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血液系统恶性肿瘤的免疫毒素疗法。

Immunotoxin therapy of hematologic malignancies.

作者信息

Frankel Arthur E, Neville David M, Bugge Thomas A, Kreitman Robert J, Leppla Stephen H

机构信息

Wake Forest University School of Medicine, Winston-Salem, NC, USA.

出版信息

Semin Oncol. 2003 Aug;30(4):545-57. doi: 10.1016/s0093-7754(03)00241-0.

Abstract

Patients with chemotherapy relapsed or refractory hematologic malignancies may be effectively treated with allogeneic or autologous stem cell transplants. However, many patients cannot be transplanted due to age, comorbidities, or lack of suitable donors. Further, a fraction of patients relapse post-transplant. Novel therapeutic agents that can kill multidrug-resistant malignant stem cells and are not myelosuppressive are needed. One class of such agents is immunotoxins. Immunotoxins consist of cell-selective ligands covalently linked to peptide toxins. The ligand delivers the molecule to specific cell surface receptors on malignant cells. The toxin triggers cell death either by reaching the cytosol and catalytically inactivating vital cell processes or by modifying the tumor cell surface membrane. We have synthesized immunotoxins for therapy of chemoresistant hematologic diseases. In this review, we will detail the synthesis of a number of these drugs and describe their preclinical and clinical activity. Several of these agents have shown dramatic antitumor effects in patients with hematologic neoplasms, and one immunotoxin has been approved for use by the US Food and Drug Administration (FDA). Over the next several decades, a growing number of these agents should reach the clinic.

摘要

化疗复发或难治性血液系统恶性肿瘤患者可通过异基因或自体干细胞移植得到有效治疗。然而,许多患者由于年龄、合并症或缺乏合适的供体而无法进行移植。此外,一部分患者在移植后会复发。因此,需要能够杀死多药耐药恶性干细胞且无骨髓抑制作用的新型治疗药物。免疫毒素就是这类药物中的一种。免疫毒素由与肽毒素共价连接的细胞选择性配体组成。配体将分子递送至恶性细胞上的特定细胞表面受体。毒素通过进入细胞质并催化使重要细胞过程失活,或通过修饰肿瘤细胞表面膜来触发细胞死亡。我们已经合成了用于治疗化疗耐药血液系统疾病的免疫毒素。在这篇综述中,我们将详细介绍其中几种药物的合成,并描述它们的临床前和临床活性。其中几种药物已在血液系统肿瘤患者中显示出显著的抗肿瘤作用,并且一种免疫毒素已被美国食品药品监督管理局(FDA)批准使用。在未来几十年里,这类药物中将会有越来越多进入临床应用。

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