Multivalent paediatric allergy vaccines protect against allergic anaphylaxis in mice

• Published in: Clinical and experimental allergy 2014-03, Vol.44 (3), p.429-437
• Main Authors: Waeckerle-Men, Y., Liang, Y., von Moos, S., Kündig, T. M., Johansen, P.
• Format: Article
• Language: English
• Subjects: Adoptive Transfer; Allergens - immunology; anaphylaxis; Anaphylaxis - immunology; Anaphylaxis - prevention & control; Animals; antibodies; childhood vaccine; Cross Protection - immunology; Disease Models, Animal; Female; Humans; Immunization Schedule; Immunoglobulin E - blood; Immunoglobulin E - immunology; Immunoglobulin G - blood; Immunoglobulin G - immunology; Mice; murine model of allergy; Ovalbumin - adverse effects; Rhinitis, Allergic; Rhinitis, Allergic, Perennial - prevention & control; T cells; Vaccines - immunology
• ISSN: 0954-7894; 1365-2222
• DOI: 10.1111/cea.12245

Summary Background Almost a quarter of the world population suffers from IgE‐mediated allergies. T cells and IgG‐producing B cells can produce protection, but treatment for disease is laborious with unsatisfactory patient compliance. Objective We sought to identify whether paediatric allergy vaccines affected later allergen sensitization and onset of disease when used prophylactically. Methods A murine model of anaphylaxis was applied. Mice were first immunized with monovalent or multivalent allergy vaccines that also contained aluminium hydroxide and CpG oligodeoxynucleotide as adjuvants. Later, the mice were sensitized by multiple low‐dose injections of aluminium‐adsorbed allergen. After a dormant period, the mice were challenged systemically with high‐dose allergen, and the clinical signs of anaphylaxis were recorded. Throughout the immunization and sensitization periods, blood was collected for serological testing. Results Immunization with allergy vaccines produced antigen‐specific protection against sensitization as measured by systemic anaphylaxis in mice. The long‐term effect was observed both after juvenile (5–6 weeks) and neonatal (7 days) vaccination. Monovalent and pentavalent vaccines were protective to a similar level. Protection was associated with increased secretion of IgG2a and production of IFN‐γ. Protection could also be transferred to sensitized mice via serum or via CD25‐positive CD4 T cells. Conclusion and clinical relevance Prophylactic and multivalent allergy vaccines in juvenile and neonatal mice protected against later sensitization and anaphylaxis. Such treatment may provide a rational measure for future management of allergen‐related diseases and their strong socio‐economic impact on daily life.