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Recent Advances in Allergy Research Using Humanized Mice

The prevalence rates of allergic diseases are increasing worldwide, particularly in industrial countries. To date, many mouse models have been generated for allergy research; studies conducted using these models have suggested the importance of cross-talk between immune cells and tissue-resident non...

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Autores principales: Ito, Ryoji, Maruoka, Shuichiro, Gon, Yasuhiro, Katano, Ikumi, Takahashi, Takeshi, Ito, Mamoru, Izuhara, Kenji, Nunomura, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600417/
https://www.ncbi.nlm.nih.gov/pubmed/31167385
http://dx.doi.org/10.3390/ijms20112740
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author Ito, Ryoji
Maruoka, Shuichiro
Gon, Yasuhiro
Katano, Ikumi
Takahashi, Takeshi
Ito, Mamoru
Izuhara, Kenji
Nunomura, Satoshi
author_facet Ito, Ryoji
Maruoka, Shuichiro
Gon, Yasuhiro
Katano, Ikumi
Takahashi, Takeshi
Ito, Mamoru
Izuhara, Kenji
Nunomura, Satoshi
author_sort Ito, Ryoji
collection PubMed
description The prevalence rates of allergic diseases are increasing worldwide, particularly in industrial countries. To date, many mouse models have been generated for allergy research; studies conducted using these models have suggested the importance of cross-talk between immune cells and tissue-resident non-immune cells in the onset of allergic diseases. However, there are several differences between the immune systems of rodents and humans, and human studies are limited. Thus, mice reconstituted with human immune cells are a novel tool for the preclinical evaluation of the efficacy and safety of developing drugs. Genetic technologies for generating humanized mice have improved markedly in recent years. In this review, we will discuss recent progress in allergy research using humanized mice and introduce our recent humanized mouse model of airway inflammation in human immune cells.
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spelling pubmed-66004172019-07-16 Recent Advances in Allergy Research Using Humanized Mice Ito, Ryoji Maruoka, Shuichiro Gon, Yasuhiro Katano, Ikumi Takahashi, Takeshi Ito, Mamoru Izuhara, Kenji Nunomura, Satoshi Int J Mol Sci Review The prevalence rates of allergic diseases are increasing worldwide, particularly in industrial countries. To date, many mouse models have been generated for allergy research; studies conducted using these models have suggested the importance of cross-talk between immune cells and tissue-resident non-immune cells in the onset of allergic diseases. However, there are several differences between the immune systems of rodents and humans, and human studies are limited. Thus, mice reconstituted with human immune cells are a novel tool for the preclinical evaluation of the efficacy and safety of developing drugs. Genetic technologies for generating humanized mice have improved markedly in recent years. In this review, we will discuss recent progress in allergy research using humanized mice and introduce our recent humanized mouse model of airway inflammation in human immune cells. MDPI 2019-06-04 /pmc/articles/PMC6600417/ /pubmed/31167385 http://dx.doi.org/10.3390/ijms20112740 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ito, Ryoji
Maruoka, Shuichiro
Gon, Yasuhiro
Katano, Ikumi
Takahashi, Takeshi
Ito, Mamoru
Izuhara, Kenji
Nunomura, Satoshi
Recent Advances in Allergy Research Using Humanized Mice
title Recent Advances in Allergy Research Using Humanized Mice
title_full Recent Advances in Allergy Research Using Humanized Mice
title_fullStr Recent Advances in Allergy Research Using Humanized Mice
title_full_unstemmed Recent Advances in Allergy Research Using Humanized Mice
title_short Recent Advances in Allergy Research Using Humanized Mice
title_sort recent advances in allergy research using humanized mice
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600417/
https://www.ncbi.nlm.nih.gov/pubmed/31167385
http://dx.doi.org/10.3390/ijms20112740
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