Could interferon-gamma be a therapeutic target for treating heart failure?

被引:77
作者
Levick, Scott P. [1 ]
Goldspink, Paul H. [2 ]
机构
[1] Med Coll Wisconsin, Ctr Cardiovasc, Dept Pharmacol & Toxicol, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Physiol, Cardiovasc Ctr, Milwaukee, WI 53226 USA
基金
美国国家卫生研究院;
关键词
Interferon-gamma; Heart failure; Hypertrophy; Fibrosis; Inflammation; PROTEIN-KINASE-C; SIGNAL-TRANSDUCTION PATHWAY; TUMOR-NECROSIS-FACTOR; IFN-GAMMA; PHOSPHATIDYLINOSITOL; 3-KINASE; DILATED CARDIOMYOPATHY; MYOCARDIAL FIBROSIS; T-LYMPHOCYTES; PKC-EPSILON; GENE;
D O I
10.1007/s10741-013-9393-8
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The cytokine interferon-gamma (IFN-gamma) is the only known member of the type II family of interferons, and as such, binds to its own distinct receptor. It is important in host defense against infection, as well as adaptive immune responses. While a wide array of cytokines are known to be involved in adverse remodeling of the heart and the progression to heart failure, the role of IFN-gamma is unclear. Recent evidence from clinical studies, animal models of myocarditis and hypertension, as well as isolated cell studies, provide conflicting data as to whether IFN-gamma is pathological or protective in the heart. Thus, it is important to highlight these discrepant findings so that areas of future investigation can be identified to more clearly determine the precise role of IFN-gamma in the heart. Accordingly, this review will (1) discuss the source of IFN-gamma in the diseased heart; (2) summarize the data from animal studies; (3) discuss the effects of IFN-gamma on isolated cardiac fibroblasts and cardiomyocytes; (4) identify signaling mechanisms that may be invoked by IFN-gamma in the heart; and (5) present the clinical evidence supporting a role for IFN-gamma in heart failure.
引用
收藏
页码:227 / 236
页数:10
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