Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Sep;236(9):6090-6100.
doi: 10.1002/jcp.30313. Epub 2021 Feb 8.

Osteoimmunological insights into the pathogenesis of ankylosing spondylitis

Affiliations
Review

Osteoimmunological insights into the pathogenesis of ankylosing spondylitis

Lifei Liu et al. J Cell Physiol. 2021 Sep.

Abstract

Ankylosing spondylitis (AS) is inflammatory arthritis predominantly affecting the spine, which is involved in the disorders of both immune and skeletal systems. The exact pathogenesis of AS is not fully understood. Osteoimmunology is a new subject of study in inflammatory arthritis, in particular the pathogenic events involved in the cross-regulation of both skeletal and immune systems. In this review, we discuss osteoimmunological and pathological changes of AS in the spine that are characterized by altered osteogenesis and osteolytic bone destruction, accompanied by the changes of the immune system. It was revealed that bone cells like mesenchymal stem cells, osteoblast, and osteoclast in crossing talking with immune cells such as T cells, B cells coregulate to the pathogenesis of AS. Further, an array of cytokines and molecules expressed by both skeletal and immune systems contribute to these complex interplays. Understanding the cellular and molecular mechanisms underlying the pathogenesis of AS will lay a foundation for the exploration of the potential new treatment to AS.

Keywords: B cell; T cell; ankylosing spondylitis; osteoimmunology; skeletal system.

PubMed Disclaimer

References

REFERENCES

    1. Adamopoulos, I. E. (2018). Inflammation in bone physiology and pathology. Current Opinion in Rheumatology, 30(1), 59-64. https://doi.org/10.1097/BOR.0000000000000449
    1. Adamopoulos, I. E. , & Bowman, E. P. (2008). Immune regulation of bone loss by Th17 cells. Arthritis Research & Therapy, 10(5), 225. https://doi.org/10.1186/ar2502
    1. Adamopoulos, I. E. , Chao, C. , Geissler, R. , Laface, D. , Blumenschein, W. , Iwakura, Y. , McClanahan, T. , & Bowman, E. P. (2010). Interleukin-17A upregulates receptor activator of NF-kappaB on osteoclast precursors. Arthritis Research & Therapy, 12(1), R29. https://doi.org/10.1186/ar2936
    1. Akhtari, M. , Zargar, S. J. , Mahmoudi, M. , Vojdanian, M. , Rezaeimanesh, A. , & Jamshidi, A. (2018). Ankylosing spondylitis monocyte-derived macrophages express increased level of A2A adenosine receptor and decreased level of ectonucleoside triphosphate diphosphohydrolase-1 (CD39), A1 and A2B adenosine receptors. Clinical Rheumatology, 37(6), 1589-1595. https://doi.org/10.1007/s10067-018-4055-9
    1. Akiyama, K. , Chen, C. , Wang, D. , Xu, X. , Qu, C. , Yamaza, T. , Cai, T. , Chen, W. , Sun, L. , & Shi, S. (2012). Mesenchymal-stem-cell-induced immunoregulation involves FAS-ligand-/FAS-mediated T cell apoptosis. Cell Stem Cell, 10(5), 544-555. https://doi.org/10.1016/j.stem.2012.03.007

Publication types

LinkOut - more resources