Frontiers in Immunology (Aug 2022)

Serological biomarkers in autoimmune GFAP astrocytopathy

  • Cong-Cong Fu,
  • Cong-Cong Fu,
  • Lu Huang,
  • Lu Huang,
  • Lu-Fen Xu,
  • Lu-Fen Xu,
  • Li-Hong Jiang,
  • Li-Hong Jiang,
  • Hui-Lu Li,
  • Hui-Lu Li,
  • Sha Liao,
  • Sha Liao,
  • Jiajia Yue,
  • Jiajia Yue,
  • Chun Lian,
  • Chun Lian,
  • Xin-Guang Yang,
  • Xin-Guang Yang,
  • Xin-Guang Yang,
  • You-Ming Long,
  • You-Ming Long

DOI
https://doi.org/10.3389/fimmu.2022.957361
Journal volume & issue
Vol. 13

Abstract

Read online

Autoimmune glial fibrillary acidic protein astrocytopathy (GFAP-A) is a newly defined meningoencephalomyelitis. The pathogenesis of GFAP-A is not well understood. The present study measured the expression levels of 200 serological cytokines in GFAP-A patients, NMOSD patients and healthy controls (HCs). The correlations between serum cytokine levels and clinical information in GFAP-A patients were analyzed. A total of 147 serological proteins were differentially expressed in GFAP-A patients compared to HCs, and 33 of these proteins were not observed in NMOSD patients. Serum levels of EG-VEGF negatively correlated with GFAP antibody titers, MIP-3 alpha positively correlated with clinical severity in GFAP-A patients, and LIGHT positively correlated with WBC counts and protein levels in the CSF of GFAP-A patients. These results suggest that GFAP and AQP4 astrocytopathy share some common pathology related to TNF signaling. Serum MIP 3 alpha may be a biomarker to assess clinical severity and a potential target for therapy of autoimmune GFAP astrocytopathy.

Keywords