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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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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 |
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author | 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 |
author_facet | 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 |
author_sort | Albanesi, Marcello |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5774115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57741152018-01-26 A 13-year real-life study on efficacy, safety and biological effects of Vespula venom immunotherapy 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 Clin Mol Allergy Research 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. BioMed Central 2018-01-18 /pmc/articles/PMC5774115/ /pubmed/29375272 http://dx.doi.org/10.1186/s12948-017-0079-y Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research 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 A 13-year real-life study on efficacy, safety and biological effects of Vespula venom immunotherapy |
title | A 13-year real-life study on efficacy, safety and biological effects of Vespula venom immunotherapy |
title_full | A 13-year real-life study on efficacy, safety and biological effects of Vespula venom immunotherapy |
title_fullStr | A 13-year real-life study on efficacy, safety and biological effects of Vespula venom immunotherapy |
title_full_unstemmed | A 13-year real-life study on efficacy, safety and biological effects of Vespula venom immunotherapy |
title_short | A 13-year real-life study on efficacy, safety and biological effects of Vespula venom immunotherapy |
title_sort | 13-year real-life study on efficacy, safety and biological effects of vespula venom immunotherapy |
topic | Research |
url | 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 |
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