CC chemokine receptor 6 (CCR6) in the pathogenesis of systemic lupus erythematosus

被引:9
|
作者
Lee, Adrian Y. S. [1 ,2 ,3 ]
Korner, Heinrich [4 ]
机构
[1] Westmead Hosp, Inst Clin Pathol & Med Res, Hawkesbury Rd, Westmead, NSW 2145, Australia
[2] Univ Sydney, Sydney Med Sch, Westmead, NSW, Australia
[3] Flinders Univ S Australia, Coll Med & Publ Hlth, Bedford Pk, SA, Australia
[4] Anhui Med Univ, Inst Clin Pharmacol, Hefei, Anhui, Peoples R China
来源
IMMUNOLOGY AND CELL BIOLOGY | 2020年 / 98卷 / 10期
关键词
CCL20; CCR6; chemokines; lupus; systemic lupus erythematosus; REGULATORY T-CELLS; TH17; CELLS; PERIPHERAL-BLOOD; B-CELLS; LIGAND; 20; RHEUMATOID-ARTHRITIS; HELPER-CELLS; EXPRESSION; CCL20; IL-17;
D O I
10.1111/imcb.12375
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The CC chemokine receptor 6 (CCR6) and its sole chemokine ligand, CCL20, are an intriguing pair that have been implicated in a growing number of inflammatory, autoimmune and malignant disease processes. Recent observations have also highlighted this chemokine axis in the regulation of humoral immune responses. Through this review article, we explore the emerging links of CCR6-CCL20 with an archetypal autoimmune disease of humoral dysregulation: systemic lupus erythematosus (SLE). CCR6 is expressed prominently on several immune cells involved in the pathogenesis of SLE, such as dendritic cells and T-helper 17 cells. CCR6's expression is correlated with disease activity and serological markers of disease severity, suggesting a possible role in disease pathogenesis. However, there are numerous holes in our understanding of the functions of CCR6 and CCL20, and future studies are required to determine if there are any diagnostic, prognostic or monitoring roles for these important molecules.
引用
收藏
页码:845 / 853
页数:9
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