首页> 外文期刊>Clinical and Experimental Immunology: An Official Journal of the British Society for Immunology >Interleukin (IL)-39 [IL-23p19/Epstein-Barr virus-induced 3 (Ebi3)] induces differentiation/expansion of neutrophils in lupus-prone mice
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Interleukin (IL)-39 [IL-23p19/Epstein-Barr virus-induced 3 (Ebi3)] induces differentiation/expansion of neutrophils in lupus-prone mice

机译:白细胞介素(IL)-39 [IL-23p19 / Epstein-Barr病毒诱导的3(Ebi3)]诱发易患狼疮的小鼠中性粒细胞的分化/扩增

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Interleukin (IL)-12 family cytokines play critical roles in autoimmune diseases. Our previous study has shown that IL-23p19 and Epstein-Barr virus-induced 3 (Ebi3) form a new IL-12 family heterodimer, IL-23p19/Ebi3, termed IL-39, and knock-down of p19 or Ebi3 reduced diseases by transferred GL7(+) B cells in lupus-prone mice. In the present study, we explore further the possible effect of IL-39 on murine lupus. We found that IL-39 in vitro and in vivo induces differentiation and/or expansion of neutrophils. GL7(+) B cells up-regulated neutrophils by secreting IL-39, whereas IL-39-deficient GL7(+) B cells lost the capacity to up-regulate neutrophils in lupus-prone mice and homozygous CD19(cre) (CD19-deficient) mice. Finally, we found that IL-39-induced neutrophils had a positive feedback on IL-39 expression in activated B cells by secreting B cell activation factor (BAFF). Taken together, our results suggest that IL-39 induces differentiation and/or expansion of neutrophils in lupus-prone mice.
机译:白介素(IL)-12家族细胞因子在自身免疫性疾病中起关键作用。我们以前的研究表明,IL-23p19和爱泼斯坦-巴尔病毒诱导的3(Ebi3)形成了新的IL-12家族异二聚体IL-23p19 / Ebi3,称为IL-39,并敲低了p19或Ebi3减少的疾病易患狼疮的小鼠体内转移的GL7(+)B细胞。在本研究中,我们进一步探讨了IL-39对小鼠狼疮的可能作用。我们发现IL-39在体外和体内诱导中性粒细胞的分化和/或扩增。 GL7(+)B细胞通过分泌IL-39上调中性粒细胞,而IL-39缺陷的GL7(+)B细胞失去了在易患狼疮的小鼠和纯合CD19(cre)(CD19-缺陷)小鼠。最后,我们发现IL-39诱导的中性粒细胞通过分泌B细胞活化因子(BAFF)对活化B细胞中IL-39表达具有正反馈。两者合计,我们的结果表明,IL-39在易患狼疮的小鼠中诱导中性粒细胞的分化和/或扩增。

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