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The poor recovery of neuromyelitis optica spectrum disorder is associated with a lower level of CXCL12 in the human brain

  • Hao Kang
  • , Shanshan Cao
  • , Tingjun Chen
  • , Zhaocai Jiang
  • , Zihao Liu
  • , Zhaohui Li
  • , Yangang Wei
  • , Nanping Ai
  • , Quangang Xu
  • , Qing Lin
  • , Shihui Wei
  • The Chinese People's Liberation Army General Hospital
  • Beijing Longfu Hospital
  • Dongzhimen Hospital of Beijing University of Chinese Medicine
  • Bioori Translational Medicine Center
  • University of Texas at Arlington

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Neuromyelitis optica spectrum disorders (NMOSDs) are blindness-causing neuritis. In NMOSD patients, NMO-IgG evokes astrocytopathy that in turn causes demyelination. While measurement of NMO-IgG titer will help neurologists make the diagnosis of NMOSDs, it is not sufficient to evaluate the severity of astrocytopathy. In this study, we compared the different levels of an astrocyte biomarker in cerebrospinal fluid of NMOSD patients with good or poor recovery, and then linked their differences to the changes in remyelinating promoter (CXCL12) levels. Our results indicate that NMO-IgG down-regulated CXCL12 and impaired the remyelinating process, this may be a mechanism contributing to the poor recovery of NMOSDs.

Original languageEnglish
Pages (from-to)56-61
Number of pages6
JournalJournal of Neuroimmunology
Volume289
DOIs
StatePublished - 15 Dec 2015
Externally publishedYes

Keywords

  • Aquaporin 4 (AQP4)
  • CXC-motif ligand 12 (CXCL12)
  • Glial fibrillary acidic protein (GFAP)
  • Neuromyelitis optica spectrum disorders (NMOSDs)
  • Tumor necrosis factor α (TNFα)

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