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Aggregation of protein therapeutics enhances their immunogenicity: causes and mitigation strategies

Protein aggregation in biotherapeutics has been identified to increase immunogenicity, leading to immune-mediated adverse effects, such as severe allergic responses including anaphylaxis. The induction of anti-drug antibodies (ADAs) moreover enhances drug clearance rates, and can directly block ther...

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Autores principales: Lundahl, Mimmi L. E., Fogli, Silvia, Colavita, Paula E., Scanlan, Eoin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8341748/
https://www.ncbi.nlm.nih.gov/pubmed/34458822
http://dx.doi.org/10.1039/d1cb00067e
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author Lundahl, Mimmi L. E.
Fogli, Silvia
Colavita, Paula E.
Scanlan, Eoin M.
author_facet Lundahl, Mimmi L. E.
Fogli, Silvia
Colavita, Paula E.
Scanlan, Eoin M.
author_sort Lundahl, Mimmi L. E.
collection PubMed
description Protein aggregation in biotherapeutics has been identified to increase immunogenicity, leading to immune-mediated adverse effects, such as severe allergic responses including anaphylaxis. The induction of anti-drug antibodies (ADAs) moreover enhances drug clearance rates, and can directly block therapeutic function. In this review, identified immune activation mechanisms triggered by protein aggregates are discussed, as well as physicochemical properties of aggregates, such as size and shape, which contribute to immunogenicity. Furthermore, factors which contribute to protein stability and aggregation are considered. Lastly, with these factors in mind, we encourage an innovative and multidisciplinary approach with regard to further research in the field, with the overall aim to avoid immunogenic aggregation in future drug development.
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spelling pubmed-83417482021-08-26 Aggregation of protein therapeutics enhances their immunogenicity: causes and mitigation strategies Lundahl, Mimmi L. E. Fogli, Silvia Colavita, Paula E. Scanlan, Eoin M. RSC Chem Biol Chemistry Protein aggregation in biotherapeutics has been identified to increase immunogenicity, leading to immune-mediated adverse effects, such as severe allergic responses including anaphylaxis. The induction of anti-drug antibodies (ADAs) moreover enhances drug clearance rates, and can directly block therapeutic function. In this review, identified immune activation mechanisms triggered by protein aggregates are discussed, as well as physicochemical properties of aggregates, such as size and shape, which contribute to immunogenicity. Furthermore, factors which contribute to protein stability and aggregation are considered. Lastly, with these factors in mind, we encourage an innovative and multidisciplinary approach with regard to further research in the field, with the overall aim to avoid immunogenic aggregation in future drug development. RSC 2021-05-04 /pmc/articles/PMC8341748/ /pubmed/34458822 http://dx.doi.org/10.1039/d1cb00067e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Lundahl, Mimmi L. E.
Fogli, Silvia
Colavita, Paula E.
Scanlan, Eoin M.
Aggregation of protein therapeutics enhances their immunogenicity: causes and mitigation strategies
title Aggregation of protein therapeutics enhances their immunogenicity: causes and mitigation strategies
title_full Aggregation of protein therapeutics enhances their immunogenicity: causes and mitigation strategies
title_fullStr Aggregation of protein therapeutics enhances their immunogenicity: causes and mitigation strategies
title_full_unstemmed Aggregation of protein therapeutics enhances their immunogenicity: causes and mitigation strategies
title_short Aggregation of protein therapeutics enhances their immunogenicity: causes and mitigation strategies
title_sort aggregation of protein therapeutics enhances their immunogenicity: causes and mitigation strategies
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8341748/
https://www.ncbi.nlm.nih.gov/pubmed/34458822
http://dx.doi.org/10.1039/d1cb00067e
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