Absence of antibodies against KIR4.1 in multiple sclerosis: A three-technique approach and systematic review

PLoS One. 2017 Apr 17;12(4):e0175538. doi: 10.1371/journal.pone.0175538. eCollection 2017.

Abstract

Introduction: Antibodies targeting the inward-rectifying potassium channel KIR4.1 have been associated with multiple sclerosis (MS) but studies using diverse techniques have failed to replicate this association. The detection of these antibodies is challenging; KIR4.1 glycosylation patterns and the use of diverse technical approaches may account for the disparity of results. We aimed to replicate the association using three different approaches to overcome the technical limitations of a single technique. We also performed a systematic review to examine the association of anti-KIR4.1 antibodies with MS.

Methods: Serum samples from patients with MS (n = 108) and controls (n = 77) were tested for the presence of anti-KIR4.1 antibodies using three methods: 1) by ELISA with the low-glycosylated fraction of recombinant KIR4.1 purified from transfected HEK293 cells according to original protocols; 2) by immunocytochemistry using KIR4.1-transfected HEK293 cells; and 3) by immunocytochemistry using the KIR4.1.-transfected MO3.13 oligodendrocyte cell line. We developed a systematic review and meta-analysis of the association of anti-KIR4.1 antibodies with MS according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.

Results: We did not detect anti-KIR4.1 antibodies in the MS patients or in controls using ELISA. Neither did we detect any significant reactivity against the antigen on the cell surface using the KIR4.1-transfected HEK293 cells or the KIR4.1-transfected MO3.13 cells. We included 13 prospective controlled studies in the systematic review. Only three studies showed a positive association between anti-KIR4.1 and MS. Clinical and statistical heterogeneity between studies precluded meta-analysis of their results.

Conclusion: We found no association between anti-KIR4.1 antibody positivity and MS. Although this lack of replication may be due to technical limitations, evidence from our study and others is mounting against the role of KIR4.1 as a relevant MS autoantigen.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antibodies / immunology*
  • Autoantigens / immunology
  • Cell Line
  • Female
  • Glycosylation
  • HEK293 Cells
  • Humans
  • Male
  • Middle Aged
  • Multiple Sclerosis / immunology*
  • Potassium Channels, Inwardly Rectifying / immunology*
  • Prospective Studies
  • Young Adult

Substances

  • Antibodies
  • Autoantigens
  • Kcnj10 (channel)
  • Potassium Channels, Inwardly Rectifying

Grants and funding

The experimental study has been funded with an unrestricted grant from Novartis Spain. LQ is supported by the JR13/00014 of the Instituto de Salud Carlos III, Ministry of Economy and Innovation, Spain. The systematic review was performed independently and was not funded by the leading funding source.