Role of interleukins in the pathogenesis of pulmonary fibrosis
Abstract Interleukins, a group of cytokines participating in inflammation and immune response, are proved to be involved in the formation and development of pulmonary fibrosis. In this article, we reviewed the relationship between interleukins and pulmonary fibrosis from the clinical, animal, as wel...
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2021-03-01
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Series: | Cell Death Discovery |
Online Access: | https://doi.org/10.1038/s41420-021-00437-9 |
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doaj-c93691b3b151445eb7c4373250c3b9d12021-03-21T12:49:46ZengNature Publishing GroupCell Death Discovery2058-77162021-03-017111010.1038/s41420-021-00437-9Role of interleukins in the pathogenesis of pulmonary fibrosisYi Xin She0Qing Yang Yu1Xiao Xiao Tang2State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityState Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityState Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityAbstract Interleukins, a group of cytokines participating in inflammation and immune response, are proved to be involved in the formation and development of pulmonary fibrosis. In this article, we reviewed the relationship between interleukins and pulmonary fibrosis from the clinical, animal, as well as cellular levels, and discussed the underlying mechanisms in vivo and in vitro. Despite the effects of interleukin-targeted treatment on experimental pulmonary fibrosis, clinical applications are lacking and unsatisfactory. We conclude that intervening in one type of interleukins with similar functions in IPF may not be enough to stop the development of fibrosis as it involves a complex network of regulation mechanisms. Intervening interleukins combined with other existing therapy or targeting interleukins affecting multiple cells/with different functions at the same time may be one of the future directions. Furthermore, the intervention time is critical as some interleukins play different roles at different stages. Further elucidation on these aspects would provide new perspectives on both the pathogenesis mechanism, as well as the therapeutic strategy and drug development.https://doi.org/10.1038/s41420-021-00437-9 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yi Xin She Qing Yang Yu Xiao Xiao Tang |
spellingShingle |
Yi Xin She Qing Yang Yu Xiao Xiao Tang Role of interleukins in the pathogenesis of pulmonary fibrosis Cell Death Discovery |
author_facet |
Yi Xin She Qing Yang Yu Xiao Xiao Tang |
author_sort |
Yi Xin She |
title |
Role of interleukins in the pathogenesis of pulmonary fibrosis |
title_short |
Role of interleukins in the pathogenesis of pulmonary fibrosis |
title_full |
Role of interleukins in the pathogenesis of pulmonary fibrosis |
title_fullStr |
Role of interleukins in the pathogenesis of pulmonary fibrosis |
title_full_unstemmed |
Role of interleukins in the pathogenesis of pulmonary fibrosis |
title_sort |
role of interleukins in the pathogenesis of pulmonary fibrosis |
publisher |
Nature Publishing Group |
series |
Cell Death Discovery |
issn |
2058-7716 |
publishDate |
2021-03-01 |
description |
Abstract Interleukins, a group of cytokines participating in inflammation and immune response, are proved to be involved in the formation and development of pulmonary fibrosis. In this article, we reviewed the relationship between interleukins and pulmonary fibrosis from the clinical, animal, as well as cellular levels, and discussed the underlying mechanisms in vivo and in vitro. Despite the effects of interleukin-targeted treatment on experimental pulmonary fibrosis, clinical applications are lacking and unsatisfactory. We conclude that intervening in one type of interleukins with similar functions in IPF may not be enough to stop the development of fibrosis as it involves a complex network of regulation mechanisms. Intervening interleukins combined with other existing therapy or targeting interleukins affecting multiple cells/with different functions at the same time may be one of the future directions. Furthermore, the intervention time is critical as some interleukins play different roles at different stages. Further elucidation on these aspects would provide new perspectives on both the pathogenesis mechanism, as well as the therapeutic strategy and drug development. |
url |
https://doi.org/10.1038/s41420-021-00437-9 |
work_keys_str_mv |
AT yixinshe roleofinterleukinsinthepathogenesisofpulmonaryfibrosis AT qingyangyu roleofinterleukinsinthepathogenesisofpulmonaryfibrosis AT xiaoxiaotang roleofinterleukinsinthepathogenesisofpulmonaryfibrosis |
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