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系统性红斑狼疮的新疗法。

Novel treatments for systemic lupus erythematosus.

机构信息

Newark Beth Israel Medical Center - Rheumatology, Newark, New Jersey, USA.

出版信息

Ther Adv Musculoskelet Dis. 2011 Oct;3(5):255-66. doi: 10.1177/1759720X11415456.

Abstract

There are many new therapeutic directions for the disease systemic lupus erythematosus (SLE). Despite this, the US Food and Drug Administration (FDA) has approved only one biological agent and it involves B cells, now thought to play a significant role in the pathogenesis of SLE. The name of the drug is belimumab, which is an agent that removes the B-cell cytokine called B lymphocyte stimulation factor (BLyS). Rituximab did not achieve its primary endpoints, even though the consensus is that it may be effective in some forms of SLE including renal disease. The anticytokine therapies against interleukin (IL)-6, IL-10, IL-17 and tumor necrosis factor (TNF) are effective in their own ways and phase II and III trials are in progress. Of particular interest to immunologists are the anti-interferon alpha and gamma drugs, which show promise in the animal models. Modulation of costimulatory molecules; specifically, the anti CD40, CTLA-***Ig and ICOS/B7RP blockade agents offer possibilities for the future using new pathways heretofore limited to rheumatoid arthritis. Finally, the use of tyrosine kinase inhibitors is another direction that has been successful in the inhibition of SLE in the murine model; early trials in human SLE have begun.

摘要

针对系统性红斑狼疮 (SLE) 疾病,存在许多新的治疗方向。尽管如此,美国食品和药物管理局 (FDA) 仅批准了一种生物制剂,该制剂涉及 B 细胞,现在认为 B 细胞在 SLE 的发病机制中起重要作用。该药物的名称为贝利木单抗,这是一种可去除 B 细胞细胞因子(B 淋巴细胞刺激因子,BLyS)的药物。尽管人们普遍认为利妥昔单抗可能对某些类型的 SLE(包括肾脏疾病)有效,但它甚至没有达到其主要终点。针对白细胞介素 (IL)-6、IL-10、IL-17 和肿瘤坏死因子 (TNF) 的抗细胞因子疗法在各自的治疗领域中均具有疗效,并且正在进行 II 期和 III 期临床试验。特别令免疫学家感兴趣的是针对干扰素-α和γ的药物,这些药物在动物模型中显示出了一定的疗效。共刺激分子的调节;特别是抗 CD40、CTLA-***Ig 和 ICOS/B7RP 阻断剂,为未来提供了可能性,这些可能性为以前仅限于类风湿关节炎的途径提供了可能。最后,酪氨酸激酶抑制剂的使用是另一个在抑制 SLE 方面在鼠模型中已取得成功的方向;已开始在人类 SLE 中进行早期试验。

相似文献

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Novel treatments for systemic lupus erythematosus.系统性红斑狼疮的新疗法。
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