The pronounced lung lesions developing in LATY136F knock-in mice mimic human IgG4-related lung disease

LATY136F 基因敲入小鼠出现的明显肺病变与人类 IgG4 相关肺病相似

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作者:Yuko Waseda, Kazunori Yamada, Keishi Mizuguchi, Kiyoaki Ito, Satoshi Watanabe, Masahiko Zuka, Tamotsu Ishizuka, Marie Malissen, Bernard Malissen, Mitsuhiro Kawano, Shoko Matsui

Conclusions

LATY136F knock-in mice constitute an appropriate model of lung lesions in IgG4-RD.

Methods

Lung tissue samples from LATY136F knock-in mice (LAT) and wild-type mice (WT) were immunostained for IgG1 and obtained for pathological evaluation, and cell fractions and cytokine levels in broncho-alveolar lavage fluid (BALF) were analyzed.

Results

In the LAT group, IgG1-positive inflammatory cells increased starting at 4 weeks of age and peaked at 10 weeks of age. The total cell count and percentage of lymphocytes increased significantly in BALF in the LAT group compared to the WT group. In BALF, Th2-dominant cytokines and transforming growth factor-β were also increased. In the LAT group, marked inflammation around broncho-vascular bundles peaked at 10 weeks of age. After 10 weeks, fibrosis around broncho-vascular bundles and bronchiectasis were observed in LATY136F knock-in mice but not WT mice. Conclusions: LATY136F knock-in mice constitute an appropriate model of lung lesions in IgG4-RD.

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