Human Endogenous Retrovirus and Neuroinflammation in Chronic Inflammatory Demyelinating Polyradiculoneuropathy

EBioMedicine. 2016 Apr:6:190-198. doi: 10.1016/j.ebiom.2016.03.001. Epub 2016 Mar 10.

Abstract

Background: Human endogenous retroviruses HERV-W encode a pro-inflammatory protein, named MSRV-Env from its original identification in Multiple Sclerosis. Though not detected in various neurological controls, MSRV-Env was found in patients with chronic inflammatory demyelinating polyradiculoneuropathies (CIDPs). This study investigated the expression of MSRV in CIDP and evaluated relevant MSRV-Env pathogenic effects.

Methods: 50 CIDP patients, 19 other neurological controls (ONDs) and 65 healthy blood donors (HBDs) were recruited from two different countries. MSRV-env and -pol transcripts, IL6 and CXCL10 levels were quantified from blood samples. MSRV-Env immunohistology was performed in distal sensory nerves from CIDP and neurological controls biopsies. MSRV-Env pathogenic effects and mode of action were assayed in cultured primary human Schwann cells (HSCs).

Findings: In both cohorts, MSRV-env and -pol transcripts, IL6 positivity prevalence and CXCL10 levels were significantly elevated in CIDP patients when compared to HBDs and ONDs (statistically significant in all comparisons). MSRV-Env protein was detected in Schwann cells in 5/7 CIDP biopsies. HSC exposed to or transfected with MSRV-env presented a strong increase of IL6 and CXCL10 transcripts and protein secretion. These pathogenic effects on HSC were inhibited by GNbAC1, a highly specific and neutralizing humanized monoclonal antibody targeting MSRV-Env.

Interpretation: The present study showed that MSRV-Env may trigger the release of critical immune mediators proposed as instrumental factors involved in the pathophysiology of CIDP. Significant MSRV-Env expression was detected in a significant proportion of patients with CIDP, in which it may play a role according to its presently observed effects on Schwann cells along with previously known effects on immune cells. Experimental results also suggest that a biomarker-driven therapeutic strategy targeting this protein with a neutralizing antibody such as GNbAC1 may offer new perspectives for treating CIDP patients with positive detection of MSRV-Env expression.

Funding: Geneuro-Innovation, France.

Keywords: CIDP; Endogenous retrovirus; GNbAC1; HERV; HERV-W; MSRV; Peripheral neuropathies; Schwann cell.

MeSH terms

  • Adult
  • Aged
  • Antibodies, Monoclonal, Humanized / pharmacology
  • Cell Line
  • Chemokine CXCL10 / genetics*
  • Endogenous Retroviruses / genetics
  • Endogenous Retroviruses / immunology
  • Endogenous Retroviruses / pathogenicity*
  • Female
  • France
  • Gene Products, env / genetics*
  • Gene Products, pol / genetics
  • Humans
  • Interleukin-6 / genetics*
  • Male
  • Middle Aged
  • Polyradiculoneuropathy, Chronic Inflammatory Demyelinating / genetics
  • Polyradiculoneuropathy, Chronic Inflammatory Demyelinating / immunology*
  • Polyradiculoneuropathy, Chronic Inflammatory Demyelinating / virology
  • Schwann Cells / drug effects
  • Schwann Cells / virology
  • Young Adult

Substances

  • Antibodies, Monoclonal, Humanized
  • CXCL10 protein, human
  • Chemokine CXCL10
  • Gene Products, env
  • Gene Products, pol
  • IL6 protein, human
  • Interleukin-6
  • temelimab