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CD4+ CD25+ Regulatory T Cells Control T Helper Cell Type 1 Responses to Foreign Antigens Induced by Mature Dendritic Cells In Vivo

机译:CD4 + CD25 +调节性T细胞控制T辅助细胞1型对成熟树突状细胞体外诱导的外源抗原的反应。

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摘要

Recent evidence suggests that in addition to their well known stimulatory properties, dendritic cells (DCs) may play a major role in peripheral tolerance. It is still unclear whether a distinct subtype or activation status of DC exists that promotes the differentiation of suppressor rather than effector T cells from naive precursors. In this work, we tested whether the naturally occurring CD4+ CD25+ regulatory T cells (Treg) may control immune responses induced by DCs in vivo. We characterized the immune response induced by adoptive transfer of antigen-pulsed mature DCs into mice depleted or not of CD25+ cells. We found that the development of major histocompatibility complex class I and II–restricted interferon γ–producing cells was consistently enhanced in the absence of Treg. By contrast, T helper cell (Th)2 priming was down-regulated in the same conditions. This regulation was independent of interleukin 10 production by DCs. Of note, splenic DCs incubated in vitro with Toll-like receptor ligands (lipopolysaccharide or CpG) activated immune responses that remained sensitive to Treg function. Our data further show that mature DCs induced higher cytotoxic activity in CD25-depleted recipients as compared with untreated hosts. We conclude that Treg naturally exert a negative feedback mechanism on Th1-type responses induced by mature DCs in vivo.
机译:最近的证据表明,除了其众所周知的刺激特性外,树突状细胞(DC)可能在外周耐受中起主要作用。尚不清楚是否存在DC的独特亚型或激活状态,其促进抑制性T细胞而不是效应T细胞与幼稚前体的分化。在这项工作中,我们测试了天然存在的CD4 + CD25 +调节性T细胞(Treg)是否可以控制体内DC诱导的免疫反应。我们表征了通过抗原脉冲成熟DC的过继转移进入CD25 +细胞是否耗尽的小鼠的免疫应答。我们发现,在没有Treg的情况下,主要的组织相容性复杂的I类和II类限制性干扰素γ产生细胞的发育一直得到增强。相比之下,T辅助细胞(Th)2引发在相同条件下被下调。该调节独立于DC产生的白介素10。值得注意的是,脾脏DC与Toll样受体配体(脂多糖或CpG)在体外孵育后激活了对Treg功能仍然敏感的免疫应答。我们的数据进一步表明,与未处理的宿主相比,成熟的DC在CD25耗尽的受体中诱导更高的细胞毒性活性。我们得出的结论是,Treg自然对体内成熟DC诱导的Th1型应答产生负反馈机制。

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