Treatment with anti-interleukin 23 antibody ameliorates disease in lupus-prone mice.

Treatment with anti-interleukin 23 antibody ameliorates disease in lupus-prone mice.
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DOI:
10.1155/2013/861028
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发表时间:
2013
影响因子:
--
通讯作者:
Tsokos GC
Tsokos GC
中科院分区:
生物学3区
文献类型:
--
作者:
Kyttaris VC;Kampagianni O;Tsokos GC

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IL-23受体表达IL-17产生的T细胞在小鼠狼疮的发生发展中起重要作用。IL-23抑制在改善狼疮性肾炎中的作用尚不清楚。我们假设抑制IL-23将改善狼疮易感小鼠的肾炎。为此,我们用鼠抗IL-23p19抗体治疗MRL/LPR狼疮易感小鼠6周,结果是在不影响抗dsDNA抗体产生的情况下延缓了肾炎的发生。治疗效果因产生鼠抗鼠免疫球蛋白抗体而受阻。抑制IL-23对小鼠狼疮的改善加强了在系统性红斑狼疮患者中靶向IL-23的理由。
Interleukin 23 receptor expressing IL-17 producing T cells have been shown to be important in the development of murine lupus. The usefulness of IL-23 inhibition in ameliorating lupus nephritis is unknown. We hypothesized that inhibition of IL-23 will ameliorate nephritis in lupus-prone mice. To this end, we treated MRL/lpr lupus-prone mice for 6 weeks with a rat anti-IL-23p19 antibody, which resulted in delaying the onset of nephritis without affecting the production of anti-dsDNA antibodies. The effect of the treatment was hampered by the production of murine anti-rat IgG antibodies. The amelioration of murine lupus by IL-23 inhibition strengthens the rationale for targeting IL-23 in patients with systemic lupus erythematosus.
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