期刊文献+

白细胞介素-26研究进展

Recent advances in interleukin-26
原文传递
导出
摘要 白细胞介素(interleukin,IL)-26最初被认为由T细胞特别是辅助性T细胞17产生。最近的研究发现,自然杀伤细胞、巨噬细胞、成纤维细胞和血管平滑肌细胞也产生IL-26。研究显示,IL-26能够特异性地结合到靶细胞的IL-10R2/IL-20R1受体复合物上,产生特定的胞内信号。除此以外,IL-26还可直接杀灭胞外细菌,并能与死亡细菌DNA或死亡细胞DNA片段结合形成IL-26-DNA复合物,激活浆细胞样树突状细胞Toll样受体9,分泌Ⅰ型干扰素IFN-α,在宿主防御和慢性炎性疾病中发挥重要作用。现对IL-26的结构、来源、受体和功能等进行综述。 Interleukin(IL)-26 was originally thought to be produced by T cells, especially the helper T cells 17. Recent studies have proved that natural killer cells, macrophages, fibroblasts and vascular smooth muscle cells can also produce IL-26. IL-26 has been proved to produce specific intracellular signatures, according to the IL-10 R2/IL-20 R1 receptor complexes. In addition, IL-26 can kill extracellular bacteria and form complexes with bacterial DNA and self-DNA released by dying bacteria and host cells. The IL-26-DNA complexes stimulate the secretion of type I interferon α by plasmacytoid dendritic cells via activation of Toll-like receptor 9. These findings provide insights into an important role of IL-26 in host defense and chronic inflammatory diseases. In the review, we summarized the structure, source, receptor and functions of IL-26.
作者 薛潇春 胡晋红 XUE Xiao-Chun;HU Jin-Hong(Department of Pharmacy, Changhai Hospital, Second Military Medical University, Shanghai 200433, Chin)
出处 《生命科学》 CSCD 北大核心 2018年第5期526-532,共7页 Chinese Bulletin of Life Sciences
基金 国家自然科学基金面上项目(81173130)
关键词 白细胞介素-26 TH17细胞 慢性炎症性疾病 宿主防御 细菌 interleukin (IL)-26 Th17 cells chronic inflammatory diseases host defense bacteria
  • 相关文献

参考文献2

二级参考文献26

  • 1Chartapisak W, Opastiraku S, Willis NS, et al. Prevention and treatment of renal disease in ttenoch-Schonlein purpura:a systematic review [ J ]. Arch Dis in Child,2009,94(2) :132-137.
  • 2Lau KKI, Suzuki H, Novak J, et al. Pathogenesis of Henoch -Schonlein purpura nephritis[ J ]. Pediatr Nephro1,2010,25 (1 ) : 19-26.
  • 3Yoshita K,Tetsu A, Shigeaki M, et al. Clinical remission of Henoch- Schonlein purpura nephritis after a mono therapeutic tonsillectomy [ J ]. Chn Exp Nephro1,2011,15 ( 1 ) : 132-135.
  • 4Warit J, Yasmin E, Hana S, et al. The clinical implicationgs of adult-onset henoch-schonlein purpura [ J]. Clinical and Molecular Allergy, 2011,9 ( 1 ) :9-16.
  • 5Gigante A, Gasperini ML, Afeltra A, et al. Cytokines expression in SLE nephritis [ J ]. Eur Rev Med PharmacolSci ,2011,15 ( 1 ) : 15 -24.
  • 6Joshua M, Brostoff-Gopinath M, Ranganna C, et al. Henoch-Schonlein pur- pura with thrombocythaemia:an abnormality in Smad4 expression? [ J ]. Rheumatol Int ,2009,29 (5) :587-589.
  • 7Bouaziz JD,Calbo S,Maho-Vaillant M,et al. IL-10 produced byac-tivated human B cells regulates CD4 T-cell activation in vitro[ J]. EurJ Immu- no1,2010,40(10) :2686-2691.
  • 8Wong SC, Puaux AL, Chittezhath M, et al. Macrophage polarization to a u- nique phenotype driven by B ceils [ J ]. EurJ [mmunol, 2010,40 ( 8 ) : 2296-2307.
  • 9Raymond PD,Faruk S,Harold D,et al cytokine produced by Thl7 cells [ J ] views ,2010,21 (5) :393-401.
  • 10Interleukin-26 : An IL-10-related Cytokine & Growth Factor Re- Dambacher J,Beigel F,Zitzmann K,et al. The role of the novel Thl7 cy- tokine IL-26inintestinal inflammation [ J ]. Gut, 2009,58 ( 9 ) : 1207- 1217.

共引文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部