Ankylosing spondylitis: etiology, pathogenesis, and treatments
Ankylosing spondylitis (AS), a common type of spondyloarthropathy, is a chronic inflammatory autoimmune disease that mainly affects spine joints, causing severe, chronic pain; additionally, in more advanced cases, it can cause spine fusion. Significant progress in its pathophysiology and treatment h...
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Published in | Bone Research Vol. 7; no. 1; pp. 1 - 16 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
05.08.2019
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Abstract | Ankylosing spondylitis (AS), a common type of spondyloarthropathy, is a chronic inflammatory autoimmune disease that mainly affects spine joints, causing severe, chronic pain; additionally, in more advanced cases, it can cause spine fusion. Significant progress in its pathophysiology and treatment has been achieved in the last decade. Immune cells and innate cytokines have been suggested to be crucial in the pathogenesis of AS, especially human leukocyte antigen (HLA)‑B27 and the interleukin‑23/17 axis. However, the pathogenesis of AS remains unclear. The current study reviewed the etiology and pathogenesis of AS, including genome-wide association studies and cytokine pathways. This study also summarized the current pharmaceutical and surgical treatment with a discussion of future potential therapies. |
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AbstractList | Ankylosing spondylitis (AS), a common type of spondyloarthropathy, is a chronic inflammatory autoimmune disease that mainly affects spine joints, causing severe, chronic pain; additionally, in more advanced cases, it can cause spine fusion. Significant progress in its pathophysiology and treatment has been achieved in the last decade. Immune cells and innate cytokines have been suggested to be crucial in the pathogenesis of AS, especially human leukocyte antigen (HLA)‑B27 and the interleukin‑23/17 axis. However, the pathogenesis of AS remains unclear. The current study reviewed the etiology and pathogenesis of AS, including genome-wide association studies and cytokine pathways. This study also summarized the current pharmaceutical and surgical treatment with a discussion of future potential therapies. Ankylosing spondylitis (AS), a common type of spondyloarthropathy, is a chronic inflammatory autoimmune disease that mainly affects spine joints, causing severe, chronic pain; additionally, in more advanced cases, it can cause spine fusion. Significant progress in its pathophysiology and treatment has been achieved in the last decade. Immune cells and innate cytokines have been suggested to be crucial in the pathogenesis of AS, especially human leukocyte antigen (HLA)‑B27 and the interleukin‑23/17 axis. However, the pathogenesis of AS remains unclear. The current study reviewed the etiology and pathogenesis of AS, including genome-wide association studies and cytokine pathways. This study also summarized the current pharmaceutical and surgical treatment with a discussion of future potential therapies.Ankylosing spondylitis (AS), a common type of spondyloarthropathy, is a chronic inflammatory autoimmune disease that mainly affects spine joints, causing severe, chronic pain; additionally, in more advanced cases, it can cause spine fusion. Significant progress in its pathophysiology and treatment has been achieved in the last decade. Immune cells and innate cytokines have been suggested to be crucial in the pathogenesis of AS, especially human leukocyte antigen (HLA)‑B27 and the interleukin‑23/17 axis. However, the pathogenesis of AS remains unclear. The current study reviewed the etiology and pathogenesis of AS, including genome-wide association studies and cytokine pathways. This study also summarized the current pharmaceutical and surgical treatment with a discussion of future potential therapies. |
Author | He, Xuxia Weng, Xisheng Zhu, Wei Zhang, Linjie Chen, Di Qiu, Guixing Cao, Xu Wang, Xiao Cheng, Kaiyuan |
Author_xml | – sequence: 1 givenname: Wei surname: Zhu fullname: Zhu, Wei organization: Department of Orthopedics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College – sequence: 2 givenname: Xuxia surname: He fullname: He, Xuxia organization: Department of Clinical Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College – sequence: 3 givenname: Kaiyuan surname: Cheng fullname: Cheng, Kaiyuan organization: Department of Orthopedics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College – sequence: 4 givenname: Linjie surname: Zhang fullname: Zhang, Linjie organization: Department of Orthopedics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College – sequence: 5 givenname: Di surname: Chen fullname: Chen, Di organization: Department of Orthopedic Surgery, Rush University Medical Center – sequence: 6 givenname: Xiao orcidid: 0000-0001-6395-706X surname: Wang fullname: Wang, Xiao organization: Department of Orthopedic Surgery, School of Medicine, Johns Hopkins University – sequence: 7 givenname: Guixing surname: Qiu fullname: Qiu, Guixing organization: Department of Orthopedics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College – sequence: 8 givenname: Xu surname: Cao fullname: Cao, Xu email: xcao11@jhmi.edu organization: Department of Orthopedic Surgery, School of Medicine, Johns Hopkins University – sequence: 9 givenname: Xisheng surname: Weng fullname: Weng, Xisheng email: xshweng@medmail.com.cn organization: Department of Orthopedics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College |
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