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体内成像研究炎症小体激活揭示了被膜下巨噬细胞爆发反应,该反应可动员先天和适应性免疫。

In vivo imaging of inflammasome activation reveals a subcapsular macrophage burst response that mobilizes innate and adaptive immunity.

机构信息

Dynamics of Immune Responses Unit, Institut Pasteur, Paris, France.

Institut National de la Santé et de la Recherche Médicale U668, Paris, France.

出版信息

Nat Med. 2016 Jan;22(1):64-71. doi: 10.1038/nm.4016. Epub 2015 Dec 21.

Abstract

The inflammasome is activated in response to a variety of pathogens and has an important role in shaping adaptive immunity, yet the spatiotemporal orchestration of inflammasome activation in vivo and the mechanisms by which it promotes an effective immune response are not fully understood. Using an in vivo reporter to visualize inflammasome assembly, we establish the distribution, kinetics and propagation of the inflammasome response to a local viral infection. We show that modified vaccinia Ankara virus induces inflammasome activation in subcapsular sinus (SCS) macrophages, which is immediately followed by cell death and release of extracellular ASC specks. This transient inflammasome signaling in the lymph node generates a robust influx of inflammatory cells and mobilizes T cells from the circulation to increase the magnitude of T cell responses. We propose that after infection, SCS macrophages deliver a burst response of inflammasome activity and cell death that translates into the broadening of T cell responses, identifying an important aspect of inflammasome-driven vaccination strategies.

摘要

炎症小体在响应各种病原体时被激活,在塑造适应性免疫方面发挥着重要作用,但炎症小体在体内的激活的时空协调以及它促进有效免疫反应的机制尚未完全了解。我们使用体内报告基因来可视化炎症小体的组装,从而确定了局部病毒感染时炎症小体反应的分布、动力学和传播。我们发现改良安卡拉牛痘病毒在被膜下窦(SCS)巨噬细胞中诱导炎症小体激活,随后立即发生细胞死亡和细胞外 ASC 斑点的释放。淋巴结中这种短暂的炎症小体信号转导会引发大量炎症细胞的涌入,并从循环中动员 T 细胞,以增加 T 细胞反应的强度。我们提出,感染后,SCS 巨噬细胞会爆发炎症小体活性和细胞死亡,从而扩大 T 细胞反应,这是炎症小体驱动疫苗接种策略的一个重要方面。

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