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[系统性红斑狼疮治疗的新概念]

[New concepts for the therapy of systemic lupus erythematosus].

作者信息

Spertini François

机构信息

Service d'immunologie et d'allergie, CHUV, Lausanne.

出版信息

Rev Med Suisse. 2007 Jan 17;3(94):98-102.

Abstract

Immediate, short- and long-term adverse events of classical immunosuppressor drugs strongly stimulate novel, but less toxic approaches. Combined or sequential use of cyclophosphamide, mycophénolate mofétil and/ or azathioprine should improve clinical tolerance and avoid severe adverse events (infections, infertility, amenorrhea), regularly associated to long term therapies with classical immunosuppressive schemes. Among novel developments based on biologicals, the anti-CD20 monoclonal antibody rituximab (anti-B cells) appears encouraging in open studies, in association or not with cyclophosphamide, and is generally well tolerated. Further information is expected from the inhibitor of T cell/B cell co-stimulation CTLA4-Ig, or from strategies aiming to inhibit key cytokines in SLE pathogenesis such as interferon-alpha, IL-1 or IL-6.

摘要

传统免疫抑制剂药物的即刻、短期和长期不良事件有力地推动了新型但毒性较小的治疗方法的发展。联合或序贯使用环磷酰胺、霉酚酸酯和/或硫唑嘌呤应可提高临床耐受性,并避免严重不良事件(感染、不孕、闭经),这些不良事件通常与传统免疫抑制方案的长期治疗相关。在基于生物制剂的新进展中,抗CD20单克隆抗体利妥昔单抗(抗B细胞)在开放研究中,无论是否与环磷酰胺联合使用,似乎都令人鼓舞,且总体耐受性良好。预计来自T细胞/B细胞共刺激抑制剂CTLA4-Ig或旨在抑制系统性红斑狼疮发病机制中的关键细胞因子(如α干扰素、白细胞介素-1或白细胞介素-6)的策略将提供更多信息。

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