The next generation virus‐like particle platform for the treatment of peanut allergy

Author:

Sobczak Jan M.12ORCID,Krenger Pascal S.12,Storni Federico123ORCID,Mohsen Mona O.12,Balke Ina4ORCID,Reseviča Gunta4,Heath Matthew D.5ORCID,Carreno Velazquez Thalia L.5,Kramer Matthias F.6ORCID,Scott Callum J. W.5,Skinner Murray A.5,Zeltiņš Andris4,Kündig Thomas M.7,Vogel Monique12ORCID,Bachmann Martin F.128ORCID

Affiliation:

1. Department of Immunology University Clinic of Rheumatology and Immunology, Inselspital Bern Switzerland

2. Department of BioMedical Research University of Bern Bern Switzerland

3. Department of Visceral Surgery and Medicine Inselspital, University Hospital Bern Bern Switzerland

4. Latvian Biomedical Research and Study Centre Riga Latvia

5. Allergy Therapeutics (UK) Ltd. Worthing UK

6. Bencard Allergie GmbH Munich Germany

7. Department of Dermatology University Hospital Zurich, University of Zurich Zurich Switzerland

8. Nuffield Department of Medicine The Jenner Institute, University of Oxford Oxford UK

Abstract

AbstractBackgroundAllergy to peanut is one of the leading causes of anaphylactic reactions among food allergic patients. Immunization against peanut allergy with a safe and protective vaccine holds a promise to induce durable protection against anaphylaxis caused by exposure to peanut. A novel vaccine candidate (VLP Peanut), based on virus‐like particles (VLPs), is described here for the treatment of peanut allergy.Methods and ResultsVLP Peanut consists of two proteins: a capsid subunit derived from Cucumber mosaic virus engineered with a universal T‐cell epitope (CuMVTT) and a CuMVTT subunit fused with peanut allergen Ara h 2 (CuMVTT‐Ara h 2), forming mosaic VLPs. Immunizations with VLP Peanut in both naïve and peanut‐sensitized mice resulted in a significant anti‐Ara h 2 IgG response. Local and systemic protection induced by VLP Peanut were established in mouse models for peanut allergy following prophylactic, therapeutic, and passive immunizations. Inhibition of FcγRIIb function resulted in a loss of protection, confirming the crucial role of the receptor in conferring cross protection against peanut allergens other than Ara h 2.ConclusionVLP Peanut can be delivered to peanut‐sensitized mice without triggering allergic reactions, while remaining highly immunogenic and offering protection against all peanut allergens. In addition, vaccination ablates allergic symptoms upon allergen challenge. Moreover, the prophylactic immunization setting conferred the protection against subsequent peanut‐induced anaphylaxis, showing the potential for preventive vaccination. This highlights the effectiveness of VLP Peanut as a prospective break‐through immunotherapy vaccine candidate toward peanut allergy. VLP Peanut has now entered clinical development with the study PROTECT.

Funder

Allergy Therapeutics

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

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