A pathogenetic role for IL-21 in primary Sjogren syndrome

被引:33
|
作者
Kwok, Seung-Ki [1 ]
Lee, Jennifer [1 ]
Yu, Di [3 ]
Kang, Kwi Young [1 ]
Cho, Mi-La [2 ]
Kim, Hae-Rim [4 ]
Ju, Ji Hyeon [1 ]
Lee, Sang-Heon [4 ]
Park, Sung-Hwan [1 ]
Kim, Ho-Youn [5 ]
机构
[1] Catholic Univ Korea, Seoul St Marys Hosp, Coll Med, Div Rheumatol,Dept Internal Med, Seoul 137701, South Korea
[2] Catholic Univ Korea, Catholic Res Inst Med Sci, Rheumatism Res Ctr, Seoul 137701, South Korea
[3] Monash Univ, Sch Biomed Sci, Lab Mol Immunomodulat, Clayton, Vic 3800, Australia
[4] Konkuk Univ, Sch Med, Dept Internal Med, Div Rheumatol, Seoul 143729, South Korea
[5] Konkuk Univ, Med Ctr, Seoul 143729, South Korea
基金
新加坡国家研究基金会;
关键词
HELPER T-CELLS; INTERFERON-GAMMA PRODUCTION; SALIVARY-GLANDS; BCL-6; EXPRESSION; CUTTING EDGE; B-CELLS; DIFFERENTIATION; INTERLEUKIN-21; AUTOIMMUNITY; ASSOCIATION;
D O I
10.1038/nrrheum.2014.225
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Advances in our understanding of the pathogenesis of primary Sjogren syndrome (pSS) characterize it as a highly complex process encompassing both the initiation of innate immunity and subsequent adaptive immune responses. IL-21 is receiving attention as a potential key player in the pathogenesis of pSS owing to its pleiotropic effects on the type I interferon signalling pathway, and newly identified roles in generation of follicular and IL-17-producing subtypes of helper T cells, as well as plasma-cell differentiation and B-cell activation. Taking into consideration the diverse biological functions of IL-21 and its clinical relevance to pSS, we propose that this cytokine has a central role in orchestrating the complex immune response in pSS. This hypothesis might provide new insight into the pathogenesis of pSS and facilitate the development of effective therapeutic strategies.
引用
收藏
页码:368 / 374
页数:7
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