/bloodadvances.2019001289.
2
Safety and efficacy of talacotuzumab plus decitabine or decitabine alone in patients with acute myeloid leukemia not eligible for chemotherapy: results from a multicenter, randomized, phase 2/3 study.塔拉唑单抗联合地西他滨或地西他滨单独治疗不适合化疗的急性髓系白血病患者的安全性和有效性:来自多中心、随机、2/3 期研究的结果。
Leukemia. 2021 Jan;35(1):62-74. doi: 10.1038/s41375-020-0773-5. Epub 2020 Mar 16.
3
Is Hematopoietic Stem Cell Transplantation Required to Unleash the Full Potential of Immunotherapy in Acute Myeloid Leukemia?急性髓系白血病中释放免疫疗法的全部潜力是否需要造血干细胞移植?
J Clin Med. 2020 Feb 18;9(2):554. doi: 10.3390/jcm9020554.
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Therapeutic Targeting of the Macrophage Immune Checkpoint CD47 in Myeloid Malignancies.髓系恶性肿瘤中巨噬细胞免疫检查点CD47的治疗靶向作用
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Nat Rev Cancer. 2020 Mar;20(3):158-173. doi: 10.1038/s41568-019-0230-9. Epub 2020 Jan 6.
6
Immunotherapy-Based Targeting and Elimination of Leukemic Stem Cells in AML and CML.基于免疫疗法的 AML 和 CML 中白血病干细胞的靶向和清除。
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Immunotherapy with HDC/IL-2 may be clinically efficacious in acute myeloid leukemia of normal karyotype.高剂量化疗/白细胞介素 2 免疫疗法可能对正常核型急性髓系白血病具有临床疗效。
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Blood Rev. 2019 Sep;37:100578. doi: 10.1016/j.blre.2019.05.002. Epub 2019 May 11.
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A Chemo-enzymatically Linked Bispecific Antibody Retargets T Cells to a Sialylated Epitope on CD43 in Acute Myeloid Leukemia.一种化学酶连接的双特异性抗体将 T 细胞重新靶向到急性髓系白血病中 CD43 上的唾液酸化表位。
Cancer Res. 2019 Jul 1;79(13):3372-3382. doi: 10.1158/0008-5472.CAN-18-0189. Epub 2019 May 7.
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Tagraxofusp in Blastic Plasmacytoid Dendritic-Cell Neoplasm.塔拉唑滨治疗原始浆细胞样树突状细胞瘤。
N Engl J Med. 2019 Apr 25;380(17):1628-1637. doi: 10.1056/NEJMoa1815105.

针对急性髓系白血病中白血病干细胞的基于细胞和抗体的免疫疗法:观点和未解决的问题。

Cell-based and antibody-mediated immunotherapies directed against leukemic stem cells in acute myeloid leukemia: Perspectives and open issues.

机构信息

Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.

Ludwig Boltzmann Institute for Hematology & Oncology, Medical University of Vienna, Vienna, Austria.

出版信息

Stem Cells Transl Med. 2020 Nov;9(11):1331-1343. doi: 10.1002/sctm.20-0147. Epub 2020 Jul 13.

DOI:10.1002/sctm.20-0147
PMID:32657052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7581453/
Abstract

Despite new insights in molecular features of leukemic cells and the availability of novel treatment approaches and drugs, acute myeloid leukemia (AML) remains a major clinical challenge. In fact, many patients with AML relapse after standard therapy and eventually die from progressive disease. The basic concept of leukemic stem cells (LSC) has been coined with the goal to decipher clonal architectures in various leukemia-models and to develop curative drug therapies by eliminating LSC. Indeed, during the past few years, various immunotherapies have been tested in AML, and several of these therapies follow the strategy to eliminate relevant leukemic subclones by introducing LSC-targeting antibodies or LSC-targeting immune cells. These therapies include, among others, new generations of LSC-eliminating antibody-constructs, checkpoint-targeting antibodies, bi-specific antibodies, and CAR-T or CAR-NK cell-based strategies. However, responses are often limited and/or transient which may be due to LSC resistance. Indeed, AML LSC exhibit multiple forms of resistance against various drugs and immunotherapies. An additional problems are treatment-induced myelotoxicity and other side effects. The current article provides a short overview of immunological targets expressed on LSC in AML. Moreover, cell-based therapies and immunotherapies tested in AML are discussed. Finally, the article provides an overview about LSC resistance and strategies to overcome resistance.

摘要

尽管在白血病细胞的分子特征方面有了新的认识,并且有了新的治疗方法和药物,但急性髓细胞白血病(AML)仍然是一个主要的临床挑战。事实上,许多 AML 患者在标准治疗后复发,最终死于疾病进展。白血病干细胞(LSC)的基本概念是为了解释各种白血病模型中的克隆结构,并通过消除 LSC 来开发治愈性药物治疗。事实上,在过去的几年中,已经在 AML 中测试了各种免疫疗法,其中一些疗法通过引入针对 LSC 的抗体或针对 LSC 的免疫细胞来消除相关的白血病亚克隆,从而遵循消除 LSC 的策略。这些疗法包括新一代的 LSC 消除抗体构建物、检查点靶向抗体、双特异性抗体以及基于 CAR-T 或 CAR-NK 细胞的策略。然而,反应往往是有限的和/或短暂的,这可能是由于 LSC 耐药性所致。事实上,AML LSC 对各种药物和免疫疗法表现出多种形式的耐药性。另一个问题是治疗引起的骨髓毒性和其他副作用。本文简要概述了 AML 中 LSC 上表达的免疫靶标。此外,还讨论了在 AML 中测试的基于细胞的疗法和免疫疗法。最后,本文概述了 LSC 耐药性以及克服耐药性的策略。