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Crosstalk between ILC2s and Th2 CD4(+) T Cells in Lung Disease
Cytokine secretion, such as interleukin-4 (IL-4), IL-5, IL-9, IL-13, and amphiregulin (Areg), by type 2 innate lymphoid cells (ILC2s) is indispensable for homeostasis, remodeling/repairing tissue structure, inflammation, and tumor immunity. Often viewed as the innate cell surrogate of T helper type...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113865/ https://www.ncbi.nlm.nih.gov/pubmed/35592688 http://dx.doi.org/10.1155/2022/8871037 |
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author | Mi, Lan-lan Guo, Wei-wei |
author_facet | Mi, Lan-lan Guo, Wei-wei |
author_sort | Mi, Lan-lan |
collection | PubMed |
description | Cytokine secretion, such as interleukin-4 (IL-4), IL-5, IL-9, IL-13, and amphiregulin (Areg), by type 2 innate lymphoid cells (ILC2s) is indispensable for homeostasis, remodeling/repairing tissue structure, inflammation, and tumor immunity. Often viewed as the innate cell surrogate of T helper type 2 (Th2) cells, ILC2s not only secrete the same type 2 cytokines, but are also inextricably related to CD4(+)T cells in terms of cell origin and regulatory factors, bridging between innate and adaptive immunity. ILC2s interact with CD4(+)T cells to play a leading role in a variety of diseases through secretory factors. Here, we review the latest progress on ILC2s and CD4(+)T cells in the lung, the close relationship between the two, and their relevance in the lung disease and immunity. This literature review aids future research in pulmonary type 2 immune diseases and guides innovative treatment approaches for these diseases. |
format | Online Article Text |
id | pubmed-9113865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-91138652022-05-18 Crosstalk between ILC2s and Th2 CD4(+) T Cells in Lung Disease Mi, Lan-lan Guo, Wei-wei J Immunol Res Review Article Cytokine secretion, such as interleukin-4 (IL-4), IL-5, IL-9, IL-13, and amphiregulin (Areg), by type 2 innate lymphoid cells (ILC2s) is indispensable for homeostasis, remodeling/repairing tissue structure, inflammation, and tumor immunity. Often viewed as the innate cell surrogate of T helper type 2 (Th2) cells, ILC2s not only secrete the same type 2 cytokines, but are also inextricably related to CD4(+)T cells in terms of cell origin and regulatory factors, bridging between innate and adaptive immunity. ILC2s interact with CD4(+)T cells to play a leading role in a variety of diseases through secretory factors. Here, we review the latest progress on ILC2s and CD4(+)T cells in the lung, the close relationship between the two, and their relevance in the lung disease and immunity. This literature review aids future research in pulmonary type 2 immune diseases and guides innovative treatment approaches for these diseases. Hindawi 2022-05-10 /pmc/articles/PMC9113865/ /pubmed/35592688 http://dx.doi.org/10.1155/2022/8871037 Text en Copyright © 2022 Lan-lan Mi and Wei-wei Guo. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Mi, Lan-lan Guo, Wei-wei Crosstalk between ILC2s and Th2 CD4(+) T Cells in Lung Disease |
title | Crosstalk between ILC2s and Th2 CD4(+) T Cells in Lung Disease |
title_full | Crosstalk between ILC2s and Th2 CD4(+) T Cells in Lung Disease |
title_fullStr | Crosstalk between ILC2s and Th2 CD4(+) T Cells in Lung Disease |
title_full_unstemmed | Crosstalk between ILC2s and Th2 CD4(+) T Cells in Lung Disease |
title_short | Crosstalk between ILC2s and Th2 CD4(+) T Cells in Lung Disease |
title_sort | crosstalk between ilc2s and th2 cd4(+) t cells in lung disease |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113865/ https://www.ncbi.nlm.nih.gov/pubmed/35592688 http://dx.doi.org/10.1155/2022/8871037 |
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