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造血干细胞移植后FoxP3+CD4+25+调节性T细胞的诱导:骨髓来源促进细胞的作用

Induction of FoxP3+CD4+25+ regulatory T cells following hemopoietic stem cell transplantation: role of bone marrow-derived facilitating cells.

作者信息

Taylor Kendra N, Shinde-Patil Vivek R, Cohick Evan, Colson Yolonda L

机构信息

Division of Thoracic Surgery, Department of Surgery Brigham and Women's Hospital, Boston, MA 02115, USA.

出版信息

J Immunol. 2007 Aug 15;179(4):2153-62. doi: 10.4049/jimmunol.179.4.2153.

Abstract

The establishment of donor cell lineages following allogeneic bone marrow transplantation is frequently associated with the development of graft-vs-host disease (GVHD). The identification of cell populations that are capable of supporting allogeneic stem cell (SC) engraftment and the induction of tolerance without inducing GVHD could expand the use of this therapy. CD8(+)TCR(-) facilitating cells (FC) have been shown to promote allogeneic SC engraftment with resulting transplantation tolerance across complete MHC barriers without inducing GVHD. Although donor reconstitution in SC plus FC recipients is associated with the induction of regulatory T cell-associated factors, it is not known whether an induction of regulatory T cells and subsequent tolerance is a direct effect of the FC. The current study demonstrates that 1) SC plus FC transplantation results in the induction of donor CD4(+)25(+) regulatory T cells and that FC are present in the spleen of recipients before the induction of these cells, 2) activation of FC with CpG-oligodeoxynucleotide promotes CD4(+)25(-) T cell differentiation into CD4(+)25(+) regulatory T cells in vitro, as demonstrated by cytokine and forkhead/winged helix transcription factor (FoxP3) gene and protein expression, and 3) direct contact between FC and CD4(+)25(-) T cells is required for FoxP3(+)CD4(+)25(+) regulatory T cell induction and is dependent on CD86 expression on FC. This is the first report to demonstrate a mechanism for FC in the induction of regulatory T cells following allogeneic SC plus FC transplantation. The transplantation of donor FC may provide an alternative approach to permit clinical SC engraftment and induction of transplantation tolerance in the future.

摘要

同种异体骨髓移植后供体细胞谱系的建立常常与移植物抗宿主病(GVHD)的发生相关。鉴定能够支持同种异体干细胞(SC)植入并诱导耐受而不诱发GVHD的细胞群体,可能会扩大这种治疗方法的应用。已表明CD8(+)TCR(-)促进细胞(FC)可促进同种异体SC植入,并在完全的主要组织相容性复合体(MHC)屏障下产生移植耐受而不诱发GVHD。尽管在SC加FC受体中供体的重建与调节性T细胞相关因子的诱导有关,但尚不清楚调节性T细胞的诱导及随后的耐受是否是FC的直接作用。当前研究表明:1)SC加FC移植可导致供体CD4(+)25(+)调节性T细胞的诱导,并且在这些细胞诱导之前,FC存在于受体的脾脏中;2)用CpG-寡脱氧核苷酸激活FC可在体外促进CD4(+)25(-)T细胞分化为CD4(+)25(+)调节性T细胞,这通过细胞因子、叉头/翼状螺旋转录因子(FoxP3)基因及蛋白表达得以证明;3)FoxP3(+)CD4(+)25(+)调节性T细胞的诱导需要FC与CD4(+)25(-)T细胞直接接触,并且依赖于FC上CD86的表达。这是第一份证明FC在同种异体SC加FC移植后诱导调节性T细胞中的机制的报告。供体FC的移植可能为未来实现临床SC植入及诱导移植耐受提供一种替代方法。

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