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Generation of a virus-like particles based vaccine against IgE.
Gharailoo, Zahra; Plattner, Kevin; Augusto, Gilles; Engeroff, Paul; Vogel, Monique; Bachmann, Martin F.
Afiliación
  • Gharailoo Z; Department of Immunology, University Clinic for Rheumatology and Immunology, University of Bern, Bern, Switzerland.
  • Plattner K; Department of Biomedical Research Bern (DBMR), University of Bern, Bern, Switzerland.
  • Augusto G; Graduate School for Cellular and Biomedical Sciences (GCB), Bern, Switzerland.
  • Engeroff P; Department of Immunology, University Clinic for Rheumatology and Immunology, University of Bern, Bern, Switzerland.
  • Vogel M; Department of Biomedical Research Bern (DBMR), University of Bern, Bern, Switzerland.
  • Bachmann MF; Graduate School for Cellular and Biomedical Sciences (GCB), Bern, Switzerland.
Allergy ; 79(8): 2207-2221, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38445568
ABSTRACT

BACKGROUND:

Anti-IgE immunotherapy with monoclonal antibodies represents a breakthrough in treatment of severe allergic diseases. However, drawbacks such as short half-life and high price are not negligible. Our objective is to develop an anti-IgE vaccine based on virus-like particles (VLPs) which can induce long-lasting neutralizing IgG anti-IgE antibodies reducing allergic responses without causing intrinsic mast cell activation due to IgE cross-linking.

METHODS:

The vaccines were made by chemically coupling three synthetic mouse IgE-Fc fragments to plant-derived immunologically optimized CuMVTT VLPs. The immunogenicity of the vaccines was tested by immunizing naive or allergic mice either with the coupled vaccines or the VLP control followed by systemic or local allergen challenge.

RESULTS:

Mice immunized with the vaccines exhibited high titers of anti-IgE antibodies in the sera and high levels of anti-IgE secreting plasma cells in lymphoid organs. Moreover, free IgE in serum were reduced by the induced anti-IgE antibodies; therefore, less IgE was bound to FcεRI on the surface of basophils. In line with these reduced IgE levels on effector cells after vaccination, immunized mice were protected from challenge with allergens. Importantly, despite presence of anti-IgE antibodies, no signs of acute or chronic allergic response were seen in immunized allergic mice.

CONCLUSION:

The generated vaccines can effectively induce anti-IgE antibodies that did not cause allergic responses in sensitized mice but were able to decrease the level of free and cell bound IgE and protected sensitized animals from allergic responses upon allergen challenge.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inmunoglobulina E / Vacunas de Partículas Similares a Virus Límite: Animals Idioma: En Revista: Allergy Año: 2024 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Dinamarca
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inmunoglobulina E / Vacunas de Partículas Similares a Virus Límite: Animals Idioma: En Revista: Allergy Año: 2024 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Dinamarca