Mechanistic target of rapamycin (mTOR): a potential new therapeutic target for rheumatoid arthritis

被引:14
|
作者
Zhang, Fen [1 ,2 ,3 ]
Cheng, Ting [1 ,2 ,3 ]
Zhang, Sheng-Xiao [1 ,2 ,3 ]
机构
[1] Shanxi Med Univ, Hosp 2, Dept Rheumatol, 382 Wuyi Rd, Taiyuan 030001, Shanxi, Peoples R China
[2] Shanxi Prov Key Lab Rheumatism Immune Microecol, Taiyuan, Shanxi, Peoples R China
[3] Shanxi Med Univ, Key Lab Cellular Physiol, Minist Educ, Taiyuan, Shanxi, Peoples R China
关键词
Rheumatoid arthritis; mTOR; Treatment; FIBROBLAST-LIKE SYNOVIOCYTES; N-ACETYL CYSTEINE; CRYO-EM STRUCTURE; T-CELLS; MAMMALIAN TARGET; B-CELLS; DENDRITIC CELLS; REGULATORY T; IN-VITRO; IMMUNE-RESPONSE;
D O I
10.1186/s13075-023-03181-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rheumatoid arthritis (RA) is an autoimmune disease characterized by systemic synovitis and bone destruction. Proinflammatory cytokines activate pathways of immune-mediated inflammation, which aggravates RA. The mechanistic target of rapamycin (mTOR) signaling pathway associated with RA connects immune and metabolic signals, which regulates immune cell proliferation and differentiation, macrophage polarization and migration, antigen presentation, and synovial cell activation. Therefore, therapy strategies targeting mTOR have become an important direction of current RA treatment research. In the current review, we summarize the biological functions of mTOR, its regulatory effects on inflammation, and the curative effects of mTOR inhibitors in RA, thus providing references for the development of RA therapeutic targets and new drugs.
引用
收藏
页数:13
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