Molecular Biotechnology Center, University of Torino, Via Nizza 52, 10126 Torino, Italy.
Bioessays. 2010 Mar;32(3):185-196. doi: 10.1002/bies.200900150.
In the past decade, the availability of genetically modified animals has enabled the discovery of interesting roles for phosphatidylinositol 3-kinase-gamma (PI3Kgamma) and -delta (PI3Kdelta) 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 PI3Kgamma and/or PI3Kdelta 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 PI3Kgamma- and PI3Kdelta-specific functions in distinct subsets of inflammatory cells. We also discuss the therapeutic impact of novel compounds targeting PI3Kgamma, PI3Kdelta 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).
在过去的十年中,基因修饰动物的出现使人们发现了磷脂酰肌醇 3-激酶-γ(PI3Kγ)和 -δ(PI3Kδ)在不同类型的细胞中协调先天和适应性免疫反应的有趣作用。因此,这些 PI3K 同工型似乎是治疗由不受控制的免疫反应引起的疾病的有吸引力的药物靶点。目前,药理学靶向 PI3Kγ 和/或 PI3Kδ 是对开发新型安全治疗炎症性疾病感兴趣的公司面临的最有希望的挑战之一。在这篇综述中,我们提供了 PI3Kγ 和 PI3Kδ 在不同炎症细胞亚群中的特异性功能的概述。我们还讨论了靶向 PI3Kγ、PI3Kδ 或两者的新型化合物在自身免疫性疾病(系统性红斑狼疮(SLE)和类风湿性关节炎)、呼吸道疾病(过敏性哮喘和慢性阻塞性肺疾病)和心血管功能障碍(动脉粥样硬化和心肌梗死)的小鼠模型中的治疗效果。