Cross-immunogenicity: antibodies to infliximab in Remicade-treated patients with IBD similarly recognise the biosimilar Remsima

Gut. 2016 Jul;65(7):1132-8. doi: 10.1136/gutjnl-2015-309290. Epub 2015 Apr 20.

Abstract

Objective: The cross-immunogenicity of the recently approved infliximab-biosimilar Remsima (CT-P13) with the originator drug Remicade is still unknown.

Design: Sera of patients with IBD with or without measurable anti-Remicade antibodies to infliximab (ATI) were tested for their cross-reactivity to two batches of Remsima. Experiments were repeated after deglycosylation of Remicade/Remsima, IgG purification, excipients' dialysis and monomer purification by size exclusion chromatography. Anti-Remicade antibodies were tested for their functional inhibition of TNF-α binding by Remsima/Remicade by competition assay. Cross-reactivity of anti-adalimumab antibodies with Remicade/Remsima was also investigated.

Results: 125 patients' and controls' sera were tested (median age 31 years, IQR 24.5-39.5). All 56 anti-Remicade ATI-negative controls (14 healthy individuals, 42 patients with IBD) were also negative for anti-Remsima ATI. All 69 positive anti-Remicade IBD sera were cross-reactive with Remsima. ATI titres against Remicade or Remsima were strongly correlated (r values between 0.92 and 0.99, p<0.001 for all experiments, Spearman's correlation test). The background ELISA signal for Remsima was slightly higher compared with Remicade in negative controls (1.25±0.6 µg/mL vs 0.76±0.5 µg/mL, respectively, p<0.001), and persisted after deglycosylation, dialysis or protein size filtration, but abolished by IgG purification and significantly diminished by monomer purification. Anti-Remicade ATIs of patients with IBD (n=10) exerted similar functional inhibition on Remsima or Remicade TNF-α binding capacity (p=NS for all inhibition curve points). Antibodies-to-adalimumab in adalimumab-treated patients with IBD (n=7) did not cross-react with either Remicade or Remsima.

Conclusions: Anti-Remicade antibodies in patients with IBD recognise and functionally inhibit Remsima to a similar degree, suggesting similar immunogenicity and shared immunodominant epitopes on these two infliximab agents. In contrast, anti-adalimumab antibodies do not cross-react with Remsima or Remicade.

Keywords: IBD CLINICAL; IMMUNOTHERAPY.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adalimumab / immunology
  • Adult
  • Aged
  • Antibodies / blood
  • Antibodies / immunology*
  • Antibodies, Monoclonal / chemistry
  • Antibodies, Monoclonal / immunology*
  • Antibodies, Monoclonal / metabolism
  • Biosimilar Pharmaceuticals
  • Cross Reactions
  • Gastrointestinal Agents / immunology*
  • Gastrointestinal Agents / metabolism
  • Glycosylation
  • Humans
  • Immunoglobulin G / immunology
  • Inflammatory Bowel Diseases / drug therapy
  • Infliximab / chemistry
  • Infliximab / immunology*
  • Infliximab / metabolism
  • Middle Aged
  • Tumor Necrosis Factor-alpha / metabolism
  • Young Adult

Substances

  • Antibodies
  • Antibodies, Monoclonal
  • Biosimilar Pharmaceuticals
  • CT-P13
  • Gastrointestinal Agents
  • Immunoglobulin G
  • Tumor Necrosis Factor-alpha
  • Infliximab
  • Adalimumab