Clinical and Translational Allergy (Mar 2012)

FAST: towards safe and effective subcutaneous immunotherapy of persistent life-threatening food allergies

  • Zuidmeer-Jongejan Laurian,
  • Fernandez-Rivas Montserrat,
  • Poulsen Lars K,
  • Neubauer Angela,
  • Asturias Juan,
  • Blom Lars,
  • Boye Joyce,
  • Bindslev-Jensen Carsten,
  • Clausen Michael,
  • Ferrara Rosa,
  • Garosi Paula,
  • Huber Hans,
  • Jensen Bettina M,
  • Koppelman Stef,
  • Kowalski Marek L,
  • Lewandowska-Polak Anna,
  • Linhart Birgit,
  • Maillere Bernard,
  • Mari Adriano,
  • Martinez Alberto,
  • Mills Clare EN,
  • Nicoletti Claudio,
  • Opstelten Dirk-Jan,
  • Papadopoulos Nikos G,
  • Portoles Antonio,
  • Rigby Neil,
  • Scala Enrico,
  • Schnoor Heidi J,
  • Sigurdardottir Sigurveig T,
  • Stavroulakis George,
  • Stolz Frank,
  • Swoboda Ines,
  • Valenta Rudolf,
  • van den Hout Rob,
  • Versteeg Serge A,
  • Witten Marianne,
  • van Ree Ronald

DOI
https://doi.org/10.1186/2045-7022-2-5
Journal volume & issue
Vol. 2, no. 1
p. 5

Abstract

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Abstract The FAST project (Food Allergy Specific Immunotherapy) aims at the development of safe and effective treatment of food allergies, targeting prevalent, persistent and severe allergy to fish and peach. Classical allergen-specific immunotherapy (SIT), using subcutaneous injections with aqueous food extracts may be effective but has proven to be accompanied by too many anaphylactic side-effects. FAST aims to develop a safe alternative by replacing food extracts with hypoallergenic recombinant major allergens as the active ingredients of SIT. Both severe fish and peach allergy are caused by a single major allergen, parvalbumin (Cyp c 1) and lipid transfer protein (Pru p 3), respectively. Two approaches are being evaluated for achieving hypoallergenicity, i.e. site-directed mutagenesis and chemical modification. The most promising hypoallergens will be produced under GMP conditions. After pre-clinical testing (toxicology testing and efficacy in mouse models), SCIT with alum-absorbed hypoallergens will be evaluated in phase I/IIa and IIb randomized double-blind placebo-controlled (DBPC) clinical trials, with the DBPC food challenge as primary read-out. To understand the underlying immune mechanisms in depth serological and cellular immune analyses will be performed, allowing identification of novel biomarkers for monitoring treatment efficacy. FAST aims at improving the quality of life of food allergic patients by providing a safe and effective treatment that will significantly lower their threshold for fish or peach intake, thereby decreasing their anxiety and dependence on rescue medication.

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