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[用新型免疫抑制剂克拉屈滨(2-氯脱氧腺苷)治疗多发性硬化症。理论基础与初步结果]

[Treatment of multiple sclerosis with cladribine (2-CDA), a new immunosuppressant agent. Theoretical basis and preliminary results].

作者信息

Grieb P, Stelmasiak Z

机构信息

Instytutu-Centrum Medycyny Doświadczalnej i Klinicznej PAN w Warszawie.

出版信息

Neurol Neurochir Pol. 1995 Jan-Feb;29(1):69-76.

PMID:7596480
Abstract

The rationale for immunosuppressive treatment of multiple sclerosis comes from current concepts of pathogenesis of this disease. However, clinical effects of immunosuppression have been largely disappointing. Cladribine (chloro-2'-deoxyadenosine, 2CdA) is a new antileukaemic drug which also shows a strong immunosuppressive activity in vitro and in vivo. Being successfully used to treat lymphoproliferative diseases during last few years, cladribine is currently tested in multiple sclerosis. Preliminary results of two independent randomized, placebo-controlled trials are very promising. The indicate that treatment with cladribine may halt the progression of chronic progressive MS, and decrease the frequency of relapses and improve neurological status in remitting-relapsing stage of the disease.

摘要

对多发性硬化症进行免疫抑制治疗的理论依据源于对该疾病发病机制的当前认识。然而,免疫抑制的临床效果在很大程度上令人失望。克拉屈滨(氯-2'-脱氧腺苷,2CdA)是一种新型抗白血病药物,在体外和体内均表现出强大的免疫抑制活性。在过去几年中成功用于治疗淋巴增殖性疾病后,克拉屈滨目前正在多发性硬化症中进行试验。两项独立的随机、安慰剂对照试验的初步结果非常有前景。这些结果表明,克拉屈滨治疗可能会阻止慢性进展性多发性硬化症的进展,并降低复发频率,改善疾病缓解-复发阶段的神经状态。

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