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A 13-year real-life study on efficacy, safety and biological effects of Vespula venom immunotherapy

BACKGROUND: Hymenoptera venom immunotherapy (VIT) is a clinically effective treatment. However, little is known about its long-term clinical efficacy and biological effects. Several mechanisms have been proposed to account for VIT efficacy, including reduction of specific IgE and induction of allerg...

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Detalles Bibliográficos
Autores principales: Albanesi, Marcello, Nico, Andrea, Sinisi, Alessandro, Giliberti, Lucia, Rossi, Maria Pia, Rossini, Margherita, Kourtis, Georgios, Rucco, Anna Simona, Loconte, Filomena, Muolo, Loredana, Zurlo, Marco, Di Bona, Danilo, Caiaffa, Maria Filomena, Macchia, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5774115/
https://www.ncbi.nlm.nih.gov/pubmed/29375272
http://dx.doi.org/10.1186/s12948-017-0079-y
Descripción
Sumario:BACKGROUND: Hymenoptera venom immunotherapy (VIT) is a clinically effective treatment. However, little is known about its long-term clinical efficacy and biological effects. Several mechanisms have been proposed to account for VIT efficacy, including reduction of specific IgE and induction of allergen-specific IgG(4), but the overall picture remains elusive. We investigated Vespula VIT clinical efficacy up to 8 years after discontinuation and the kinetics of Vespula-specific IgE and IgG(4). Out of 686 consecutive patients we retrospectively selected and analysed a series of 23 patients with Vespula allergy that underwent a 5-year IT course, followed by a prolonged follow-up. METHODS: Clinical efficacy of VIT was assessed as number and severity of reactions to Vespula re-stinging events. The presence of Vespula-specific IgE and IgG(4) was also monitored over time. RESULTS: During the VIT treatment, patients were protected, reporting no reactions or mild reactions in occasion of re-stinging events. This protection was entirely maintained during the follow-up, up to 8 years. Skin reactivity (reflecting mast cell-bound Vespula-specific IgE) and circulating Vespula-specific IgE levels declined substantially during VIT. Notably, this reduction was maintained over time during the follow-up. Moreover, all the patients were analysed for IgG(4). A robust induction of Vespula-specific IgG(4) was observed during the VIT course, with a substantial decline during the follow-up. CONCLUSIONS: We conclude that Vespula VIT is a clinically effective treatment, which induces long-term protection after discontinuation. The reduction of specific IgE, assessed by skin tests and RAST, closely matches the VIT- induced protection, while the IgG(4) induction seems not to be associated with VIT clinical efficacy in the long term. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12948-017-0079-y) contains supplementary material, which is available to authorized users.