Venom Immunotherapy: From Proteins to Product to Patient Protection
Martin Feindor,
Matthew D. Heath,
Simon J. Hewings,
Thalia L. Carreno Velazquez,
Simon Blank,
Johannes Grosch,
Thilo Jakob,
Peter Schmid-Grendelmeier,
Ludger Klimek,
David B. K. Golden,
Murray A. Skinner,
Matthias F. Kramer
Affiliations
Martin Feindor
Allergy Therapeutics (UK) Ltd., Worthing BN14 8SA, UK
Matthew D. Heath
Allergy Therapeutics (UK) Ltd., Worthing BN14 8SA, UK
Simon J. Hewings
Allergy Therapeutics (UK) Ltd., Worthing BN14 8SA, UK
Thalia L. Carreno Velazquez
Allergy Therapeutics (UK) Ltd., Worthing BN14 8SA, UK
Simon Blank
Center of Allergy and Environment (ZAUM), School of Medicine and Helmholtz Center Munich, Technical University of Munich, 85764 Munich, Germany
Johannes Grosch
Center of Allergy and Environment (ZAUM), School of Medicine and Helmholtz Center Munich, Technical University of Munich, 85764 Munich, Germany
Thilo Jakob
Experimental Dermatology and Allergy Research Group, Department of Dermatology and Allergology, University Medical Center Giessen and Marburg, Justus-Liebig-University Gießen, 35390 Giessen, Germany
Peter Schmid-Grendelmeier
Allergy Unit, Department of Dermatology, University Hospital of Zürich, 8091 Zürich, Switzerland
Ludger Klimek
Center for Rhinology and Allergology, 65183 Wiesbaden, Germany
David B. K. Golden
Chesapeake Clinical Research, Baltimore, MA 21236-5992, USA
Murray A. Skinner
Allergy Therapeutics (UK) Ltd., Worthing BN14 8SA, UK
Matthias F. Kramer
Allergy Therapeutics (UK) Ltd., Worthing BN14 8SA, UK
In this review, we outline and reflect on the important differences between allergen-specific immunotherapy for inhalant allergies (i.e., aeroallergens) and venom-specific immunotherapy (VIT), with a special focus on Venomil® Bee and Wasp. Venomil® is provided as a freeze-dried extract and a diluent to prepare a solution for injection for the treatment of patients with IgE-mediated allergies to bee and/or wasp venom and for evaluating the degree of sensitivity in a skin test. While the materials that make up the product have not changed, the suppliers of raw materials have changed over the years. Here, we consolidate relevant historical safety and efficacy studies that used products from shared manufacture supply profiles, i.e., products from Bayer or Hollister–Stier. We also consider the characterization and standardization of venom marker allergens, providing insights into manufacturing controls that have produced stable and consistent quality profiles over many years. Quality differences between products and their impacts on treatment outcomes have been a current topic of discussion and further research. Finally, we review the considerations surrounding the choice of depot adjuvant most suitable to augmenting VIT.