PI3K inhibition in inflammation: Toward tailored therapies for specific diseases

被引:111
作者
Ghigo, Alessandra [1 ]
Damilano, Federico [1 ]
Braccini, Laura [1 ]
Hirsch, Emilio [1 ]
机构
[1] Univ Turin, Ctr Mol Biotechnol, I-10126 Turin, Italy
关键词
allergy; atherosclerosis; COPD; inflammation; rheumatoid arthritis; PI3K; myocardial infarction; systemic lupus erythematosus; T-CELL DEVELOPMENT; PHOSPHOINOSITIDE 3-KINASE P110-DELTA; PHOSPHATIDYLINOSITOL; 3-KINASE; RHEUMATOID-ARTHRITIS; B-CELL; REGULATORY SUBUNIT; CUTTING EDGE; IN-VIVO; NEUTROPHIL TRAFFICKING; AIRWAY INFLAMMATION;
D O I
10.1002/bies.200900150
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the past decade, the availability of genetically modified animals has enabled the discovery of interesting roles for phosphatidylinositol 3-kinase-gamma (PI3K gamma) and -delta (PI3K delta) in different cell types orchestrating innate and adaptive immune responses. Therefore, these PI3K isoforms appear to be attractive drug targets for the treatment of diseases caused by unrestrained immune reactions. Currently, pharmacological targeting of PI3K gamma and/or PI3K delta represents one of the most promising challenges for companies interested in the development of novel safe treatments for inflammatory diseases. In this review we provide a general outline of PI3K gamma- and PI3K delta-specific functions in distinct subsets of inflammatory cells. We also discuss the therapeutic impact of novel compounds targeting PI3K gamma, PI3K delta or both, in mouse models of autoimmune disorders (systemic lupus erythematosus (SLE) and rheumatoid arthritis), respiratory diseases (allergic asthma and chronic obstructive pulmonary disease) and cardiovascular dysfunctions (atherosclerosis and myocardial infarction).
引用
收藏
页码:185 / 196
页数:12
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