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Ecallantide.

作者信息

Zuraw Bruce, Yasothan Uma, Kirkpatrick Peter

出版信息

Nat Rev Drug Discov. 2010 Mar;9(3):189-90. doi: 10.1038/nrd3125.

DOI:10.1038/nrd3125
PMID:20190785
Abstract
摘要

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Ecallantide.艾卡肽德
Nat Rev Drug Discov. 2010 Mar;9(3):189-90. doi: 10.1038/nrd3125.
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Hereditary angioedema--therapies old and new.遗传性血管性水肿——新旧疗法
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3
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Triggers and Prodromal Symptoms of Angioedema Attacks in Patients With Hereditary Angioedema.遗传性血管性水肿患者血管性水肿发作的触发因素和前驱症状
J Investig Allergol Clin Immunol. 2016;26(6):383-386. doi: 10.18176/jiaci.0102.
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Ecallantide for treatment of acute hereditary angioedema attacks: analysis of efficacy by patient characteristics.依卡兰肽治疗急性遗传性血管性水肿发作:按患者特征分析疗效。
Allergy Asthma Proc. 2012 Mar-Apr;33(2):178-85. doi: 10.2500/aap.2012.33.3528.
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Response time for ecallantide treatment of acute hereditary angioedema attacks.依替巴肽治疗急性遗传性血管性水肿发作的反应时间。
Ann Allergy Asthma Immunol. 2010 Dec;105(6):430-436.e2. doi: 10.1016/j.anai.2010.09.005. Epub 2010 Oct 25.
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Ecallantide (DX-88) for acute hereditary angioedema attacks: integrated analysis of 2 double-blind, phase 3 studies.依卡兰肽(DX-88)治疗急性遗传性血管性水肿发作:两项双盲、3 期研究的汇总分析。
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Icatibant.依卡替班
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Current and emerging therapies to prevent hereditary angioedema attacks.目前和新兴的预防遗传性血管性水肿发作的疗法。
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New treatments addressing the pathophysiology of hereditary angioedema.针对遗传性血管性水肿病理生理学的新疗法。
Clin Mol Allergy. 2008 Apr 14;6:2. doi: 10.1186/1476-7961-6-2.
2
Critical role of kallikrein in hereditary angioedema pathogenesis: a clinical trial of ecallantide, a novel kallikrein inhibitor.激肽释放酶在遗传性血管性水肿发病机制中的关键作用:新型激肽释放酶抑制剂依库珠单抗的一项临床试验
J Allergy Clin Immunol. 2007 Aug;120(2):416-22. doi: 10.1016/j.jaci.2007.04.028. Epub 2007 Jun 7.
3
Plasma bradykinin in angio-oedema.血管性水肿中的血浆缓激肽。
SYNBIP:用于研究、诊断和治疗的合成结合蛋白。
Nucleic Acids Res. 2022 Jan 7;50(D1):D560-D570. doi: 10.1093/nar/gkab926.
4
Icatibant promotes patients' behavior modification associated with emergency room visits during an acute attack of hereditary angioedema.依卡替班可促进遗传性血管性水肿急性发作期间与急诊就诊相关的患者行为改变。
Intractable Rare Dis Res. 2021 May;10(2):142-145. doi: 10.5582/irdr.2021.01010.
5
Molecular Mechanisms of Premature Aging in Hemodialysis: The Complex Interplay Between Innate and Adaptive Immune Dysfunction.血液透析患者过早衰老的分子机制:固有和适应性免疫功能障碍的复杂相互作用。
Int J Mol Sci. 2020 May 12;21(10):3422. doi: 10.3390/ijms21103422.
6
Novel MASP-2 inhibitors developed via directed evolution of human TFPI1 are potent lectin pathway inhibitors.通过定向进化人 TFPI1 开发的新型 MASP-2 抑制剂是有效的凝集素途径抑制剂。
J Biol Chem. 2019 May 17;294(20):8227-8237. doi: 10.1074/jbc.RA119.008315. Epub 2019 Apr 5.
7
Phage display-derived human antibodies in clinical development and therapy.临床开发与治疗中基于噬菌体展示技术获得的人源抗体。
MAbs. 2016 Oct;8(7):1177-1194. doi: 10.1080/19420862.2016.1212149. Epub 2016 Jul 14.
8
Extremophilic 50S Ribosomal RNA-Binding Protein L35Ae as a Basis for Engineering of an Alternative Protein Scaffold.嗜极端环境的50S核糖体RNA结合蛋白L35Ae作为构建替代蛋白质支架的基础
PLoS One. 2015 Aug 6;10(8):e0134906. doi: 10.1371/journal.pone.0134906. eCollection 2015.
9
Management of acute attacks of hereditary angioedema: role of ecallantide.遗传性血管性水肿急性发作的管理:依库珠单抗的作用
J Blood Med. 2015 Apr 16;6:115-23. doi: 10.2147/JBM.S66825. eCollection 2015.
10
Unleashing the therapeutic potential of human kallikrein-related serine proteases.释放人激肽释放酶相关丝氨酸蛋白酶的治疗潜力。
Nat Rev Drug Discov. 2015 Mar;14(3):183-202. doi: 10.1038/nrd4534. Epub 2015 Feb 20.
Lancet. 1998 Jun 6;351(9117):1693-7. doi: 10.1016/S0140-6736(97)09137-X.
4
Obtaining a family of high-affinity, high-specificity protein inhibitors of plasmin and plasma kallikrein.获得一组纤溶酶和血浆激肽释放酶的高亲和力、高特异性蛋白抑制剂。
Mol Divers. 1996 Oct;2(1-2):119-24. doi: 10.1007/BF01718709.
5
Iterative optimization of high-affinity protease inhibitors using phage display. 2. Plasma kallikrein and thrombin.利用噬菌体展示技术对高亲和力蛋白酶抑制剂进行迭代优化。2. 血浆激肽释放酶和凝血酶。
Biochemistry. 1996 Jun 18;35(24):8058-67. doi: 10.1021/bi952629y.