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Ageing promotes early T follicular helper cell differentiation by modulating expression of RBPJ

机译:衰老通过调节RBPJ的表达促进早期T滤泡辅助细胞分化

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摘要

Ageing profoundly changes our immune system and is thought to be a driving factor in the morbidity and mortality associated with infectious disease in older people. We have previously shown that the impaired immunity to vaccination that occurs in aged individuals is partly attributed to the effect of age on T follicular helper (Tfh) cell formation. In this study, we examined how age intrinsically affects Tfh cell formation in both mice and humans. We show increased formation of Tfh precursors (pre‐Tfh) but no associated increase in germinal centre (GC)‐Tfh cells in aged mice, suggesting age‐driven promotion of only early Tfh cell differentiation. Mechanistically, we show that ageing alters TCR signalling which drives expression of the Notch‐associated transcription factor, RBPJ. Genetic or chemical modulation of RBPJ or Notch rescues this age‐associated early Tfh cell differentiation, and increased intrinsic Notch activity recapitulates this phenomenon in younger mice. Our data offer mechanistic insight into the age‐induced changes in T‐cell activation that affects the differentiation and ultimately the function of effector T cells.
机译:老龄化深刻地改变了我们的免疫系统,并被认为是与老年人传染病相关的发病率和死亡率的驱动因素。我们以前表明,在老年人的疫苗接种中的免疫力受损部分归因于年龄对T卵泡辅助(TFH)细胞形成的效果。在这项研究中,我们检查了年龄的年龄如何影响小鼠和人类的TFH细胞形成。我们表明TFH前体(TFH)的形成增加,但在老年小鼠中没有发芽中心(GC)-TFH细胞的相关性,表明仅早期TFH细胞分化的年龄驱动促进。机械地,我们表明老化改变了推动凹口相关转录因子的表达的TCR信号传导。 RBPJ或Notch的遗传或化学调制拯救该年龄相关的早期TFH细胞分化,并且增加的内在缺口活性会促论在较年轻的小鼠中的这种现象。我们的数据提供了对T细胞活化的年龄诱导的变化的机械洞察,这些变化影响分化并最终效应T细胞的功能。

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