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用于自身免疫性关节炎的耐受性DNA疫苗。

Tolerizing DNA vaccines for autoimmune arthritis.

作者信息

Ho Peggy P, Higgins John P, Kidd Brian A, Tomooka Beren, Digennaro Carla, Lee Lowen Y, de Vegvar Henry E Neuman, Steinman Lawrence, Robinson William H

机构信息

Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA 94305, USA.

出版信息

Autoimmunity. 2006 Dec;39(8):675-82. doi: 10.1080/08916930601061603.

Abstract

Current therapies for rheumatoid arthritis (RA) and other autoimmune diseases non-specifically suppress immune function, and there is great need for fundamental approaches such as antigen-specific tolerizing therapy. In this paper we describe development of antigen-specific tolerizing DNA vaccines to treat collagen-induced arthritis (CIA) in mice, and use of protein microarrays to monitor response to therapy and to identify potential additional autoimmune targets for next generation vaccines. We demonstrate that tolerizing DNA vaccines encoding type II collagen (CII) reduced the incidence and severity of CIA. Atorvastatin, a statin drug found to reduce the severity of autoimmunity, potentiated the effect of DNA vaccines encoding CII. Analysis of cytokines produced by collagen-reactive T cells derived from mice receiving tolerizing DNA encoding CII, as compared to control vaccines, revealed reduced production of the pro-inflammatory cytokines IFN-gamma and TNF-alpha. Arthritis microarray analysis demonstrated reduced spreading of autoantibody responses in mice treated with DNA encoding CII. The development of tolerizing DNA vaccines, and the use of antibody profiling to guide design of and to monitor therapeutic responses to such vaccines, represents a promising approach for the treatment of RA and other autoimmune diseases.

摘要

目前用于治疗类风湿性关节炎(RA)和其他自身免疫性疾病的疗法会非特异性地抑制免疫功能,因此对抗原特异性耐受疗法等根本性方法有很大需求。在本文中,我们描述了用于治疗小鼠胶原诱导性关节炎(CIA)的抗原特异性耐受DNA疫苗的研发,以及使用蛋白质微阵列来监测对治疗的反应并确定下一代疫苗潜在的其他自身免疫靶点。我们证明,编码II型胶原(CII)的耐受DNA疫苗降低了CIA的发病率和严重程度。阿托伐他汀是一种被发现可减轻自身免疫严重程度的他汀类药物,它增强了编码CII的DNA疫苗的效果。与对照疫苗相比,对接受编码CII的耐受DNA的小鼠来源的胶原反应性T细胞产生的细胞因子进行分析,发现促炎细胞因子IFN-γ和TNF-α的产生减少。关节炎微阵列分析表明,在用编码CII的DNA治疗的小鼠中自身抗体反应的扩散减少。耐受DNA疫苗的研发以及使用抗体谱分析来指导此类疫苗的设计和监测治疗反应,代表了一种治疗RA和其他自身免疫性疾病的有前景的方法。

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