4.5 Article

Analytical characterization of ch14.18 A mouse-human chimeric disialoganglioside-specific therapeutic antibody

Journal

MABS
Volume 4, Issue 1, Pages 84-100

Publisher

TAYLOR & FRANCIS INC
DOI: 10.4161/mabs.4.1.18566

Keywords

monoclonal antibodies; chimeric antibody; characterization assays; SEC-MALS; imaged cIEF; N-glycoprofiling; N-glycan analysis; Fc gamma RIIIA:ch14.18 interaction; surface plasmon resonance; complement-dependent cytotoxicity

Funding

  1. National Cancer Institute, National Institutes of Health [HHSN261200800001E]
  2. Division of Cancer Treatment and Diagnosis of the National Cancer Institute
  3. Biological Resources Branch of NCI

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Ch14.18 is a mouse-human chimeric monoclonal antibody to the disialoganglioside (GD2) glycolipid. In the clinic, this antibody has been shown to be effective in the treatment of children with high-risk neuroblastoma, either alone or in combination therapy. Extensive product characterization is a prerequisite to addressing the potential issues of product variability associated with process changes and manufacturing scale-up. Charge heterogeneity, glycosylation profile, molecular state and aggregation, interaction (affinity) with Fc gamma receptors and functional or biological activities are a few of the critical characterization assays for assessing product comparability for this antibody. In this article, we describe the in-house development and qualification of imaged capillary isoelectric focusing to assess charge heterogeneity, analytical size exclusion chromatography with online static and dynamic light scattering (DLS), batch mode DLS for aggregate detection, biosensor (surface plasmon resonance)-based Fc gamma receptor antibody interaction kinetics, N-glycoprofiling with PNGase F digestion, 2-aminobenzoic acid labeling and high performance liquid chromatography and N-glycan analysis using capillary electrophoresis. In addition, we studied selected biological activity assays, such as complement-dependent cytotoxicity. The consistency and reproducibility of the assays are established by comparing the intra-day and inter-day assay results. Applications of the methodologies to address stability or changes in product characteristics are also reported. The study results reveal that the ch14.18 clinical product formulated in phosphate-buffered saline at a concentration of 5 mg/ml and stored at 2-8 degrees C is stable for more than five years.

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