Pegylated IL-10 induces cancer immunity

被引:55
作者
Mumm, John B. [1 ]
Oft, Martin [1 ]
机构
[1] ARMO Biosci, Redwood City, CA USA
关键词
cancer immune therapy; CD8(+) T cells; cytotoxic T cells; IFN-gamma; major histocompatibility complex; pegylated-IL-10; OXYSTEROL-BINDING-PROTEIN; SAC1 LIPID PHOSPHATASE; 4-KINASE II-ALPHA; PHOSPHATIDYLINOSITOL; 4-KINASE; PLASMA-MEMBRANE; MYOSIN-V; GOLGI LOCALIZATION; SECRETORY VESICLES; GROWTH-CONTROL; KINASE;
D O I
10.1002/bies.201300004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Recently, the development of several strategies based on immunotherapy has raised hopes for a more promising way to treat cancer patients. Here, we describe how interleukin (IL)-10, a seemingly unlikely candidate, stimulates the immune system in a particularly efficacious way. IL-10, an omnipotent anti-inflammatory cytokine, delivers an equally potent immune stimulation in the context of CD8(+) T cells and tumor immunity. By activation of tumor-resident, tumor-specific CD8(+) T cells, pegylated IL-10 can induce rejection of large and meta-stasizing tumors in mice. Here, we summarize the mechanisms of action of IL-10, the reasons why the mechanisms may be crucial for the treatment of cancer patients, and the rationale for applying pegylated IL-10 in the clinic.
引用
收藏
页码:623 / 631
页数:9
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