The adsorption of allergoids and 3-O-desacyl-4′-monophosphoryl lipid A (MPL®) to microcrystalline tyrosine (MCT) in formulations for use in allergy immunotherapy

Infectious disease vaccine potency is affected by antigen adjuvant adsorption. WHO and EMA guidelines recommend limits and experimental monitoring of adsorption in vaccines and allergy immunotherapies. Adsorbed allergoids and MPL (R) in MATA-MPL allergy immunotherapy formulations effectively treat IgE mitigated allergy. Understanding vaccine antigen adjuvant adsorption allows optimisation of potency and should be seen as good practice; however current understanding is seldom applied to allergy immunotherapies. The allergoid and MPL (R) adsorption to MCT in MATA-MPL allergy immunotherapy formulations was experimental determination using specific allergen IgE allerginicity and MPL (R) content methods. Binding forces between MPL (R) and MCT were investigated by competition binding experiments. MATA-MPL samples with different allergoids gave results within 100-104% of the theoretical 50 mu g/mL MPL (R) content. Unmodified drug substance samples showed significant desirable IgE antigenicity, 1040-170 QAU/mL MATA-MPL supernatant samples with different allergoids gave results of <= 2 mu g/mL MPL (R) and <= 0.1-1.4 QAU/mL IgE antigenicity, demonstrating approximately >= 96 & 99% adsorption respectively. Allergoid and MPL adsorption in different MATA-MPL allergy immunotherapy formulations is consistent and meets guideline recommendations. MCT formulations treated to disrupt electrostatic, hydrophobic and ligand exchange interactions, gave an MPL content of <= 2 mu g/mL in supernatant samples. MCT formulations treated to disrupt aromatic interactions, gave an MPL (R) content of 73-92 mu g/mL in supematant samples. MPL (R) adsorption to L-tyrosine in MCT formulations is based on interactions between the 2-deoxy-2-aminoglucose backbone on MPL and aromatic ring of L-tyrosine in ma, such as C-H center dot center dot center dot pi interaction. MCT could be an alternative adjuvant depot for some infectious disease antigens. (C) 2015 The Authors. Published by Elsevier Inc.