FOXP3型
过继性细胞移植
肺纤维化
免疫学
CCR2型
纤维化
医学
T细胞
免疫系统
支气管肺泡灌洗
白细胞介素2受体
肺
发病机制
特发性肺纤维化
趋化因子
病理
趋化因子受体
内科学
作者
Katrin Milger,Yingyan Yu,Eva Brudy,Martin Irmler,Alla Skapenko,Michael Mayinger,Mareike Lehmann,Johannes Beckers,Frank Reichenberger,Jürgen Behr,Oliver Eickelberg,Mélanie Königshoff,Susanne Krauss‐Etschmann
出处
期刊:Thorax
[BMJ]
日期:2017-08-05
卷期号:72 (11): 1007-1020
被引量:71
标识
DOI:10.1136/thoraxjnl-2016-208423
摘要
Pulmonary CCR2+CD4+ T cells are immunosuppressive, and could attenuate lung inflammation and fibrosis. Therapeutic strategies completely abrogating CCR2-dependent signalling will therefore also eliminate cell populations with protective roles in fibrotic lung disease. This emphasises the need for a detailed understanding of the functions of immune cell subsets in fibrotic lung disease.
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