Arthritis Res Ther. 2011 Jun 24;13(3):115. doi: 10.1186/ar3351.
The past decade has witnessed significant progress in revealing an important role for IL-17 in the pathogenesis of several immune-mediated inflammatory diseases. Recent studies have provided new insights into the cellular source of IL-17, originally identified as the signature cytokine of a distinct CD4(+) T-cell subset known as Th17. Accumulating evidence suggests that the majority of the IL-17 released in inflammatory arthritis is produced by innate immune cells rather than T cells. Understanding molecular mechanisms behind these early innate immune responses will be the key to designing rational therapies targeting these important inflammatory pathways.
过去十年见证了在揭示白细胞介素-17 (IL-17) 在几种免疫介导的炎症性疾病发病机制中的重要作用方面取得的重大进展。最近的研究为 IL-17 的细胞来源提供了新的见解,最初被确定为一种称为 Th17 的独特 CD4(+) T 细胞亚群的特征细胞因子。越来越多的证据表明,在炎症性关节炎中释放的大多数白细胞介素-17 是由先天免疫细胞而不是 T 细胞产生的。了解这些早期先天免疫反应背后的分子机制将是设计针对这些重要炎症途径的合理治疗方法的关键。