TY - JOUR
T1 - Innate Lymphoid Cells
T2 - A Promising New Regulator in Fibrotic Diseases
AU - Zhang, Yi
AU - Tang, Jun
AU - Tian, Zhiqiang
AU - van Velkinburgh, Jennifer C.
AU - Song, Jianxun
AU - Wu, Yuzhang
AU - Ni, Bing
N1 - Publisher Copyright:
© 2016, Copyright © Taylor & Francis Group, LLC.
PY - 2016/9/2
Y1 - 2016/9/2
N2 - Fibrosis is a consequence of chronic inflammation and the persistent accumulation of extracellular matrix, for which the cycle of tissue injury and repair becomes a predominant feature. Both the innate and adaptive immune systems play key roles in the progress of fibrosis. The recently identified subsets of innate lymphoid cells (ILCs), which are mainly localize to epithelial surfaces, have been characterized as regulators of chronic inflammation and tissue remodeling, representing a functional bridge between the innate and adaptive immunity. Moreover, recent research has implicated ILCs as potential contributing factors to several kinds of fibrosis diseases, such as hepatic fibrosis and pulmonary fibrosis. Here, we will summarize and discuss the key roles of ILCs and their related factors in fibrotic diseases and their potential for translation to the clinic.
AB - Fibrosis is a consequence of chronic inflammation and the persistent accumulation of extracellular matrix, for which the cycle of tissue injury and repair becomes a predominant feature. Both the innate and adaptive immune systems play key roles in the progress of fibrosis. The recently identified subsets of innate lymphoid cells (ILCs), which are mainly localize to epithelial surfaces, have been characterized as regulators of chronic inflammation and tissue remodeling, representing a functional bridge between the innate and adaptive immunity. Moreover, recent research has implicated ILCs as potential contributing factors to several kinds of fibrosis diseases, such as hepatic fibrosis and pulmonary fibrosis. Here, we will summarize and discuss the key roles of ILCs and their related factors in fibrotic diseases and their potential for translation to the clinic.
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U2 - 10.3109/08830185.2015.1068304
DO - 10.3109/08830185.2015.1068304
M3 - Review article
C2 - 26222510
AN - SCOPUS:84939478290
SN - 0883-0185
VL - 35
SP - 399
EP - 414
JO - International Reviews of Immunology
JF - International Reviews of Immunology
IS - 5
ER -