التفاصيل البيبلوغرافية
| العنوان: |
An IL-17-EGFR-TRAF4 axis contributes to the alleviation of lung inflammation in severe influenza |
| المؤلفون: |
Avijit Dutta, Chen-Yiu Hung, Tse-Ching Chen, Sung-Han Hsiao, Chia-Shiang Chang, Yung-Chang Lin, Chun-Yen Lin, Ching-Tai Huang |
| المصدر: |
Communications Biology, Vol 6, Iss 1, Pp 1-14 (2023) |
| بيانات النشر: |
Nature Portfolio, 2023. |
| سنة النشر: |
2023 |
| المجموعة: |
LCC:Biology (General) |
| مصطلحات موضوعية: |
Biology (General), QH301-705.5 |
| الوصف: |
Abstract Excessive inflammation is a postulated cause of severe disease and death in respiratory virus infections. In response to severe influenza virus infection, adoptively transferred naïve hemagglutinin-specific CD4+ T cells from CD4+ TCR-transgenic 6.5 mice drive an IFN-γ-producing Th1 response in wild-type mice. It helps in virus clearance but also causes collateral damage and disease aggravation. The donor 6.5 mice have all the CD4+ T cells with TCR specificity toward influenza hemagglutinin. Still, the infected 6.5 mice do not suffer from robust inflammation and grave outcome. The initial Th1 response wanes with time, and a prominent Th17 response of recent thymic emigrants alleviates inflammation and bestows protection in 6.5 mice. Our results suggest that viral neuraminidase-activated TGF-β of the Th1 cells guides the Th17 evolution, and IL-17 signaling through the non-canonical IL-17 receptor EGFR activates the scaffold protein TRAF4 more than TRAF6 during alleviation of lung inflammation in severe influenza. |
| نوع الوثيقة: |
article |
| وصف الملف: |
electronic resource |
| اللغة: |
English |
| تدمد: |
2399-3642 |
| Relation: |
https://doaj.org/toc/2399-3642 |
| DOI: |
10.1038/s42003-023-04982-0 |
| URL الوصول: |
https://doaj.org/article/60134cc7d05841eebd9a2bd4fc3360f4 |
| رقم الانضمام: |
edsdoj.60134cc7d05841eebd9a2bd4fc3360f4 |
| قاعدة البيانات: |
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