Antibody response against gastrointestinal antigens in demyelinating diseases of the central nervous system

M. Banati, P. Csecsei, E. Koszegi, H. H. Nielsen, G. Suto, L. Bors, A. Trauninger, T. Csepany, C. Rozsa, G. Jakab, T. Molnar, A. Berthele, S. R. Kalluri, T. Berki, Z. Illes

Research output: Contribution to journalArticlepeer-review

55 Scopus citations

Abstract

Background: Antibodies against gastrointestinal antigens may indicate altered microbiota and immune responses in the gut. Recent experimental data suggest a connection between gastrointestinal immune responses and CNS autoimmunity. Methods: Antibodies against gliadin, tissue transglutaminase (tTG), intrinsic factor (IF), parietal cells (PC) and Saccharomyces cerevisiae (ASCA) were screened in the sera of 45 patients with AQP4-seropositive neuromyelitis optica (NMO) and NMO spectrum diseases (NMO/NMO-SD), 17 patients with AQP4-seronegative NMO, 85 patients with clinically definite multiple sclerosis (MS), and 48 healthy controls (HC). Results: Thirty-seven percentages of patients with AQP4-seropositive NMO/NMO-SD and 28% of patients with MS had at least one particular antibody in contrast to 8% of HC (P < 0.01, respectively). Antibodies were most common (46%) in AQP4-seropositive myelitis (P = 0.01 versus HS, P = 0.05 versus MS). Anti-gliadin and ASCA were more frequent in the AQP4-seropositive NMO-spectrum compared to controls (P = 0.01 and P < 0.05, respectively). Conclusion: Antibody responses against gastrointestinal antigens are common in MS and AQP4-seropositive NMO/NMO-SD, especially in longitudinally extensive myelitis.

Original languageEnglish
Pages (from-to)1492-1495
Number of pages4
JournalEuropean Journal of Neurology
Volume20
Issue number11
DOIs
StatePublished - Nov 2013

Keywords

  • Anti-Saccharomyces cerevisiae
  • Aquaporin 4
  • Gliadin
  • Intrinsic factor
  • Multiple sclerosis
  • Myelitis
  • Neuromyelitis optica
  • Optic neuritis
  • Parietal cell
  • Transglutaminase

Fingerprint

Dive into the research topics of 'Antibody response against gastrointestinal antigens in demyelinating diseases of the central nervous system'. Together they form a unique fingerprint.

Cite this