Antibodies that neutralize cellular uptake of elosulfase alfa are not associated with reduced efficacy or pharmacodynamic effect in individuals with Morquio A syndrome

J Immunol Methods. 2017 Jan:440:41-51. doi: 10.1016/j.jim.2016.10.006. Epub 2016 Oct 24.

Abstract

Many enzyme replacement therapies (ERTs) for lysosomal storage disorders use the cell-surface cation-independent mannose-6 phosphate receptor (CI-M6PR) to deliver ERTs to the lysosome. However, neutralizing antibodies (NAb) may interfere with this process. We previously reported that most individuals with Morquio A who received elosulfase alfa in the phase 3 MOR-004 trial tested positive for NAbs capable of interfering with binding to CI-M6PR ectodomain in an ELISA-based assay. However, no correlation was detected between NAb occurrence and clinical efficacy or pharmacodynamics. To quantify and better characterize the impact of NAbs, we developed a functional cell-based flow cytometry assay with a titer step that detects antibodies capable of interfering with elosulfase alfa uptake. Serum samples collected during the MOR-004 trial were tested and titers were determined. Consistent with earlier findings on NAb positivity, no correlations were observed between NAb titers and the clinical outcomes of elosulfase alfa-treated individuals with Morquio A.

Keywords: Elosulfase alfa; Enzyme replacement therapy; Lysosomal storage disease; Morquio A; Neutralizing antibody titer.

Publication types

  • Clinical Trial, Phase III
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Neutralizing / blood*
  • Antibodies, Neutralizing / immunology
  • Biological Transport
  • Chondroitinsulfatases / pharmacokinetics
  • Chondroitinsulfatases / therapeutic use*
  • Double-Blind Method
  • Enzyme Replacement Therapy / methods*
  • Flow Cytometry*
  • Humans
  • Jurkat Cells
  • Microscopy, Confocal
  • Mucopolysaccharidosis IV / blood
  • Mucopolysaccharidosis IV / drug therapy*
  • Mucopolysaccharidosis IV / enzymology
  • Mucopolysaccharidosis IV / immunology
  • Receptor, IGF Type 2 / immunology*
  • Receptor, IGF Type 2 / metabolism
  • Serologic Tests / methods*
  • Time Factors
  • Treatment Outcome

Substances

  • Antibodies, Neutralizing
  • Receptor, IGF Type 2
  • cation-dependent mannose-6-phosphate receptor
  • Chondroitinsulfatases
  • GALNS protein, human