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利妥昔单抗(抗CD20)治疗累及中枢神经系统的难治性系统性红斑狼疮的疗效

Efficacy of rituximab (anti-CD20) for refractory systemic lupus erythematosus involving the central nervous system.

作者信息

Tokunaga Mikiko, Saito Kazuyoshi, Kawabata Daisuke, Imura Yoshitaka, Fujii Takao, Nakayamada Shingo, Tsujimura Shizuyo, Nawata Masao, Iwata Shigeru, Azuma Taeko, Mimori Tsuneyo, Tanaka Yoshiya

机构信息

The First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Japan, 1-1 Iseigaoka Yahata-nishi, Kitakyushu 807-8555 Japan.

出版信息

Ann Rheum Dis. 2007 Apr;66(4):470-5. doi: 10.1136/ard.2006.057885. Epub 2006 Nov 15.

Abstract

AIM

Neuropsychiatric systemic lupus erythematosus (NPSLE) is a serious treatment-resistant phenotype of systemic lupus erythematosus. A standard treatment for NPSLE is not available. This report describes the clinical and laboratory tests of 10 patients with NPSLE before and after rituximab treatment, including changes in lymphocyte phenotypes.

METHODS

Rituximab was administered at different doses in 10 patients with refractory NPSLE, despite intensive treatment.

RESULTS

Treatment with rituximab resulted in rapid improvement of central nervous system-related manifestations, particularly acute confusional state. Rituximab also improved cognitive dysfunction, psychosis and seizure, and reduced the SLE Disease Activity Index Score at day 28 in all 10 patients. These effects lasted for >1 year in five patients. Flow cytometric analysis showed that rituximab down regulated CD40 and CD80 on B cells and CD40L, CD69 and inducible costimulator on CD4+ T cells.

CONCLUSIONS

Rituximab rapidly improved refractory NPSLE, as evident by resolution of various clinical signs and symptoms and improvement of radiographic findings. The down regulation of functional molecules on B and T cells suggests that rituximab modulates the interaction of activated B and T cells through costimulatory molecules. These results warrant further analysis of rituximab as treatment for NPSLE.

摘要

目的

神经精神性系统性红斑狼疮(NPSLE)是系统性红斑狼疮一种严重且难治的表型。目前尚无针对NPSLE的标准治疗方法。本报告描述了10例NPSLE患者在接受利妥昔单抗治疗前后的临床及实验室检查情况,包括淋巴细胞表型的变化。

方法

尽管进行了强化治疗,但仍对10例难治性NPSLE患者给予不同剂量的利妥昔单抗治疗。

结果

利妥昔单抗治疗使中枢神经系统相关表现迅速改善,尤其是急性意识模糊状态。利妥昔单抗还改善了认知功能障碍、精神病和癫痫发作,并在第28天时降低了所有10例患者的系统性红斑狼疮疾病活动指数评分。其中5例患者的这些效果持续超过1年。流式细胞术分析显示,利妥昔单抗下调了B细胞上的CD40和CD80以及CD4⁺T细胞上的CD40L、CD69和诱导性共刺激分子。

结论

利妥昔单抗迅速改善了难治性NPSLE,各种临床体征和症状的缓解以及影像学表现的改善均证明了这一点。B细胞和T细胞上功能分子的下调表明,利妥昔单抗通过共刺激分子调节活化的B细胞和T细胞之间的相互作用。这些结果值得对利妥昔单抗作为NPSLE的治疗方法进行进一步分析。

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