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Letters to the editor-Giant cell arteritis-can wwe decrease its relapsing course with less toxic therapy?

机译:给编辑的信-巨细胞性动脉炎-我们可以通过减少毒性的治疗来减少其复发过程吗?

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We read with great interest the excellent review article "Giant cell arteritis-a changing entity" by Kesten et al. [1], As the authors note, glucocorticoids are still the mainstay of therapy in patients with giant cell arteritis (CGA). However, relapses often occur during cortico-steroid tapering and adverse effects are frequent, especially in the elderly population. At present, methotrexate is used as a corticosteroid-sparing drug, which is not devoid of toxicity. Thus, an effective and safe corticosteroid-sparing drug would be desirable. As Kesten and colleagues [1] mention, at least two distinct CD4+ T-cell subsets, namely Thl 7 and Thl cells, promote vascular inflammation in GCA. Thl 7 cells are explicitly corticosteroid-sensitive. However, Thl cells are corticosteroid-resistant and abnormal Thl responses continue, unaffected by corticosteroids, identifying GCA as a long-term, chronic immune-mediated disease. Interferon-gamma is the signature cytokine produced by the Thl cell lineage.
机译:我们非常感兴趣地阅读了Kesten等人的优秀评论文章“巨细胞动脉炎-不断变化的实体”。 [1],正如作者所指出的那样,糖皮质激素仍然是巨细胞动脉炎(CGA)患者的主要治疗手段。但是,在皮质类固醇逐渐减少期间经常发生复发,并且不良反应频繁发生,尤其是在老年人口中。目前,甲氨蝶呤被用作保留皮质类固醇的药物,但并没有毒性。因此,将需要一种有效且安全的节省皮质类固醇的药物。正如Kesten及其同事[1]所提到的,至少两个不同的CD4 + T细胞亚群,即Thl 7和Thl细胞,促进了GCA中的血管炎症。 Thl 7细胞对皮质类固醇敏感。但是,Thl细胞对皮质类固醇具有抗药性,而且不受皮质类固醇影响的异常Thl反应仍在继续,从而将GCA确认为长期的,慢性免疫介导的疾病。 γ干扰素是Th1细胞谱系产生的标志性细胞因子。

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