Targeting tumor necrosis factor receptors in ankylosing spondylitis

被引:44
|
作者
Lata, Michal [1 ]
Hettinghouse, Aubryanna S. [1 ]
Liu, Chuan-ju [1 ,2 ]
机构
[1] NYU, Med Ctr, Hosp Joint Dis, Dept Orthoped Surg, Room 1608,301 East 17th St, New York, NY 10003 USA
[2] NYU, Sch Med, Dept Cell Biol, New York, NY 10016 USA
关键词
ankylosing spondylitis; TNFR1; TNFR2; TNF inhibitors; progranulin; MESENCHYMAL STEM-CELLS; SOCIETY CLASSIFICATION CRITERIA; FACTOR-ALPHA; TNF-ALPHA; OSTEOBLAST DIFFERENTIATION; GROWTH-FACTOR; OSTEOGENIC DIFFERENTIATION; AXIAL SPONDYLOARTHRITIS; TRANSGENIC MICE; ADIPOSE-TISSUE;
D O I
10.1111/nyas.13933
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Over the past two decades, considerable advances in our understanding of inflammatory and immune pathways have allowed for the growing use of targeted biologic therapy. Most notably, the introduction of tumor necrosis factor (TNF) inhibitors has dramatically changed the management of autoimmune inflammatory disorders, including ankylosing spondylitis (AS). Despite the efficacy of TNF inhibitors documented in multiple clinical trials, anti-TNF therapy in AS is far from foolproof; it is associated with serious adverse effects and limited response to therapy in some patients. Moreover, specific questions regarding the role of TNF as a mediator of AS remain unanswered. Therefore, additional efforts are needed in order to better understand the role of TNF in the pathogenesis of AS and to develop safer and more effective treatment strategies. The purpose of this review is to better the understanding of the physiologic and pathogenic roles of TNF signaling in the course of AS. Relevant TNF biology and novel approaches to TNF blockade in AS are discussed.
引用
收藏
页码:5 / 16
页数:12
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