Institut Pasteur, Université de Paris, Inserm U1223, Innate Immunity Unit, Paris, France.
Institut Pasteur, Université de Paris, Transcriptome and Epigenome Platform-Biomics Pole, Paris, France.
Science. 2022 Feb 25;375(6583):859-863. doi: 10.1126/science.aaz8777. Epub 2022 Feb 24.
Group 3 innate lymphoid cells (ILC3s) are innate immune effectors that contribute to host defense. Whether ILC3 functions are stably modified after pathogen encounter is unknown. Here, we assess the impact of a time-restricted enterobacterial challenge to long-term ILC3 activation in mice. We found that intestinal ILC3s persist for months in an activated state after exposure to . Upon rechallenge, these "trained" ILC3s proliferate, display enhanced interleukin-22 (IL-22) responses, and have a superior capacity to control infection compared with naïve ILC3s. Metabolic changes occur in -exposed ILC3s, but only trained ILC3s have an enhanced proliferative capacity that contributes to increased IL-22 production. Accordingly, a limited encounter with a pathogen can promote durable phenotypic and functional changes in intestinal ILC3s that contribute to long-term mucosal defense.
第三组固有淋巴细胞 (ILC3) 是先天免疫效应细胞,有助于宿主防御。在病原体接触后,ILC3 的功能是否会稳定改变尚不清楚。在这里,我们评估了对肠道上皮细胞进行限时肠杆菌挑战对小鼠长期 ILC3 激活的影响。我们发现,在接触 后,肠道 ILC3 会在激活状态下持续数月。再次挑战时,与幼稚 ILC3 相比,这些“训练有素”的 ILC3 增殖、显示出增强的白细胞介素-22 (IL-22) 反应,并且具有更好的控制感染的能力。在 暴露的 ILC3 中会发生代谢变化,但只有训练有素的 ILC3 才具有增强的增殖能力,有助于增加 IL-22 的产生。因此,与病原体的有限接触可以促进肠道 ILC3 中持久的表型和功能变化,有助于长期的黏膜防御。