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Mimicking Antigen-Driven Asthma in Rodent Models—How Close Can We Get?

Asthma is a heterogeneous disease with increasing prevalence worldwide characterized by chronic airway inflammation, increased mucus secretion and bronchial hyperresponsiveness. The phenotypic heterogeneity among asthmatic patients is accompanied by different endotypes, mainly Type 2 or non-Type 2....

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Autores principales: Alessandrini, Francesca, Musiol, Stephanie, Schneider, Evelyn, Blanco-Pérez, Frank, Albrecht, Melanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555606/
https://www.ncbi.nlm.nih.gov/pubmed/33101301
http://dx.doi.org/10.3389/fimmu.2020.575936
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author Alessandrini, Francesca
Musiol, Stephanie
Schneider, Evelyn
Blanco-Pérez, Frank
Albrecht, Melanie
author_facet Alessandrini, Francesca
Musiol, Stephanie
Schneider, Evelyn
Blanco-Pérez, Frank
Albrecht, Melanie
author_sort Alessandrini, Francesca
collection PubMed
description Asthma is a heterogeneous disease with increasing prevalence worldwide characterized by chronic airway inflammation, increased mucus secretion and bronchial hyperresponsiveness. The phenotypic heterogeneity among asthmatic patients is accompanied by different endotypes, mainly Type 2 or non-Type 2. To investigate the pathomechanism of this complex disease many animal models have been developed, each trying to mimic specific aspects of the human disease. Rodents have classically been employed in animal models of asthma. The present review provides an overview of currently used Type 2 vs. non-Type 2 rodent asthma models, both acute and chronic. It further assesses the methods used to simulate disease development and exacerbations as well as to quantify allergic airway inflammation, including lung physiologic, cellular and molecular immunologic responses. Furthermore, the employment of genetically modified animals, which provide an in-depth understanding of the role of a variety of molecules, signaling pathways and receptors implicated in the development of this disease as well as humanized models of allergic inflammation, which have been recently developed to overcome differences between the rodent and human immune systems, are discussed. Nevertheless, differences between mice and humans should be carefully considered and limits of extrapolation should be wisely taken into account when translating experimental results into clinical use.
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spelling pubmed-75556062020-10-22 Mimicking Antigen-Driven Asthma in Rodent Models—How Close Can We Get? Alessandrini, Francesca Musiol, Stephanie Schneider, Evelyn Blanco-Pérez, Frank Albrecht, Melanie Front Immunol Immunology Asthma is a heterogeneous disease with increasing prevalence worldwide characterized by chronic airway inflammation, increased mucus secretion and bronchial hyperresponsiveness. The phenotypic heterogeneity among asthmatic patients is accompanied by different endotypes, mainly Type 2 or non-Type 2. To investigate the pathomechanism of this complex disease many animal models have been developed, each trying to mimic specific aspects of the human disease. Rodents have classically been employed in animal models of asthma. The present review provides an overview of currently used Type 2 vs. non-Type 2 rodent asthma models, both acute and chronic. It further assesses the methods used to simulate disease development and exacerbations as well as to quantify allergic airway inflammation, including lung physiologic, cellular and molecular immunologic responses. Furthermore, the employment of genetically modified animals, which provide an in-depth understanding of the role of a variety of molecules, signaling pathways and receptors implicated in the development of this disease as well as humanized models of allergic inflammation, which have been recently developed to overcome differences between the rodent and human immune systems, are discussed. Nevertheless, differences between mice and humans should be carefully considered and limits of extrapolation should be wisely taken into account when translating experimental results into clinical use. Frontiers Media S.A. 2020-09-30 /pmc/articles/PMC7555606/ /pubmed/33101301 http://dx.doi.org/10.3389/fimmu.2020.575936 Text en Copyright © 2020 Alessandrini, Musiol, Schneider, Blanco-Pérez and Albrecht. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Alessandrini, Francesca
Musiol, Stephanie
Schneider, Evelyn
Blanco-Pérez, Frank
Albrecht, Melanie
Mimicking Antigen-Driven Asthma in Rodent Models—How Close Can We Get?
title Mimicking Antigen-Driven Asthma in Rodent Models—How Close Can We Get?
title_full Mimicking Antigen-Driven Asthma in Rodent Models—How Close Can We Get?
title_fullStr Mimicking Antigen-Driven Asthma in Rodent Models—How Close Can We Get?
title_full_unstemmed Mimicking Antigen-Driven Asthma in Rodent Models—How Close Can We Get?
title_short Mimicking Antigen-Driven Asthma in Rodent Models—How Close Can We Get?
title_sort mimicking antigen-driven asthma in rodent models—how close can we get?
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555606/
https://www.ncbi.nlm.nih.gov/pubmed/33101301
http://dx.doi.org/10.3389/fimmu.2020.575936
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