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Peanut allergy: Beyond the oral immunotherapy plateau

BACKGROUND: There are a lack of disease‐modifying treatments for peanut allergy, which is lifelong in most instances. Oral immunotherapy has remained at the forefront of prospective treatments, though its efficacy is consistently undermined by the risk of adverse reactions and meager sustained effec...

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Autores principales: Bruton, Kelly, Spill, Paul, Chu, Derek K., Waserman, Susan, Jordana, Manel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361810/
https://www.ncbi.nlm.nih.gov/pubmed/34429871
http://dx.doi.org/10.1002/clt2.12046
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author Bruton, Kelly
Spill, Paul
Chu, Derek K.
Waserman, Susan
Jordana, Manel
author_facet Bruton, Kelly
Spill, Paul
Chu, Derek K.
Waserman, Susan
Jordana, Manel
author_sort Bruton, Kelly
collection PubMed
description BACKGROUND: There are a lack of disease‐modifying treatments for peanut allergy, which is lifelong in most instances. Oral immunotherapy has remained at the forefront of prospective treatments, though its efficacy is consistently undermined by the risk of adverse reactions and meager sustained effects. AIM: This review discusses the current state of oral immunotherapy, its strengths and limitations, and the future of therapeutics for the treatment of peanut allergy. CONCLUSION: The persistence of peanut allergy is currently attributed to reservoirs of peanut‐specific memory B cells and Th2 cells, though the cellular and molecular interplay that facilitates the replenishment of peanut‐specific IgE remains elusive. Uncovering these events will prove critical for identification of novel targets as we forge ahead to a new age of peanut allergy treatment with biotherapeutics.
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spelling pubmed-83618102021-08-23 Peanut allergy: Beyond the oral immunotherapy plateau Bruton, Kelly Spill, Paul Chu, Derek K. Waserman, Susan Jordana, Manel Clin Transl Allergy Review BACKGROUND: There are a lack of disease‐modifying treatments for peanut allergy, which is lifelong in most instances. Oral immunotherapy has remained at the forefront of prospective treatments, though its efficacy is consistently undermined by the risk of adverse reactions and meager sustained effects. AIM: This review discusses the current state of oral immunotherapy, its strengths and limitations, and the future of therapeutics for the treatment of peanut allergy. CONCLUSION: The persistence of peanut allergy is currently attributed to reservoirs of peanut‐specific memory B cells and Th2 cells, though the cellular and molecular interplay that facilitates the replenishment of peanut‐specific IgE remains elusive. Uncovering these events will prove critical for identification of novel targets as we forge ahead to a new age of peanut allergy treatment with biotherapeutics. John Wiley and Sons Inc. 2021-08-13 /pmc/articles/PMC8361810/ /pubmed/34429871 http://dx.doi.org/10.1002/clt2.12046 Text en © 2021 The Authors. Clinical and Translational Allergy published by John Wiley and 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 Review
Bruton, Kelly
Spill, Paul
Chu, Derek K.
Waserman, Susan
Jordana, Manel
Peanut allergy: Beyond the oral immunotherapy plateau
title Peanut allergy: Beyond the oral immunotherapy plateau
title_full Peanut allergy: Beyond the oral immunotherapy plateau
title_fullStr Peanut allergy: Beyond the oral immunotherapy plateau
title_full_unstemmed Peanut allergy: Beyond the oral immunotherapy plateau
title_short Peanut allergy: Beyond the oral immunotherapy plateau
title_sort peanut allergy: beyond the oral immunotherapy plateau
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361810/
https://www.ncbi.nlm.nih.gov/pubmed/34429871
http://dx.doi.org/10.1002/clt2.12046
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