TY - JOUR
T1 - Production of allergen-specific immunotherapeutic agents for the treatment of food allergy
AU - Larsen, Jeppe Madura
AU - Bang-Berthelsen, Claus Heiner
AU - Qvortrup, Katrine
AU - Sancho, Ana Isabel
AU - Hansen, Anders Højgaard
AU - Andersen, Kasper Ivert Hentzer
AU - Thacker, Sonnich Sunil Nørtoft
AU - Eiwegger, Thomas
AU - Upton, Julia
AU - Bøgh, Katrine Lindholm
N1 - Publisher Copyright:
© 2020, © 2020 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2020/8/17
Y1 - 2020/8/17
N2 - Allergen-specific immunotherapy (IT) is emerging as a viable avenue for the treatment of food allergies. Clinical trials currently investigate raw or slightly processed foods as therapeutic agents, as trials using food-grade agents can be performed without the strict regulations to which conventional drugs are subjected. However, this limits the ability of standardization and may affect clinical trial outcomes and reproducibility. Herein, we provide an overview of methods used in the production of immunotherapeutic agents for the treatment of food allergies, including processed foods, allergen extracts, recombinant allergens, and synthetic peptides, as well as the physical and chemical processes for the reduction of protein allergenicity. Commercial interests currently favor producing standardized drug-grade allergen extracts for therapeutic use, and clinical trials are ongoing. In the near future, recombinant production could replace purification strategies since it allows the manufacturing of pure, native allergens or sequence-modified allergens with reduced allergenicity. A recurring issue within this field is the inadequate reporting of production procedures, quality control, product physicochemical characteristics, allergenicity, and immunological properties. This information is of vital importance in assessing therapeutic standardization and clinical safety profile, which are central parameters for the development of future therapeutic agents.
AB - Allergen-specific immunotherapy (IT) is emerging as a viable avenue for the treatment of food allergies. Clinical trials currently investigate raw or slightly processed foods as therapeutic agents, as trials using food-grade agents can be performed without the strict regulations to which conventional drugs are subjected. However, this limits the ability of standardization and may affect clinical trial outcomes and reproducibility. Herein, we provide an overview of methods used in the production of immunotherapeutic agents for the treatment of food allergies, including processed foods, allergen extracts, recombinant allergens, and synthetic peptides, as well as the physical and chemical processes for the reduction of protein allergenicity. Commercial interests currently favor producing standardized drug-grade allergen extracts for therapeutic use, and clinical trials are ongoing. In the near future, recombinant production could replace purification strategies since it allows the manufacturing of pure, native allergens or sequence-modified allergens with reduced allergenicity. A recurring issue within this field is the inadequate reporting of production procedures, quality control, product physicochemical characteristics, allergenicity, and immunological properties. This information is of vital importance in assessing therapeutic standardization and clinical safety profile, which are central parameters for the development of future therapeutic agents.
KW - Allergens/immunology
KW - Animals
KW - Desensitization, Immunologic
KW - Food Handling
KW - Food Hypersensitivity/drug therapy
KW - Humans
KW - Peptides/immunology
KW - Recombinant Proteins/immunology
UR - http://www.scopus.com/inward/record.url?scp=85086852810&partnerID=8YFLogxK
U2 - 10.1080/07388551.2020.1772194
DO - 10.1080/07388551.2020.1772194
M3 - Review article
C2 - 32515236
SN - 0738-8551
VL - 40
SP - 881
EP - 894
JO - Critical Reviews in Biotechnology
JF - Critical Reviews in Biotechnology
IS - 6
ER -