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Development of a hypoallergenic recombinant parvalbumin for first-in-man subcutaneous immunotherapy of fish allergy.

Authors :
Zuidmeer-Jongejan L
Huber H
Swoboda I
Rigby N
Versteeg SA
Jensen BM
Quaak S
Akkerdaas JH
Blom L
Asturias J
Bindslev-Jensen C
Bernardi ML
Clausen M
Ferrara R
Hauer M
Heyse J
Kopp S
Kowalski ML
Lewandowska-Polak A
Linhart B
Maderegger B
Maillere B
Mari A
Martinez A
Mills EN
Neubauer A
Nicoletti C
Papadopoulos NG
Portoles A
Ranta-Panula V
Santos-Magadan S
Schnoor HJ
Sigurdardottir ST
Stahl-Skov P
Stavroulakis G
Stegfellner G
Vázquez-Cortés S
Witten M
Stolz F
Poulsen LK
Fernandez-Rivas M
Valenta R
van Ree R
Source :
International archives of allergy and immunology [Int Arch Allergy Immunol] 2015; Vol. 166 (1), pp. 41-51. Date of Electronic Publication: 2015 Feb 28.
Publication Year :
2015

Abstract

Background: The FAST (food allergy-specific immunotherapy) project aims at developing safe and effective subcutaneous immunotherapy for fish allergy, using recombinant hypoallergenic carp parvalbumin, Cyp c 1.<br />Objectives: Preclinical characterization and good manufacturing practice (GMP) production of mutant Cyp (mCyp) c 1.<br />Methods: Escherichia coli-produced mCyp c 1 was purified using standard chromatographic techniques. Physicochemical properties were investigated by gel electrophoresis, size exclusion chromatography, circular dichroism spectroscopy, reverse-phase high-performance liquid chromatography and mass spectrometry. Allergenicity was assessed by ImmunoCAP inhibition and basophil histamine release assay, immunogenicity by immunization of laboratory animals and stimulation of patients' peripheral blood mononuclear cells (PBMCs). Reference molecules were purified wild-type Cyp c 1 (natural and/or recombinant). GMP-compliant alum-adsorbed mCyp c 1 was tested for acute toxicity in mice and rabbits and for repeated-dose toxicity in mice. Accelerated and real-time protocols were used to evaluate stability of mCyp c 1 as drug substance and drug product.<br />Results: Purified mCyp c 1 behaves as a folded and stable molecule. Using sera of 26 double-blind placebo-controlled food-challenge-proven fish-allergic patients, reduction in allergenic activity ranged from 10- to 5,000-fold (1,000-fold on average), but with retained immunogenicity (immunization in mice/rabbits) and potency to stimulate human PBMCs. Toxicity studies revealed no toxic effects and real-time stability studies on the Al(OH)3-adsorbed drug product demonstrated at least 20 months of stability.<br />Conclusion: The GMP drug product developed for treatment of fish allergy has the characteristics targeted for in FAST: i.e. hypoallergenicity with retained immunogenicity. These results have warranted first-in-man immunotherapy studies to evaluate the safety of this innovative vaccine.<br /> (© 2015 S. Karger AG, Basel.)

Details

Language :
English
ISSN :
1423-0097
Volume :
166
Issue :
1
Database :
MEDLINE
Journal :
International archives of allergy and immunology
Publication Type :
Academic Journal
Accession number :
25765512
Full Text :
https://doi.org/10.1159/000371657