» Articles » PMID: 33977094

Anti-IL-17 Agents in the Treatment of Axial Spondyloarthritis

Overview
Publisher Dove Medical Press
Date 2021 May 12
PMID 33977094
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Axial spondyloarthritis (axSpA) describes a group of chronic inflammatory rheumatic diseases primarily involving the axial skeleton. IL-17 is involved in the pathogenesis of numerous inflammatory diseases, including inflammatory arthritis. Until a few years ago, the only biological agents licensed for the treatment of axSpA and nr-axSpA were TNF inhibitors. However, as some patients did not respond to TNF inhibition or experienced secondary failure, the introduction of the first two IL-17 inhibitors (secukinumab [SEC] and ixekizumab [IXE]) has extended the treatment options, and there are now three others (bimekizumab, brodalumab and netakimab) in various stages of clinical development. The last ten years have seen the development of a number of therapeutic recommendations that aimed at improving the management of axSpA patients. The aim of this narrative review of the published literature concerning the role of IL-17 in the pathogenesis of SpA, and the role of IL-17 inhibitors in the treatment of axSpA, is to provide a comprehensive picture of the clinical efficacy and safety of the drugs themselves, and the treatment strategies recommended in the international guidelines.

Citing Articles

A systematic review of the role of interleukin-17 inhibitors in bullous pemphigoid: therapeutic and paradoxical effects.

Heidari N, Hosseini S, Heidari A, Ghane Y, Daneshpazhooh M, Mahmoudi H Arch Dermatol Res. 2025; 317(1):544.

PMID: 40067544 DOI: 10.1007/s00403-025-04052-x.


Progress in targeted therapy for ankylosing spondylitis: A review.

Wang J, Lou W, Li Y, Jiang Y, Jiang X, Yang L Medicine (Baltimore). 2024; 103(48):e40742.

PMID: 39612456 PMC: 11608699. DOI: 10.1097/MD.0000000000040742.


.

Zrour S, Dridi A, Grassa R, Ben Chekaya N, Bejia I Tunis Med. 2024; 102(11):910-915.

PMID: 39564635 PMC: 11668151. DOI: 10.62438/tunismed.v102i11.5059.


Ixekizumab Treatment Patterns and Health Care Resource Utilization Among Patients with Axial Spondyloarthritis: A Retrospective United States Claims Database Study.

Danve A, Vadhariya A, Lisse J, Cholayil A, Bansal N, Bello N Rheumatol Ther. 2024; 11(5):1333-1345.

PMID: 39162898 PMC: 11422398. DOI: 10.1007/s40744-024-00710-0.


Differentiation and regulation of CD4 T cell subsets in Parkinson's disease.

Sun X, Gu R, Bai J Cell Mol Life Sci. 2024; 81(1):352.

PMID: 39153043 PMC: 11335276. DOI: 10.1007/s00018-024-05402-0.


References
1.
Lubberts E, Koenders M, van den Berg W . The role of T-cell interleukin-17 in conducting destructive arthritis: lessons from animal models. Arthritis Res Ther. 2005; 7(1):29-37. PMC: 1064899. DOI: 10.1186/ar1478. View

2.
Hazenberg M, Spits H . Human innate lymphoid cells. Blood. 2014; 124(5):700-9. DOI: 10.1182/blood-2013-11-427781. View

3.
Ward M, Deodhar A, Gensler L, Dubreuil M, Yu D, Khan M . 2019 Update of the American College of Rheumatology/Spondylitis Association of America/Spondyloarthritis Research and Treatment Network Recommendations for the Treatment of Ankylosing Spondylitis and Nonradiographic Axial Spondyloarthritis. Arthritis Rheumatol. 2019; 71(10):1599-1613. PMC: 6764882. DOI: 10.1002/art.41042. View

4.
Papp K, Leonardi C, Menter A, Ortonne J, Krueger J, Kricorian G . Brodalumab, an anti-interleukin-17-receptor antibody for psoriasis. N Engl J Med. 2012; 366(13):1181-9. DOI: 10.1056/NEJMoa1109017. View

5.
Schwarzenberger P, La Russa V, Miller A, Ye P, Huang W, Zieske A . IL-17 stimulates granulopoiesis in mice: use of an alternate, novel gene therapy-derived method for in vivo evaluation of cytokines. J Immunol. 1998; 161(11):6383-9. View