...
首页> 外文期刊>European journal of pediatrics >Age-dependent changes in peripheral blood dendritic cell subsets in normal children and children with specific polysaccharide antibody deficiency (SPAD).
【24h】

Age-dependent changes in peripheral blood dendritic cell subsets in normal children and children with specific polysaccharide antibody deficiency (SPAD).

机译:正常儿童和特定多糖抗体缺乏症(SPAD)儿童的外周血树突状细胞亚群的年龄依赖性变化。

获取原文
获取原文并翻译 | 示例
           

摘要

Myeloid and plasmacytoid dendritic cells (MDC/PDC) play crucial roles in bridging adaptive and innate immunity by affecting development of both cellular and humoral immunity. The immune system evolves after birth as reflected in dynamic changes in numbers and functions of various immune cells with age. However, age-associated changes in DC subsets in children have not been elucidated despite the fact that such normative data are crucial for evaluating alternations of DC subsets in various pediatric diseases. This study addressed age-associated changes in DC subsets and CD40/86 expression on PDC (markers of maturation/activation) in 50 healthy children in comparison with 25 children with specific polysaccharide antibody deficiency (SPAD). Our results revealed age-dependent decrease of PDC numbers (p < 0.0001), although there was no age-associated changes in CD40/CD86 expression. MDC1/MDC2 numbers did not reveal such linear age-dependent changes and MDC1/PDC ratio reached around 2 as typically seen in young adults after 10 years of age. In contrast, SPAD patients did not reveal such age-associated changes and showed decreased fluorescence intensity of CD86 in PDC cells. These results indicate lineage specific, age-dependent changes in DC subsets in normal children and possible altered development of these cells in SPAD children, emphasizing the importance of age-appropriate controls.
机译:髓样和浆细胞样树突状细胞(MDC / PDC)通过影响细胞和体液免疫的发展,在桥接适应性免疫和先天性免疫中发挥关键作用。免疫系统在出生后就会进化,这反映出各种免疫细胞的数量和功能随着年龄的增长而动态变化。然而,尽管这样的规范化数据对于评估各种儿科疾病中DC子集的替代至关重要,但仍未阐明儿童中DC子集的年龄相关变化。这项研究针对的是50名健康儿童与25名患有特定多糖抗体缺乏症(SPAD)的儿童相比,DC子集和PDC上CD40 / 86表达(成熟/激活的标志)与年龄相关的变化。我们的结果显示,尽管CD40 / CD86表达没有与年龄相关的变化,但PDC数目随年龄的下降而下降(p <0.0001)。 MDC1 / MDC2的数字并未显示出这种线性的年龄依赖性变化,MDC1 / PDC的比例达到了大约2,这在10岁后的年轻成年人中通常可见。相比之下,SPAD患者未显示出与年龄相关的变化,并且显示PDC细胞中CD86的荧光强度降低。这些结果表明正常儿童DC子集中特定于世系的,年龄相关的变化,以及SPAD儿童中这些细胞的发育可能发生改变,强调了适合年龄的对照的重要性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号