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霉酚酸酯和来氟米特:治疗皮肤病的有前景的化合物。

Mycophenolate mofetil and leflunomide: promising compounds for the treatment of skin diseases.

作者信息

Frieling U, Luger T A

机构信息

Department of Dermatology, University of Münster, Germany.

出版信息

Clin Exp Dermatol. 2002 Oct;27(7):562-70. doi: 10.1046/j.1365-2230.2002.01150.x.

DOI:10.1046/j.1365-2230.2002.01150.x
PMID:12464151
Abstract

In the past decade, there has been enormous progress in the understanding of the pathomechanisms of immune-mediated diseases, which has led to major advances in immunotherapeutic strategies. As a consequence, the armamentarium of specific and nonspecific immune-modulating and immunosuppressive drugs for the treatment of skin diseases has been widely extended. Among the nonspecific immunomodulators, mycophenolate mofetil and leflunomide show promising effects in a variety of autoimmune and inflammatory skin disorders. Both compounds inhibit a key enzyme in nucleotide biosynthesis, a step that is pivotal for the production of cytotoxic T cells and antibody formation. They do not act in the nucleus, which may explain their advantageous side-effect profile.

摘要

在过去十年中,我们对免疫介导疾病的发病机制的理解取得了巨大进展,这推动了免疫治疗策略的重大进步。因此,用于治疗皮肤病的特异性和非特异性免疫调节及免疫抑制药物的种类得到了广泛扩展。在非特异性免疫调节剂中,霉酚酸酯和来氟米特在多种自身免疫性和炎症性皮肤病中显示出有前景的疗效。这两种化合物都抑制核苷酸生物合成中的一种关键酶,这一步骤对于细胞毒性T细胞的产生和抗体形成至关重要。它们不在细胞核中起作用,这可能解释了它们有利的副作用特征。

相似文献

1
Mycophenolate mofetil and leflunomide: promising compounds for the treatment of skin diseases.霉酚酸酯和来氟米特:治疗皮肤病的有前景的化合物。
Clin Exp Dermatol. 2002 Oct;27(7):562-70. doi: 10.1046/j.1365-2230.2002.01150.x.
2
[Mycophenolate mofetil: a new immunosuppressive drug in dermatology and its possible uses].霉酚酸酯:皮肤科一种新型免疫抑制药物及其可能的用途
Hautarzt. 2000 Feb;51(2):63-9. doi: 10.1007/s001050050013.
3
[Leflunomide--a new drug for pharmacological immunomodulation].
Hautarzt. 2002 May;53(5):309-15. doi: 10.1007/s001050100287.
4
Molecular mechanisms of action of new xenobiotic immunosuppressive drugs: tacrolimus (FK506), sirolimus (rapamycin), mycophenolate mofetil and leflunomide.新型外源性免疫抑制药物的作用分子机制:他克莫司(FK506)、西罗莫司(雷帕霉素)、霉酚酸酯和来氟米特。
Curr Opin Immunol. 1996 Oct;8(5):710-20. doi: 10.1016/s0952-7915(96)80090-2.
5
Triple drug treatment with cyclosporine, leflunomide and mycophenolate mofetil prevents rejection of pig islets transplanted into rats and primates.
Transplant Proc. 1997 Aug;29(5):2498. doi: 10.1016/s0041-1345(97)00463-6.
6
Tacrolimus enhances the immunosuppressive effect of cyclophosphamide but not that of leflunomide or mycophenolate mofetil in a model of discordant liver xenotransplantation.在异种肝移植不匹配模型中,他克莫司增强环磷酰胺的免疫抑制作用,但不增强来氟米特或霉酚酸酯的免疫抑制作用。
Transplant Proc. 1998 Jun;30(4):1091-2. doi: 10.1016/s0041-1345(98)00166-3.
7
Mycophenolic acid in dermatology a century after its discovery.霉酚酸在皮肤病学领域发现百年之后
Australas J Dermatol. 2015 Feb;56(1):77-83. doi: 10.1111/ajd.12259. Epub 2014 Dec 30.
8
Mycophenolate mofetil for the management of autoimmune bullous diseases.霉酚酸酯治疗自身免疫性大疱性疾病。
Dermatol Clin. 2011 Oct;29(4):555-9. doi: 10.1016/j.det.2011.06.012. Epub 2011 Aug 6.
9
Comparison of the therapeutic effects of leflunomide and mycophenolate mofetil in the treatment of immunoglobulin A nephropathy manifesting with nephrotic syndrome.来氟米特与霉酚酸酯治疗表现为肾病综合征的免疫球蛋白A肾病的疗效比较。
Int J Clin Pharmacol Ther. 2010 Aug;48(8):509-13. doi: 10.5414/cpp48509.
10
Diabetic rats transplanted with adult porcine islets and immunosuppressed with cyclosporine, mycophenolate mofetil, and leflunomide remain normoglycemic for up to 100 days.移植了成年猪胰岛并用环孢素、霉酚酸酯和来氟米特进行免疫抑制的糖尿病大鼠可维持长达100天的血糖正常。
Transplant Proc. 2000 Aug;32(5):1061. doi: 10.1016/s0041-1345(00)01119-2.

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The emergence of mycophenolate mofetilin dermatology: from its roots in the world of organ transplantation to its versatile role in the dermatology treatment room.霉酚酸酯在皮肤科的出现:从其在器官移植领域的起源到在皮肤科治疗室的广泛作用。
J Clin Aesthet Dermatol. 2011 Jan;4(1):18-27.
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Emerging treatment of atopic dermatitis.
特应性皮炎的新兴治疗方法。
Clin Rev Allergy Immunol. 2007 Dec;33(3):199-203. doi: 10.1007/s12016-007-0043-6.
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Chronic urticaria: aetiology, management and current and future treatment options.慢性荨麻疹:病因、管理以及当前和未来的治疗选择
Drugs. 2004;64(22):2515-36. doi: 10.2165/00003495-200464220-00003.