细胞毒性T细胞
化学
癌症研究
生物
细胞生物学
分子生物学
生物化学
体外
作者
Ming Xiang,Tingting Liu,Wanyue Tan,Hongyu Ren,Hua Li,Junjun Liu,Hui Cao,Qi Cheng,Xiulan Liu,Hucheng Zhu,Yali Tuo,Jianping Wang,Yonghui Zhang
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2016-09-17
卷期号:64 (6): 2135-2150
被引量:53
摘要
KD treatment elicits immunosuppression against autoimmune liver injury by targeting VEGFR2, followed by diminishing the cross-talk of metabolism-related PI3K-AKT and inflammation-related JAK2-STAT3 pathways, and thereby disrupts DC-induced cross-priming of CD8+ T cell responses. (Hepatology 2016;64:2135-2150).
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