【摘 要】
：
Background: Idiopathic pulmonary fibrosis (IPF) is a devastating treatment-refractory interstitial lung disease of unknown origin.Although the pathogenic me
【机 构】
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Department of Immunology,College of Basic Medical Sciences,Jilin University
【出 处】
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中国免疫学会第十届全国免疫学学术大会
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Background: Idiopathic pulmonary fibrosis (IPF) is a devastating treatment-refractory interstitial lung disease of unknown origin.Although the pathogenic mechanism of IPF is not fully understood, lung histology and bronchoalveolar lavage (BAL) show inflammatory cytology, including neutrophils, lymphocytes, macrophages, etc., which are thought to contribute to fibrogenesis.
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