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REVIEW article

Front. Immunol.

Sec. Autoimmune and Autoinflammatory Disorders: Autoinflammatory Disorders

Volume 16 - 2025 | doi: 10.3389/fimmu.2025.1633318

Decoding the Inflammatory-Osteogenic Axis in Ankylosing Spondylitis: Mechanisms, Dysregulation, and Emerging Therapeutic Interventions

Provisionally accepted
  • 1Jahangirnagar University, Savar, Bangladesh
  • 2Hallym University, Chuncheon-si, Republic of Korea
  • 3Kangwon National University, Chuncheonsi, Republic of Korea

The final, formatted version of the article will be published soon.

Ankylosing spondylitis (AS) is a chronic autoimmune disorder that primarily affects young people, with an incidence of approximately 1% worldwide. Although genetic and environmental factors have been implicated in the pathogenesis of AS, the etiology of this condition remains unclear. Observations indicate that individuals possessing the human leukocyte antigen (HLA)-B27 allele exhibit elevated risk factors, as any mutation within this gene could potentially result in the development of AS in the future. However, it is interesting to note that many AS patients do not carry this gene, inferring the involvement of other genetic and nongenetic factors in the development of the disease. As the exact mechanisms remain unknown, no target-specific treatments exist to cure AS. Nonetheless, some treatment regimens have been devised to alleviate AS symptoms. This review thoroughly examines the molecular mechanisms implicated in AS, encompassing insights into the significance of pivotal biomarkers, such as extracellular matrix metabolites, immune cell dynamics, gut microbiota interactions, the Wnt signaling pathway, and its inhibitors.Furthermore, a thorough evaluation of the different mouse models used in AS research has been reviewed, which is crucial for understanding disease pathways and assessing treatment methods. In addition, significant progress in developing effective treatment strategies for AS and drugs available for the treatment and in clinical trials for treating AS have, along with drugs available for treatment and ongoing clinical trials, has been summarized. A comprehensive understanding of experimental mice mouse models, along with insights into molecular mechanisms and biomarkers for AS, could aid researchers and physicians in discovering new treatment strategies for this challenging condition.

Keywords: ankylosing spondylitis, HLA-B27, PGISp mouse, ERAP1 gene, therapeutic targets

Received: 22 May 2025; Accepted: 22 Aug 2025.

Copyright: © 2025 Parvin, Sharma, Hasan, Sharma, Shawan, Seo, Hasan and Lee. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Md. Mahmudul Hasan, Jahangirnagar University, Savar, Bangladesh
Sang Soo Lee, Hallym University, Chuncheon-si, Republic of Korea

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