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首页> 外文期刊>Journal of molecular cell biology >Polyclonal CD4+Foxp3+ Treg cells induce TGFβ-dependent tolerogenic dendritic cells that suppress the murine lupus-like syndrome
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Polyclonal CD4+Foxp3+ Treg cells induce TGFβ-dependent tolerogenic dendritic cells that suppress the murine lupus-like syndrome

机译:多克隆CD4 + Foxp3 + Treg细胞诱导TGFβ依赖性耐受性树突状细胞,抑制鼠类狼疮样综合征

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Interplay between Foxp3+ regulatory T cells (Treg) and dendritic cells (DCs) maintains immunologic tolerance, but the effects of each cell on the other are not well understood. We report that polyclonal CD4+Foxp3+ Treg cells induced ex vivo with transforming growth factor beta (TGFβ) (iTreg) suppress a lupus-like chronic graft-versus-host disease by preventing the expansion of immunogenic DCs and inducing protective DCs that generate additional recipient CD4+Foxp3+ cells. The protective effects of the transferred iTreg cells required both interleukin (IL)-10 and TGFβ, but the tolerogenic effects of the iTreg on DCs, and the immunosuppressive effects of these DCs were exclusively TGFβ-dependent. The iTreg were unable to tolerize Tgfbr2-deficient DCs. These results support the essential role of DCs in ‘infectious tolerance’ and emphasize the central role of TGFβ in protective iTreg/DC interactions in vivo.
机译:Foxp3 +调节性T细胞(Treg)和树突状细胞(DCs)之间的相互作用维持了免疫耐受性,但每个细胞对另一个的影响尚不十分清楚。我们报告说,多克隆CD4 + Foxp3 + Treg细胞通过转化生长因子β(TGFβ)(iTreg)离体诱导,通过阻止免疫原性DC的扩展并诱导产生额外受体的保护性DC抑制了狼疮样慢性移植物抗宿主病。 CD4 + Foxp3 +细胞。转移的iTreg细胞的保护作用需要白介素(IL)-10和TGFβ,但是iTreg对DC的致耐受作用以及这些DC的免疫抑制作用完全是TGFβ依赖性的。 iTreg无法耐受Tgfbr2缺失的DC。这些结果支持了DC在“感染耐受”中的重要作用,并强调了TGFβ在体内iTreg / DC保护性相互作用中的核心作用。

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