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TNF 家族成员 APRIL 抑制胶原诱导性关节炎。

The TNF family member APRIL dampens collagen-induced arthritis.

机构信息

Institut de Génétique Moléculaire de Montpellier, CNRS, Montpellier, France.

出版信息

Ann Rheum Dis. 2013 Aug;72(8):1367-74. doi: 10.1136/annrheumdis-2012-202382. Epub 2012 Nov 24.

Abstract

BACKGROUND

The tumour necrosis factor (TNF)-family members B cell activating factor (BAFF) and A PRoliferation-Inducing Ligand (APRIL) play important roles in B cell biology, and share binding to B cell maturation antigen and transmembrane activator and cyclophilin ligand interactor, both receptors of the TNF-family. However, while it is reported that BAFF can break B cell tolerance, the role of APRIL in autoimmunity remains elusive.

OBJECTIVE

To evaluate the role of APRIL on collagen-induced arthritis (CIA).

METHODS

CIA was induced in APRIL-transgenic (Tg) DBA/1 mice and littermates. Disease progression was evaluated by clinical and histological signs of arthritis. In another experimental setting mice were exposed to the collagen antibody-induced arthritis. In addition, we tested T cell dependent humoral responses in APRIL-Tg mice.

RESULTS

We found that APRIL-Tg displayed a strongly reduced incidence and severity of CIA compared with littermates, with decreases in collagen-specific autoantibody titres, immune complex deposition and downstream mast cell activation in joints. Notably, ectopic APRIL-expression was also found to negatively regulate T cell dependent humoral responses. The lower autoantibody production in APRIL-Tg mice during CIA appears to be crucial, as arthritis induced by administration of anti-collagen antibodies developed similar in APRIL-Tg and control mice, thus demonstrating that the downstream effector pathways induced by anti-collagen antibodies remain intact in APRIL-Tg mice. This protective effect was specifically mediated by APRIL, as adenoviral delivery of APRIL decreased CIA in a therapeutic setting.

CONCLUSIONS

Collectively, our data identify APRIL as a negative regulator of CIA by regulating autoantibody production. These findings are of important clinical relevance, as the therapeutic potential of transmembrane activator and cyclophilin ligand interactor-Fc (atacicept) is presently evaluated in clinical trials.

摘要

背景

肿瘤坏死因子(TNF)家族成员 B 细胞激活因子(BAFF)和 A 增殖诱导配体(APRIL)在 B 细胞生物学中发挥重要作用,并且都与 B 细胞成熟抗原和跨膜激活剂和环孢素配体相互作用(TACI)结合,TACI 是 TNF 家族的受体。然而,虽然据报道 BAFF 可以打破 B 细胞耐受,但 APRIL 在自身免疫中的作用仍不清楚。

目的

评估 APRIL 在胶原诱导关节炎(CIA)中的作用。

方法

在 APRIL 转基因(Tg)DBA/1 小鼠及其同窝仔鼠中诱导 CIA。通过关节炎的临床和组织学迹象评估疾病进展。在另一个实验环境中,用胶原抗体诱导关节炎来检测小鼠。此外,我们还在 APRIL-Tg 小鼠中测试了 T 细胞依赖的体液反应。

结果

我们发现,与同窝仔鼠相比,APRIL-Tg 显示 CIA 的发病率和严重程度明显降低,胶原特异性自身抗体滴度、免疫复合物沉积和关节中下游肥大细胞激活减少。值得注意的是,异位 APRIL 表达也被发现可负调控 T 细胞依赖的体液反应。在 CIA 期间,APRIL-Tg 小鼠产生的自身抗体减少似乎至关重要,因为抗胶原抗体诱导的关节炎在 APRIL-Tg 和对照小鼠中发展相似,从而表明抗胶原抗体诱导的下游效应途径在 APRIL-Tg 小鼠中仍然完整。这种保护作用是由 APRIL 特异性介导的,因为在治疗性环境中,腺病毒递送 APRIL 可降低 CIA 的发病。

结论

总的来说,我们的数据将 APRIL 确定为 CIA 的负调节剂,通过调节自身抗体的产生来发挥作用。这些发现具有重要的临床意义,因为跨膜激活剂和环孢素配体相互作用(TACI)-Fc 的治疗潜力目前正在临床试验中进行评估。

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