Departamento de Inmunología y Oncología, Centro Nacional de Biotecnología/CSIC, Darwin 3, 28049 Madrid, Spain.
Departamento de Inmunología y Oncología, Centro Nacional de Biotecnología/CSIC, Darwin 3, 28049 Madrid, Spain.
Immunity. 2017 Jun 20;46(6):1059-1072.e4. doi: 10.1016/j.immuni.2017.05.009.
Neutrophils play a crucial role in defense against systemic candidiasis, a disease associated with a high mortality rate in patients receiving immunosuppressive therapy, although the early immune mechanisms that boost the candidacidal activity of neutrophils remain to be defined in depth. Here, we used a murine model of systemic candidiasis to explore the role of inflammatory Ly6C monocytes in NK cell-mediated neutrophil activation during the innate immune response against C. albicans. We found that efficient anti-Candida immunity required a collaborative response between the spleen and kidney, which relied on type I interferon-dependent IL-15 production by spleen inflammatory Ly6C monocytes to drive efficient activation and GM-CSF release by spleen NK cells; this in turn was necessary to boost the Candida killing potential of kidney neutrophils. Our findings unveil a role for IL-15 as a critical mediator in defense against systemic candidiasis and hold promise for the design of IL-15-based antifungal immunotherapies.
中性粒细胞在防御系统性念珠菌病方面发挥着关键作用,系统性念珠菌病是一种与接受免疫抑制治疗的患者死亡率高相关的疾病,尽管增强中性粒细胞杀念珠菌活性的早期免疫机制仍有待深入定义。在这里,我们使用系统性念珠菌病的小鼠模型来探索炎症性 Ly6C 单核细胞在 NK 细胞介导的中性粒细胞活化中的作用,这种活化发生于针对 C. albicans 的固有免疫反应中。我们发现,有效的抗念珠菌免疫需要脾脏和肾脏的协同反应,这依赖于脾脏炎症性 Ly6C 单核细胞产生的 I 型干扰素依赖性 IL-15,从而有效地激活和 GM-CSF 释放由脾脏 NK 细胞;这反过来对于增强肾脏中性粒细胞的杀念珠菌能力是必要的。我们的研究结果揭示了 IL-15 作为防御系统性念珠菌病的关键介质的作用,并为基于 IL-15 的抗真菌免疫治疗的设计提供了希望。