调节性B细胞
白细胞介素10
免疫系统
细胞生物学
癌症研究
生物
免疫学
作者
Zheng Wang,Qiong Cheng,Ke Tang,Yanling Sun,Keke Zhang,Yi Zhang,Shunqun Luo,Yi Zhang,Duyun Ye,Bo Huang
出处
期刊:Cancer Letters
[Elsevier]
日期:2015-05-12
卷期号:364 (2): 118-124
被引量:73
标识
DOI:10.1016/j.canlet.2015.04.030
摘要
Lipoxin A4 (LXA4), an arachidonic acid-derived anti-inflammatory lipid mediator, shows anti-tumor potential by regulating tumor immune microenvironments. However, the underlying molecular and cellular basis of this function remains unclear. IL-10-producing B (Breg) cells display tumor-promoting effects by negatively regulating anti-tumor immunity. Here we show that LXA4 inhibits tumor growth by suppressing the generation of Breg cells in tumor-bearing mice. The administration of LXA4 inhibited the induction of Breg cells. Breg cell deficiency, in turn, resulted in LXA4 losing its anti-tumor properties. Intriguingly, regulatory T (Treg) cells also had a role in this process. Targeting Breg cells by LXA4 decreased the number of Treg cells in draining lymph nodes and tumor tissues as well as enhanced cytotoxic T cell activities. In addition, we further demonstrated that LXA4 inhibited Breg cells through its dephosphorylating STAT3 and ERK. These findings unveil a new anti-tumor mechanism underlying LXA4 targeting Breg cells with potential clinical applications.
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