Modulation of allergic responses in mice by using biodegradable poly(lactide- co-glycolide) microspheres

• Published in: Journal of allergy and clinical immunology 2004-10, Vol.114 (4), p.943-950
• Main Authors: Jilek, Samantha, Walter, Elke, Merkle, Hans P., Corthésy, Blaise
• Format: Article
• Language: English
• Subjects: Absorbable Implants; Allergies; Allergy; Animals; Bee Venoms - immunology; Biocompatible Materials - administration & dosage; Biological and medical sciences; Cell growth; Deoxyribonucleic acid; DNA; Drug Carriers; Fundamental and applied biological sciences. Psychology; Fundamental immunology; Hypersensitivity - immunology; Hypersensitivity - therapy; Immunization; immunomodulation; Immunopathology; Injections, Subcutaneous; Interleukin-10 - immunology; Medical sciences; Mice; Microspheres; Models, Animal; Molecular weight; Phospholipases A - immunology; Phospholipases A2; Polyglactin 910 - administration & dosage; Production increases; T H1/T H2 responses; T-Lymphocytes - immunology; Vaccination - instrumentation; Vaccines, DNA - administration & dosage
• ISSN: 0091-6749; 1097-6825
• DOI: 10.1016/j.jaci.2004.05.065

Biodegradable poly(lactide- co-glycolide) (PLGA) microspheres are a promising carrier for vaccine delivery capable of maturing antigen-presenting cells to stimulate T-cell–mediated immune responses. However, the potential of microspheres to downregulate an allergic response in vivo is unknown. The aim of this study was to determine whether microspheres could potentiate DNA vaccination against allergy and to evaluate the immunomodulatory properties of microspheres alone. Mice were treated prophylactically with DNA-loaded plain PLGA microspheres before sensitization with phospholipase A2 (PLA2), the major allergen of bee venom. PLA2-specific IgG1, IgG2a, IgE in serum were measured for 8.5 months, and splenocyte proliferative responses and cytokine profiles were determined. Protection against anaphylaxis was evaluated after injection of an otherwise lethal dose of PLA2. Phospholipase A2–specific IgG1 and IgG2a production turned out to be 2 times higher using cationic microspheres compared with anionic microspheres, but was not influenced by the presence of DNA. In contrast, reduction in IgE production and T-cell hyporesponsiveness were observed with all microsphere formulations. Recall challenge with PLA2 triggered combined expression of both IL-4 and IFN-γ, together with sustained expression of IL-10 that can explain the protective effect against anaphylaxis. Our data suggest a dual mechanism that does initially rely on a T H2 to T H1 immune deviation and then on IL-10-mediated suppression. This is the first physiological demonstration that plain PLGA microspheres can induce tolerance in mice for as long as 6 months postsensitization.