Ankylosing spondylitis: From pathogenesis to therapy

被引:4
作者
Wei, Yuxiao [1 ]
Zhang, Shuqiong [1 ]
Shao, Fenli [2 ]
Sun, Yang [1 ]
机构
[1] Nanjing Univ, Chem & Biomed Innovat Ctr ChemBIC, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, 163 Xianlin Ave, Nanjing 210023, Jiangsu, Peoples R China
[2] Nanjing Univ Chinese Med, State Key Lab Technol Chinese Med Pharmaceut Proc, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
Ankylosing spondylitis; Pathogenesis; Treatment; Therapeutic targets; NECROSIS-FACTOR INHIBITORS; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; UNFOLDED PROTEIN RESPONSE; INNATE LYMPHOID-CELLS; DELTA-T-CELLS; AXIAL SPONDYLOARTHRITIS; RADIOGRAPHIC PROGRESSION; PERIPHERAL-BLOOD; DOUBLE-BLIND; TGF-BETA;
D O I
10.1016/j.intimp.2024.113709
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ankylosing spondylitis (AS) is an autoimmune rheumatic disease that primarily affects the axial joints, with its etiology complex and still not fully understood. The unknown pathogenesis of AS limits the development of treatment strategies, so keeping up-to-date with the current research on AS can help in searching for potential therapeutic targets. In addition to the classic HLA-B27 genetic susceptibility and Th17-related inflammatory signals, increasing research is focusing on the influence of autoantigen-centered autoimmune responses and bone stromal cells on the onset of AS. Autoantigens derived from gut microbiota and preferential TCR both exacerbate the autoimmune response in patients with AS. Furthermore, dysregulated bone metabolism also promotes pathological new bone formation in AS. Current treatments approved for AS almost focus on the management of inflammation with inconsistent treatment results due to the heterogeneity of patients. In this review, we systematically summarized various pathogenesis and management of AS, meanwhile discussed the underlying risk factors and potential therapeutic targets.
引用
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页数:20
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共 289 条
[1]   Risk of Subsequent Infection Among Patients Receiving Tumor Necrosis Factor Inhibitors and Other Disease-Modifying Antirheumatic Drugs [J].
Accortt, Neil A. ;
Bonafede, Machaon M. ;
Collier, David H. ;
Iles, Jan ;
Curtis, Jeffrey R. .
ARTHRITIS & RHEUMATOLOGY, 2016, 68 (01) :67-76
[2]   Interleukin-23 promotes a distinct CD4 T cell activation state characterized by the production of interleukin-17 [J].
Aggarwal, S ;
Ghilardi, N ;
Xie, MH ;
de Sauvage, FJ ;
Gurney, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (03) :1910-1914
[3]   Genetic associations and functional characterization of M1 aminopeptidases and immune-mediated diseases [J].
Agrawal, N. ;
Brown, M. A. .
GENES AND IMMUNITY, 2014, 15 (08) :521-527
[4]   Salmonella exploits HLA-B27 and host unfolded protein responses to promote intracellular replication [J].
Antoniou, Antony Nicodemus ;
Lenart, Lzabela ;
Kriston-Vizi, Janos ;
Lwawaki, Takao ;
Turmaine, Mark ;
McHugh, Kirsty ;
Ali, Sadfer ;
Blake, Neil ;
Bowness, Paul ;
Bajaj-Elliott, Mona ;
Gould, Keith ;
Nesbeth, Darren ;
Powis, Simon J. .
ANNALS OF THE RHEUMATIC DISEASES, 2019, 78 (01) :74-82
[5]   Paradoxical psoriasis following anti-TNF therapy in ankylosing spondylitis: A population-based cohort study [J].
Bae, Jung Min ;
Kwon, Hyuck Sun ;
Kim, Gyong Moon ;
Park, Kyung-Su ;
Kim, Ki-Jo .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2018, 142 (03) :1001-1003
[6]   Risankizumab, an IL-23 inhibitor, for ankylosing spondylitis: results of a randomised, double-blind, placebo-controlled, proof-of-concept, dose-finding phase 2 study [J].
Baeten, Dominique ;
Ostergaard, Mikkel ;
Wei, James Cheng-Chung ;
Sieper, Joachim ;
Jarvinen, Pentti ;
Tam, Lai-Shan ;
Salvarani, Carlo ;
Kim, Tae-Hwan ;
Solinger, Alan ;
Datsenko, Yakov ;
Pamulapati, Chandrasena ;
Visvanathan, Sudha ;
Hall, David B. ;
Aslanyan, Stella ;
Scholl, Paul ;
Padula, Steven J. .
ANNALS OF THE RHEUMATIC DISEASES, 2018, 77 (09) :1295-1302
[7]   Secukinumab, an Interleukin-17A Inhibitor, in Ankylosing Spondylitis [J].
Baeten, Dominique ;
Sieper, Joachim ;
Braun, Juergen ;
Baraliakos, Xenofon ;
Dougados, Maxime ;
Emery, Paul ;
Deodhar, Atul ;
Porter, Brian ;
Martin, Ruvie ;
Andersson, Mats ;
Mpofu, Shephard ;
Richards, Hanno B. .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (26) :2534-2548
[8]   Dkk (Dickkopf) Proteins Emerging New Players in Atherosclerosis [J].
Baetta, Roberta ;
Banfi, Cristina .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2019, 39 (07) :1330-1342
[9]   Which spinal lesions are associated with new bone formation in patients with ankylosing spondylitis treated with anti-TNF agents? A long-term observational study using MRI and conventional radiography [J].
Baraliakos, X. ;
Heldmann, F. ;
Callhoff, J. ;
Listing, J. ;
Appelboom, T. ;
Brandt, J. ;
Van den Bosch, F. ;
Breban, M. ;
Burmester, G. R. ;
Dougados, M. ;
Emery, P. ;
Gaston, H. ;
Grunke, M. ;
Van Der Horst-Bruinsma, I. E. ;
Landewe, R. ;
Leirisalo-Repo, M. ;
Sieper, J. ;
De Vlam, K. ;
Pappas, D. ;
Kiltz, U. ;
Van Der Heijde, D. ;
Braun, J. .
ANNALS OF THE RHEUMATIC DISEASES, 2014, 73 (10) :1819-1825
[10]   Bimekizumab treatment in patients with active axial spondyloarthritis: 52-week efficacy and safety from the randomised parallel phase 3 BE MOBILE 1 and BE MOBILE 2 studies [J].
Baraliakos, Xenofon ;
Deodhar, Atul ;
van der Heijde, Desiree ;
Magrey, Marina ;
Maksymowych, Walter P. ;
Tomita, Tetsuya ;
Xu, Huji ;
Massow, Ute ;
Fleurinck, Carmen ;
Ellis, Alicia M. ;
Vaux, Thomas ;
Shepherd-Smith, Julie ;
Marten, Alexander ;
Gensler, Lianne S. .
ANNALS OF THE RHEUMATIC DISEASES, 2024, 83 (02) :199-213