首页> 外文期刊>Birth defects research, Part B. Developmental and reproductive toxicology >The effects of interleukin-6 signal blockade on immune system, reproductive and skeletal development in juvenile mice
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The effects of interleukin-6 signal blockade on immune system, reproductive and skeletal development in juvenile mice

机译:白细胞介素6信号阻断对幼年小鼠免疫系统,生殖和骨骼发育的影响

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摘要

Interleukin-6 (IL-6) is involved in the pathogenesis of multiple disorders, including juvenile autoimmune diseases. IL-6 participates in a broad spectrum of physiological events, and the IL-6 receptor (IL-6R) is widely distributed across multiple organs. The interrelationship of development phases in juveniles together with organs involved in IL-6 signaling called for evaluations of anti-IL-6R antibody induced effects in a juvenile mouse model to assess the safety of such an approach in human juvenile arthritis. Here we show that naive mice in which IL-6 signals have been transiently blocked during the juvenile period develop normally. The fatal immunogenic reactions recorded earlier by repeated administration of the chosen rat anti-mouse IL-6R antibody, MR16-1, to mice were avoided successfully by application of a high loading dose followed by lower maintenance doses, with the support of modeling data. The high loading-dose regimen enabled us to conduct assessments without any major interference due to immunogenicity. Transient and complete inhibition of IL-6 signals from postnatal days 22 to 79 in mice exhibited no biologically important changes in sexual maturation or development of immune and skeletal systems. Although tendencies toward reductions of peripheral blood T-cell counts were observed, normal levels of antigen-specific IgG/IgM antibody productions indicating sufficient immunological functions were confirmed. Our results demonstrate that blockage of IL-6R by the neutralizing antibody does not affect juvenile development. This may be in part due to the generation or existence of compensatory pathways in the whole body system.
机译:白介素-6(IL-6)参与多种疾病的发病机制,包括青少年自身免疫性疾病。 IL-6参与广泛的生理事件,并且IL-6受体(IL-6R)广泛分布于多个器官。幼体发育阶段与参与IL-6信号传导的器官之间的相互关系要求评估在幼年小鼠模型中抗IL-6R抗体诱导的作用,以评估这种方法在人类幼年关节炎中的安全性。在这里,我们显示了其中IL-6信号在幼年时期被短暂阻断的幼稚小鼠正常发育。通过在模型数据的支持下,先施加高负荷剂量然后降低维持剂量,可以成功避免先前通过反复向小鼠反复施用所选大鼠抗小鼠IL-6R抗体MR16-1而记录的致命免疫原性反应。高负荷剂量方案使我们能够进行评估,而不会因免疫原性而受到任何重大干扰。从小鼠出生后第22天到第79天对IL-6信号的瞬时和完全抑制在性成熟或免疫系统和骨骼系统发育方面没有生物学上的重要变化。尽管观察到外周血T细胞计数降低的趋势,但是证实了表明足够的免疫功能的抗原特异性IgG / IgM抗体产生的正常水平。我们的结果表明,中和抗体对IL-6R的阻滞不会影响青少年的发育。这可能部分是由于整个人体系统中补偿路径的产生或存在。

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