Pharmaceutical and preclinical evaluation of Advax adjuvant as a dose-sparing strategy for ant venom immunotherapy.
Adjuvants, Immunologic
/ administration & dosage
Allergens
/ administration & dosage
Animals
Ant Venoms
/ administration & dosage
Desensitization, Immunologic
/ methods
Dose-Response Relationship, Drug
Drug Evaluation, Preclinical
Drug Stability
Female
Humans
Hypersensitivity
/ immunology
Inulin
/ administration & dosage
Mice
Models, Animal
Adjuvants
Advax
Allergy
Delta inulin
Venom immunotherapy
Journal
Journal of pharmaceutical and biomedical analysis
ISSN: 1873-264X
Titre abrégé: J Pharm Biomed Anal
Pays: England
ID NLM: 8309336
Informations de publication
Date de publication:
05 Aug 2019
05 Aug 2019
Historique:
received:
08
10
2018
revised:
07
04
2019
accepted:
08
04
2019
pubmed:
23
4
2019
medline:
30
11
2019
entrez:
23
4
2019
Statut:
ppublish
Résumé
A major challenge in broader clinical application of Jack Jumper ant venom immunotherapy (JJA VIT) is the scarcity of ant venom which needs to be manually harvested from wild ants. Adjuvants are commonly used for antigen sparing in other vaccines, and thereby could potentially have major benefits to extend JJA supplies if they were to similarly enhance JJA VIT immunogenicity. The purpose of this study was to evaluate the physicochemical and microbiological stability and murine immunogenicity of low-dose JJA VIT formulated with a novel polysaccharide adjuvant referred to as delta inulin or Advax™. Jack Jumper ant venom (JJAV) protein stability was assessed by UPLC-UV, SDS-PAGE, SDS-PAGE immunoblot, and ELISA inhibition. Diffraction light scattering was used to assess particle size distribution of Advax; pH and benzyl alcohol quantification by UPLC-UV were used to assess the physicochemical stability of JJAV diluent, and endotoxin content and preservative efficacy test was used to investigate the microbiological properties of the adjuvanted VIT formulation. To assess the effect of adjuvant on JJA venom immunogenicity, mice were immunised four times with JJAV alone or formulated with Advax adjuvant. JJA VIT formulated with Advax was found to be physicochemically and microbiologically stable for at least 2 days when stored at 4 and 25 °C with a trend for an increase in allergenic potency observed beyond 2 days of storage. Low-dose JJAV formulated with Advax adjuvant induced significantly higher JJAV-specific IgG than a 5-fold higher dose of JJAV alone, consistent with a powerful allergen-sparing effect. The pharmaceutical data provides important guidance on the formulation, storage and use of JJA VIT formulated with Advax adjuvant, with the murine immunogenicity studies providing a strong rationale for a planned clinical trial to test the ability of Advax adjuvant to achieve 4-fold JJAV dose sparing in JJA-allergic human patients.
Identifiants
pubmed: 31009889
pii: S0731-7085(18)32278-7
doi: 10.1016/j.jpba.2019.04.017
pmc: PMC7127811
pii:
doi:
Substances chimiques
Adjuvants, Immunologic
0
Allergens
0
Ant Venoms
0
delta inulin
0
Inulin
9005-80-5
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1-8Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.
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