Department of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.
University of Basel, Department of Biomedicine, Basel, Switzerland.
Nat Rev Immunol. 2022 Nov;22(11):687-700. doi: 10.1038/s41577-022-00701-8. Epub 2022 Mar 23.
Over the past two decades, new insights have positioned phosphoinositide 3-kinase-γ (PI3Kγ) as a context-dependent modulator of immunity and inflammation. Recent advances in protein structure determination and drug development have allowed for generation of highly specific PI3Kγ inhibitors, with the first now in clinical trials for several oncology indications. Recently, a monogenic immune disorder caused by PI3Kγ deficiency was discovered in humans and modelled in mice. Human inactivated PI3Kγ syndrome confirms the immunomodulatory roles of PI3Kγ and strengthens newly defined roles of this molecule in modulating inflammatory cytokine release in macrophages. Here, we review the functions of PI3Kγ in the immune system and discuss how our understanding of its potential as a therapeutic target has evolved.
在过去的二十年中,新的研究进展将磷酸肌醇 3-激酶-γ(PI3Kγ)定位为免疫和炎症的一种依赖于上下文的调节剂。蛋白质结构测定和药物开发的最新进展使得能够产生高度特异性的 PI3Kγ 抑制剂,第一个现在正在针对几种肿瘤适应症进行临床试验。最近,在人类中发现了一种由 PI3Kγ 缺乏引起的单基因免疫性疾病,并在小鼠中进行了建模。人类失活的 PI3Kγ 综合征证实了 PI3Kγ 的免疫调节作用,并加强了该分子在调节巨噬细胞中炎症细胞因子释放方面的新定义作用。在这里,我们回顾了 PI3Kγ 在免疫系统中的功能,并讨论了我们对其作为治疗靶点的潜力的理解是如何发展的。