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The Vaccine Adjuvant Chitosan Promotes Cellular Immunity via DNA Sensor cGAS-STING-Dependent Induction of Type I Interferons

机译:疫苗佐剂壳聚糖通过DNA传感器cGAS-STING依赖型I型干扰素的诱导来促进细胞免疫。

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摘要

The cationic polysaccharide chitosan is an attractive candidate adjuvant capable of driving potent cell-mediated immunity, but the mechanism by which it acts is not clear. We show that chitosan promotes dendritic cell maturation by inducing type I interferons (IFNs) and enhances antigen-specific T helper 1 (Th1) responses in a type I IFN receptor-dependent manner. The induction of type I IFNs, IFN-stimulated genes and dendritic cell maturation by chitosan required the cytoplasmic DNA sensor cGAS and STING, implicating this pathway in dendritic cell activation. Additionally, this process was dependent on mitochondrial reactive oxygen species and the presence of cytoplasmic DNA. Chitosan-mediated enhancement of antigen specific Th1 and immunoglobulin G2c responses following vaccination was dependent on both cGAS and STING. These findings demonstrate that a cationic polymer can engage the STING-cGAS pathway to trigger innate and adaptive immune responses.
机译:阳离子多糖壳聚糖是一种引人注目的候选佐剂,能够驱动有效的细胞介导的免疫力,但其作用机理尚不清楚。我们显示壳聚糖通过诱导I型干扰素(IFN)促进树突状细胞成熟,并以I型IFN受体依赖性方式增强抗原特异性T辅助1(Th1)反应。壳聚糖诱导I型干扰素,干扰素刺激的基因和树突状细胞成熟需要细胞质DNA传感器cGAS和STING,这与树突状细胞活化有关。另外,该过程取决于线粒体活性氧种类和细胞质DNA的存在。疫苗接种后,壳聚糖介导的抗原特异性Th1和免疫球蛋白G2c反应的增强取决于cGAS和STING。这些发现表明,阳离子聚合物可以参与STING-cGAS途径,以触发先天性和适应性免疫反应。

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