Federico Storni1,2,3, Gustavo Cabral-Miranda4,5, Elisa Roesti4,5, Lisha Zha6, Paul Engeroff4,5, Andris Zeltins7, Mark Cragg8, Monique Vogel4,5, Martin F Bachmann4,5,9. 1. Immunology, RIA, Inselspital, University of Bern, Bern, Switzerland, federico.storni@insel.ch. 2. Department of BioMedical Research, University of Bern, Bern, Switzerland, federico.storni@insel.ch. 3. Department of Visceral Surgery and Medicine, University Hospital of Bern, Bern, Switzerland, federico.storni@insel.ch. 4. Immunology, RIA, Inselspital, University of Bern, Bern, Switzerland. 5. Department of BioMedical Research, University of Bern, Bern, Switzerland. 6. International Immunology Center of Anhui Agricultural Center, Anhui, China. 7. Latvian Biomedical Research and Study Centre (BRSC), Riga, Latvia. 8. Antibody and Vaccine Group, Centre for Cancer Immunology, Cancer Sciences Unit, Faculty of Medicine, General Hospital, University of Southampton, Southampton, United Kingdom. 9. Nuffield Department of Medicine, Centre for Cellular and Molecular Physiology (CCMP), The Jenner Institute, University of Oxford, Oxford, United Kingdom.
Abstract
BACKGROUND: Peanut allergy is the most prevalent and dangerous food allergy. Peanuts consist of a large number of different allergens and peanut-allergic patients are frequently sensitized to multiple allergens. Hence, conventional desensitization approaches aim at targeting as many allergens as possible. METHODS: The monoclonal anti-Ara h 2 antibody (mAb) was produced by hybridoma cells derived from WT BALB/c mice after immunization with a vaccine based on virus-like particles coupled to Ara h 2. BALB/c mice were sensitized intraperitoneally with peanut extract absorbed to alum and mAbs were applied i.v. Challenge was performed the next day with the whole peanut extract intravenously and via skin prick test. RESULTS: Here we show in peanut-allergic mice that a single high-affinity mAb specific for Ara h 2 is able to block systemic and local allergic reactions induced by the complex peanut extract. We confirm in vitro binding of the mAb to the inhibitory low-affinity FcγRIIb receptor using a sensitive biosensor and demonstrate in vivo that protection was dependent on FcγRIIb. CONCLUSION: A single mAb specific for Ara h 2 is able to improve local and systemic allergic symptoms induced by the whole allergen mixture.
BACKGROUND:Peanutallergy is the most prevalent and dangerous food allergy. Peanuts consist of a large number of different allergens and peanut-allergicpatients are frequently sensitized to multiple allergens. Hence, conventional desensitization approaches aim at targeting as many allergens as possible. METHODS: The monoclonal anti-Ara h 2 antibody (mAb) was produced by hybridoma cells derived from WT BALB/c mice after immunization with a vaccine based on virus-like particles coupled to Ara h 2. BALB/c mice were sensitized intraperitoneally with peanut extract absorbed to alum and mAbs were applied i.v. Challenge was performed the next day with the whole peanut extract intravenously and via skin prick test. RESULTS: Here we show in peanut-allergicmice that a single high-affinity mAb specific for Ara h 2 is able to block systemic and local allergic reactions induced by the complex peanut extract. We confirm in vitro binding of the mAb to the inhibitory low-affinity FcγRIIb receptor using a sensitive biosensor and demonstrate in vivo that protection was dependent on FcγRIIb. CONCLUSION: A single mAb specific for Ara h 2 is able to improve local and systemic allergic symptoms induced by the whole allergen mixture.
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