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优化地尼白介素妥西罗汀(昂他克)疗法。

Optimizing denileukin diftitox (Ontak) therapy.

作者信息

Duvic Madeleine, Talpur Rakhshandra

机构信息

The University of Texas MD Anderson Cancer Center, Division of Internal Medicine, Department of Dermatology, 1515 Holcombe Blvd, Unit 1452, Houston, TX 77030, USA.

出版信息

Future Oncol. 2008 Aug;4(4):457-69. doi: 10.2217/14796694.4.4.457.

Abstract

Denileukin diftitox (Ontak) is a novel recombinant fusion protein consisting of peptide sequences for the enzymatically active and membrane translocation domain of diphtheria toxin linked to human IL-2. Denileukin diftitox specifically binds to IL-2 receptors on the cell membrane, is internalized via receptor-mediated endocytosis and inhibits protein synthesis by ADP ribosylation of elongation factor 2, resulting in cell death. This article focuses on the clinical trial that led to the US FDA approval of the drug for cutaneous T-cell lymphoma in 1999, and other investigational studies for hematologic malignancies, recurrent and refractory chronic lymphocytic leukemia, non-Hodgkin B-cell lymphoma, graft-versus-host disease and autoimmune disease, demonstrating the activity and adverse effects of the drug.

摘要

地尼白介素-匹伏毒素(Ontak)是一种新型重组融合蛋白,由与人类白细胞介素-2相连的白喉毒素酶活性和膜转位结构域的肽序列组成。地尼白介素-匹伏毒素特异性结合细胞膜上的白细胞介素-2受体,通过受体介导的内吞作用被内化,并通过对延伸因子2进行ADP核糖基化来抑制蛋白质合成,从而导致细胞死亡。本文重点介绍了1999年导致美国食品药品监督管理局(FDA)批准该药物用于皮肤T细胞淋巴瘤的临床试验,以及针对血液系统恶性肿瘤、复发和难治性慢性淋巴细胞白血病、非霍奇金B细胞淋巴瘤、移植物抗宿主病和自身免疫性疾病的其他研究,展示了该药物的活性和不良反应。

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