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Systematic review of monotherapy with biologicals for children and adults with IgE‐mediated food allergy

BACKGROUND: Biological therapies relieve symptoms in allergic inflammatory diseases so we systematically reviewed the evidence about whether biological monotherapy could benefit people with IgE‐mediated food allergy. METHODS: We searched six bibliographic databases from 1946 to 30 September 2021 for...

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Autores principales: de Silva, Debra, Singh, Chris, Arasi, Stefania, Muraro, Antonella, Zuberbier, Torsten, Ebisawa, Motohiro, Alvaro Lozano, Montserrat, Roberts, Graham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515515/
https://www.ncbi.nlm.nih.gov/pubmed/36204600
http://dx.doi.org/10.1002/clt2.12123
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author de Silva, Debra
Singh, Chris
Arasi, Stefania
Muraro, Antonella
Zuberbier, Torsten
Ebisawa, Motohiro
Alvaro Lozano, Montserrat
Roberts, Graham
author_facet de Silva, Debra
Singh, Chris
Arasi, Stefania
Muraro, Antonella
Zuberbier, Torsten
Ebisawa, Motohiro
Alvaro Lozano, Montserrat
Roberts, Graham
author_sort de Silva, Debra
collection PubMed
description BACKGROUND: Biological therapies relieve symptoms in allergic inflammatory diseases so we systematically reviewed the evidence about whether biological monotherapy could benefit people with IgE‐mediated food allergy. METHODS: We searched six bibliographic databases from 1946 to 30 September 2021 for randomised and non‐randomised controlled trials about biological monotherapy in people with IgE‐mediated food allergy confirmed by oral food challenge. We used the Grading of Recommendations, Assessment, Development and Evaluation approach to narratively summarise findings from three trials with 118 participants. The studies were too heterogeneous and sparse to conduct meta‐analysis. RESULTS: We included one randomised trial about etokimab, one about omalizumab and one about the discontinued TNX‐901. All were in people with peanut allergy in the USA, mostly aged 13+ years. There was a trend towards improved tolerance of peanut during treatment, with few side effects. However, we have very low certainty about the evidence due to the small number of trials and participants. No included trial reported on quality of life or cost‐effectiveness. CONCLUSIONS: There is not yet enough certainty to support offering etokimab or omalizumab widely for food allergy. Clinicians may consider the merits for individuals, but large randomised trials with standardised measures are needed to confirm the safety, efficacy and most suitable candidates, doses and durations of treatment before more universal use.
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spelling pubmed-95155152022-10-05 Systematic review of monotherapy with biologicals for children and adults with IgE‐mediated food allergy de Silva, Debra Singh, Chris Arasi, Stefania Muraro, Antonella Zuberbier, Torsten Ebisawa, Motohiro Alvaro Lozano, Montserrat Roberts, Graham Clin Transl Allergy Original Article BACKGROUND: Biological therapies relieve symptoms in allergic inflammatory diseases so we systematically reviewed the evidence about whether biological monotherapy could benefit people with IgE‐mediated food allergy. METHODS: We searched six bibliographic databases from 1946 to 30 September 2021 for randomised and non‐randomised controlled trials about biological monotherapy in people with IgE‐mediated food allergy confirmed by oral food challenge. We used the Grading of Recommendations, Assessment, Development and Evaluation approach to narratively summarise findings from three trials with 118 participants. The studies were too heterogeneous and sparse to conduct meta‐analysis. RESULTS: We included one randomised trial about etokimab, one about omalizumab and one about the discontinued TNX‐901. All were in people with peanut allergy in the USA, mostly aged 13+ years. There was a trend towards improved tolerance of peanut during treatment, with few side effects. However, we have very low certainty about the evidence due to the small number of trials and participants. No included trial reported on quality of life or cost‐effectiveness. CONCLUSIONS: There is not yet enough certainty to support offering etokimab or omalizumab widely for food allergy. Clinicians may consider the merits for individuals, but large randomised trials with standardised measures are needed to confirm the safety, efficacy and most suitable candidates, doses and durations of treatment before more universal use. John Wiley and Sons Inc. 2022-09-27 /pmc/articles/PMC9515515/ /pubmed/36204600 http://dx.doi.org/10.1002/clt2.12123 Text en © 2022 The Authors. Clinical and Translational Allergy published by John Wiley & Sons Ltd on behalf of European Academy of Allergy and Clinical Immunology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
de Silva, Debra
Singh, Chris
Arasi, Stefania
Muraro, Antonella
Zuberbier, Torsten
Ebisawa, Motohiro
Alvaro Lozano, Montserrat
Roberts, Graham
Systematic review of monotherapy with biologicals for children and adults with IgE‐mediated food allergy
title Systematic review of monotherapy with biologicals for children and adults with IgE‐mediated food allergy
title_full Systematic review of monotherapy with biologicals for children and adults with IgE‐mediated food allergy
title_fullStr Systematic review of monotherapy with biologicals for children and adults with IgE‐mediated food allergy
title_full_unstemmed Systematic review of monotherapy with biologicals for children and adults with IgE‐mediated food allergy
title_short Systematic review of monotherapy with biologicals for children and adults with IgE‐mediated food allergy
title_sort systematic review of monotherapy with biologicals for children and adults with ige‐mediated food allergy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515515/
https://www.ncbi.nlm.nih.gov/pubmed/36204600
http://dx.doi.org/10.1002/clt2.12123
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