Role of CD4<sup>+</sup> T Cells in Allergic Airway Diseases: Learning from Murine Models

The essential contribution of CD4<sup>+</sup> T cells in allergic airway diseases has been demonstrated, especially by using various murine models of antigen-induced airway inflammation. In addition to antigen-immunized mouse models employing mast cell-deficient mice and CD4<sup>+&...

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Main Authors: Kento Miura, Kimiko Inoue, Atsuo Ogura, Osamu Kaminuma
Format: Article
Language:English
Published: MDPI AG 2020-10-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/20/7480
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spelling doaj-c65f1a2180854578a7918cff62f897302020-11-25T03:56:16ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-10-01217480748010.3390/ijms21207480Role of CD4<sup>+</sup> T Cells in Allergic Airway Diseases: Learning from Murine ModelsKento Miura0Kimiko Inoue1Atsuo Ogura2Osamu Kaminuma3Department of Disease Model, Research Institute of Radiation Biology and Medicine, Hiroshima University, Hiroshima 734-8553, JapanRIKEN BioResource Research Center, Ibaraki 305-0074, JapanRIKEN BioResource Research Center, Ibaraki 305-0074, JapanDepartment of Disease Model, Research Institute of Radiation Biology and Medicine, Hiroshima University, Hiroshima 734-8553, JapanThe essential contribution of CD4<sup>+</sup> T cells in allergic airway diseases has been demonstrated, especially by using various murine models of antigen-induced airway inflammation. In addition to antigen-immunized mouse models employing mast cell-deficient mice and CD4<sup>+</sup> T cell-depleting procedure, antigen-specific CD4<sup>+</sup> T cell transfer models have revealed the possible development of allergic inflammation solely dependent on CD4<sup>+</sup> T cells. Regardless of the classical Th1/Th2 theory, various helper T cell subsets have the potential to induce different types of allergic inflammation. T cell receptor (TCR)-transgenic (Tg) mice have been used for investigating T cell-mediated immune responses. Besides, we have recently generated cloned mice from antigen-specific CD4<sup>+</sup> T cells through somatic cell nuclear transfer. In contrast to TCR-Tg mice that express artificially introduced TCR, the cloned mice express endogenously regulated antigen-specific TCR. Upon antigen exposure, the mite antigen-reactive T cell-cloned mice displayed strong airway inflammation accompanied by bronchial hyperresponsiveness in a short time period. Antigen-specific CD4<sup>+</sup> T cell-cloned mice are expected to be useful for investigating the detailed role of CD4<sup>+</sup> T cells in various allergic diseases and for evaluating novel anti-allergic drugs.https://www.mdpi.com/1422-0067/21/20/7480allergyairway inflammationCD4<sup>+</sup> T cellsomatic cell nuclear transferT-cell receptor
collection DOAJ
language English
format Article
sources DOAJ
author Kento Miura
Kimiko Inoue
Atsuo Ogura
Osamu Kaminuma
spellingShingle Kento Miura
Kimiko Inoue
Atsuo Ogura
Osamu Kaminuma
Role of CD4<sup>+</sup> T Cells in Allergic Airway Diseases: Learning from Murine Models
International Journal of Molecular Sciences
allergy
airway inflammation
CD4<sup>+</sup> T cell
somatic cell nuclear transfer
T-cell receptor
author_facet Kento Miura
Kimiko Inoue
Atsuo Ogura
Osamu Kaminuma
author_sort Kento Miura
title Role of CD4<sup>+</sup> T Cells in Allergic Airway Diseases: Learning from Murine Models
title_short Role of CD4<sup>+</sup> T Cells in Allergic Airway Diseases: Learning from Murine Models
title_full Role of CD4<sup>+</sup> T Cells in Allergic Airway Diseases: Learning from Murine Models
title_fullStr Role of CD4<sup>+</sup> T Cells in Allergic Airway Diseases: Learning from Murine Models
title_full_unstemmed Role of CD4<sup>+</sup> T Cells in Allergic Airway Diseases: Learning from Murine Models
title_sort role of cd4<sup>+</sup> t cells in allergic airway diseases: learning from murine models
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2020-10-01
description The essential contribution of CD4<sup>+</sup> T cells in allergic airway diseases has been demonstrated, especially by using various murine models of antigen-induced airway inflammation. In addition to antigen-immunized mouse models employing mast cell-deficient mice and CD4<sup>+</sup> T cell-depleting procedure, antigen-specific CD4<sup>+</sup> T cell transfer models have revealed the possible development of allergic inflammation solely dependent on CD4<sup>+</sup> T cells. Regardless of the classical Th1/Th2 theory, various helper T cell subsets have the potential to induce different types of allergic inflammation. T cell receptor (TCR)-transgenic (Tg) mice have been used for investigating T cell-mediated immune responses. Besides, we have recently generated cloned mice from antigen-specific CD4<sup>+</sup> T cells through somatic cell nuclear transfer. In contrast to TCR-Tg mice that express artificially introduced TCR, the cloned mice express endogenously regulated antigen-specific TCR. Upon antigen exposure, the mite antigen-reactive T cell-cloned mice displayed strong airway inflammation accompanied by bronchial hyperresponsiveness in a short time period. Antigen-specific CD4<sup>+</sup> T cell-cloned mice are expected to be useful for investigating the detailed role of CD4<sup>+</sup> T cells in various allergic diseases and for evaluating novel anti-allergic drugs.
topic allergy
airway inflammation
CD4<sup>+</sup> T cell
somatic cell nuclear transfer
T-cell receptor
url https://www.mdpi.com/1422-0067/21/20/7480
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