Mozobil® (Plerixafor, AMD3100), 10 years after its approval by the US Food and Drug Administration.

Q2 Pharmacology, Toxicology and Pharmaceutics Antiviral Chemistry and Chemotherapy Pub Date : 2019-01-01 DOI:10.1177/2040206619829382
Erik De Clercq
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引用次数: 86

Abstract

AMD3100 (plerixafor, Mozobil®) was first identified as an anti-HIV agent specifically active against the T4-lymphotropic HIV strains, as it selectively blocked the CXCR4 receptor. Through interference with the interaction of CXCR4 with its natural ligand, SDF-1 (also named CXCL12), it also mobilized the CD34+stem cells from the bone marrow into the peripheral blood stream. In December 2008, AMD3100 was formally approved by the US FDA for autologous transplantation in patients with Non-Hodgkin's Lymphoma or multiple myeloma. It may be beneficially used in various other malignant diseases as well as hereditary immunological disorders such as WHIM syndrome, and physiopathological processes such as hepatopulmonary syndrome.

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Mozobil®(Plerixafor, AMD3100),获得美国食品和药物管理局批准10年后。
AMD3100 (plerixafor, Mozobil®)最初被确定为一种抗HIV药物,可选择性阻断CXCR4受体,对t4淋巴细胞性HIV毒株具有特异性活性。通过干扰CXCR4与其天然配体SDF-1(也称为CXCL12)的相互作用,它还将骨髓中的CD34+干细胞动员到外周血中。2008年12月,AMD3100被美国FDA正式批准用于非霍奇金淋巴瘤或多发性骨髓瘤患者的自体移植。它可以有益地用于各种其他恶性疾病以及遗传性免疫疾病,如WHIM综合征,以及肝肺综合征等生理病理过程。
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来源期刊
Antiviral Chemistry and Chemotherapy
Antiviral Chemistry and Chemotherapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.20
自引率
0.00%
发文量
5
审稿时长
15 weeks
期刊介绍: Antiviral Chemistry & Chemotherapy publishes the results of original research concerned with the biochemistry, mode of action, chemistry, pharmacology and virology of antiviral compounds. Manuscripts dealing with molecular biology, animal models and vaccines are welcome. The journal also publishes reviews, pointers, short communications and correspondence.
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