Center for Vaccine Biology and Immunology, Department of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY, USA.
Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Nat Immunol. 2019 Jan;20(1):64-72. doi: 10.1038/s41590-018-0250-8. Epub 2018 Nov 19.
Toxoplasma gondii is a common protozoan parasite that infects up to one third of the world's population. Notably, very little is known about innate immune sensing mechanisms for this obligate intracellular parasite by human cells. Here, by applying an unbiased biochemical screening approach, we show that human monocytes recognized the presence of T. gondii infection by detecting the alarmin S100A11 protein, which is released from parasite-infected cells via caspase-1-dependent mechanisms. S100A11 induced a potent chemokine response to T. gondii by engaging its receptor RAGE, and regulated monocyte recruitment in vivo by inducing expression of the chemokine CCL2. Our experiments reveal a sensing system for T. gondii by human cells that is based on the detection of infection-mediated release of S100A11 and RAGE-dependent induction of CCL2, a crucial chemokine required for host resistance to the parasite.
刚地弓形虫是一种常见的原生动物寄生虫,感染了世界上三分之一的人口。值得注意的是,人类细胞对这种专性细胞内寄生虫的先天免疫感应机制知之甚少。在这里,我们通过应用一种无偏见的生化筛选方法,表明人类单核细胞通过检测寄生虫感染细胞通过半胱天冬酶-1 依赖性机制释放的警报素 S100A11 来识别弓形虫感染的存在。S100A11 通过与受体 RAGE 结合诱导强烈的趋化因子反应,通过诱导趋化因子 CCL2 的表达来调节体内单核细胞的募集。我们的实验揭示了人类细胞对弓形虫的感应系统,该系统基于感染介导的 S100A11 释放的检测和 RAGE 依赖性 CCL2 的诱导,CCL2 是宿主抵抗寄生虫所必需的关键趋化因子。