共 90 条
Pegylated IL-10 induces cancer immunity
被引:55
作者:

Mumm, John B.
论文数: 0 引用数: 0
h-index: 0
机构:
ARMO Biosci, Redwood City, CA USA ARMO Biosci, Redwood City, CA USA

Oft, Martin
论文数: 0 引用数: 0
h-index: 0
机构:
ARMO Biosci, Redwood City, CA USA ARMO Biosci, Redwood City, CA USA
机构:
[1] ARMO Biosci, Redwood City, CA USA
来源:
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.
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收藏
页码:623 / 631
页数:9
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