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克罗恩病中的免疫抑制药物。

Immunosuppressive drugs in Crohn's disease.

作者信息

Kornbluth A, George J, Sachar D B

机构信息

Mount Sinai School of Medicine, City University, New York, NY.

出版信息

Gastroenterologist. 1994 Sep;2(3):239-46.

PMID:7987622
Abstract

We review clinical experience with the immunosuppressive drugs 6-mercaptopurine (6-MP) and azathioprine, cyclosporine, and methotrexate in the management of patients with Crohn's disease. 6-MP and azathioprine are closely related structurally. Their exact mechanism of action is unknown, but both cause immunosuppression by interfering with nucleic acid metabolism in the immunological sequence that follows antigenic stimulation. 6-MP and azathioprine have proved most useful for two indications: reducing steroid requirements and healing fistulas. Among patients who are dependent on steroids for control of active inflammatory Crohn's disease, approximately 50% can be completely weaned from prednisone, and an additional 25% can tolerate a substantial dose reduction when treated with 6-MP or azathioprine. Likewise, 6-MP is effective in closing fistulas in approximately one third of patients and in reducing fistula drainage in an additional one third. However, the onset of action is slow and the results may be dose dependent. Cyclosporine, a selective immunosuppressant drug, inhibits T lymphocytes by inhibiting expression of interleukin-2 and its receptors. Its principal usefulness may be in patients with disabling fistulas or active steroid-refractory colitis who cannot tolerate the several months required for a remission induced by 6-MP or azathioprine. Methotrexate, a dihydrofolate reductase inhibitor, has antimetabolite and antiinflammatory properties. Methotrexate is only slightly, if at all, faster acting than 6-MP or azathioprine. Its principal usefulness may therefore be in cases when these other drugs have not been tolerated or are ineffective.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们回顾了免疫抑制药物6-巯基嘌呤(6-MP)、硫唑嘌呤、环孢素和甲氨蝶呤在治疗克罗恩病患者中的临床经验。6-MP和硫唑嘌呤在结构上密切相关。它们的确切作用机制尚不清楚,但两者均通过干扰抗原刺激后免疫反应序列中的核酸代谢来引起免疫抑制。6-MP和硫唑嘌呤已被证明对两种情况最为有用:减少类固醇需求和治愈瘘管。在依赖类固醇来控制活动性炎症性克罗恩病的患者中,约50%可以完全停用泼尼松,另外25%在接受6-MP或硫唑嘌呤治疗时能够耐受大幅剂量减少。同样,6-MP在约三分之一的患者中可有效闭合瘘管,另外三分之一的患者瘘管引流减少。然而,起效缓慢,结果可能与剂量有关。环孢素是一种选择性免疫抑制药物,通过抑制白细胞介素-2及其受体的表达来抑制T淋巴细胞。其主要用途可能在于患有致残性瘘管或活动性类固醇难治性结肠炎且无法耐受6-MP或硫唑嘌呤诱导缓解所需数月时间的患者。甲氨蝶呤是一种二氢叶酸还原酶抑制剂,具有抗代谢和抗炎特性。甲氨蝶呤的起效速度即便比6-MP或硫唑嘌呤快,也只是略快一点。因此,其主要用途可能在于其他药物无法耐受或无效的情况。(摘要截选至250词)

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