Glial Fibrillary Acidic Protein (GFAP) Autoimmunity in the Setting of Seropositive Rheumatoid Arthritis Treated with Etanercept

Kelsey M. Smith, Shreyasee Amin, Lyell K. Jones, Daniel H. Lachance, Eoin P. Flanagan, Mark E. Jentoft, Orhun H. Kantarci

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Introduction:Glial fibrillary acidic protein (GFAP) immunoglobulin G is a recently discovered biomarker of an autoimmune central nervous system disorder characterized by a steroid-responsive meningoencephalomyelitis.Case Report:A 63-year-old man with rheumatoid arthritis on etanercept presented with steroid-responsive subacute encephalopathy and foot drop. Brain and sural nerve biopsies demonstrated a T-cell perivascular infiltrate. Cerebrospinal fluid studies 18 months into the course of the illness demonstrated a GFAP antibody on mouse tissue immunofluorescence confirmed by cell-based assay. The patient was treated with steroids and cyclophosphamide leading to resolution of his symptoms.Conclusion:This case expands on the previously reported cases of GFAP immunoglobulin G autoimmunity by describing an associated inflammatory large fiber peripheral neuropathy.

Original languageEnglish (US)
Pages (from-to)152-154
Number of pages3
JournalNeurologist
Volume24
Issue number5
DOIs
StatePublished - Sep 1 2019

Keywords

  • GFAP
  • TNF-inhibitor
  • encephalopathy
  • neuroimmunology
  • neuropathy

ASJC Scopus subject areas

  • Clinical Neurology

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