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2
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Reconstitution of FOXP3+ regulatory T cells (Tregs) after CD25-depleted allotransplantation in elderly patients and association with acute graft-versus-host disease.老年患者CD25去除后同种异体移植中FOXP3 +调节性T细胞(Tregs)的重建及其与急性移植物抗宿主病的关系
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[The role of CD4+ CD25+ T cell and FOXP3 in hsot acute graft rejection].[CD4+CD25+T细胞及FOXP3在同种异体肝移植急性排斥反应中的作用] (注:原文中“hsot”可能有误,推测为“同种异体肝移植”“homologous liver transplantation”的相关错误表述,这里根据正确理解翻译)
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Immune Reconstitution after Haploidentical Hematopoietic Stem Cell Transplantation with Different Non-T-Cell Depletion Protocols.采用不同非T细胞去除方案的单倍体造血干细胞移植后的免疫重建
MedComm (2020). 2025 May 19;6(6):e70206. doi: 10.1002/mco2.70206. eCollection 2025 Jun.
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The impact of regulatory T cells on the graft-versus-leukemia effect.调节性 T 细胞对移植物抗白血病效应的影响。
Front Immunol. 2024 Apr 22;15:1339318. doi: 10.3389/fimmu.2024.1339318. eCollection 2024.
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Inflammatory CD4/CD8 double-positive human T cells arise from reactive CD8 T cells and are sufficient to mediate GVHD pathology.炎性 CD4/CD8 双阳性人类 T 细胞源自反应性 CD8 T 细胞,足以介导移植物抗宿主病病理学。
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本文引用的文献

1
The fate of human Treg cells.人类调节性T细胞的命运。
Immunity. 2009 Jun 19;30(6):763-5. doi: 10.1016/j.immuni.2009.06.006.
2
Functional delineation and differentiation dynamics of human CD4+ T cells expressing the FoxP3 transcription factor.表达FoxP3转录因子的人CD4+ T细胞的功能划分与分化动力学
Immunity. 2009 Jun 19;30(6):899-911. doi: 10.1016/j.immuni.2009.03.019. Epub 2009 May 21.
3
Patients suffering from acute graft-versus-host disease after bone-marrow transplantation have functional CD4+CD25hiFoxp3+ regulatory T cells.骨髓移植后患有急性移植物抗宿主病的患者具有功能性CD4+CD25hiFoxp3+调节性T细胞。
Clin Immunol. 2008 Nov;129(2):241-8. doi: 10.1016/j.clim.2008.07.019. Epub 2008 Aug 29.
4
Extracorporeal photopheresis reverses experimental graft-versus-host disease through regulatory T cells.体外光分离置换法通过调节性T细胞逆转实验性移植物抗宿主病。
Blood. 2008 Aug 15;112(4):1515-21. doi: 10.1182/blood-2007-11-125542. Epub 2008 Apr 14.
5
Differential impact of mammalian target of rapamycin inhibition on CD4+CD25+Foxp3+ regulatory T cells compared with conventional CD4+ T cells.与传统CD4+ T细胞相比,雷帕霉素哺乳动物靶点抑制对CD4+CD25+Foxp3+调节性T细胞的不同影响。
Blood. 2008 Jan 1;111(1):453-62. doi: 10.1182/blood-2007-06-094482. Epub 2007 Oct 29.
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Role of regulatory T cells and FOXP3 in human diseases.调节性T细胞和FOXP3在人类疾病中的作用。
J Allergy Clin Immunol. 2007 Aug;120(2):227-35; quiz 236-7. doi: 10.1016/j.jaci.2007.06.023.
7
Induction of FOXP3 expression in naive human CD4+FOXP3 T cells by T-cell receptor stimulation is transforming growth factor-beta dependent but does not confer a regulatory phenotype.通过T细胞受体刺激在未成熟人CD4⁺FOXP3⁺ T细胞中诱导FOXP3表达是转化生长因子-β依赖性的,但不会赋予调节性表型。
Blood. 2007 Oct 15;110(8):2983-90. doi: 10.1182/blood-2007-06-094656. Epub 2007 Jul 20.
8
Reconstitution of FOXP3+ regulatory T cells (Tregs) after CD25-depleted allotransplantation in elderly patients and association with acute graft-versus-host disease.老年患者CD25去除后同种异体移植中FOXP3 +调节性T细胞(Tregs)的重建及其与急性移植物抗宿主病的关系
Blood. 2007 Sep 1;110(5):1689-97. doi: 10.1182/blood-2007-03-079160. Epub 2007 May 3.
9
Regulatory T-cells in the graft and the risk of acute graft-versus-host disease after allogeneic stem cell transplantation.移植物中的调节性T细胞与异基因干细胞移植后急性移植物抗宿主病的风险
Transplantation. 2007 Apr 27;83(8):1107-13. doi: 10.1097/01.tp.0000260140.04815.77.
10
Rapamycin, not cyclosporine, permits thymic generation and peripheral preservation of CD4+ CD25+ FoxP3+ T cells.雷帕霉素而非环孢素能使CD4+ CD25+ FoxP3+ T细胞在胸腺中生成并在外周得以保存。
Bone Marrow Transplant. 2007 May;39(9):537-45. doi: 10.1038/sj.bmt.1705628. Epub 2007 Mar 12.

CD4(+)CD25(hi)FOXP3(+) 调节性 T 细胞的频率作为急性移植物抗宿主病的生物标志物具有诊断和预后价值。

Frequency of CD4(+)CD25(hi)FOXP3(+) regulatory T cells has diagnostic and prognostic value as a biomarker for acute graft-versus-host-disease.

机构信息

Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA.

出版信息

Biol Blood Marrow Transplant. 2010 Jul;16(7):907-14. doi: 10.1016/j.bbmt.2010.02.026. Epub 2010 Mar 17.

DOI:10.1016/j.bbmt.2010.02.026
PMID:20302964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2916071/
Abstract

The relationship between regulatory T cells (Tregs) and acute graft-versus-host disease (aGVHD) in clinical allogeneic bone marrow transplantation (BMT) recipients is not well established. We conducted a prospective analysis of peripheral blood Tregs as determined by the frequency of CD4(+)CD25(hi)FOXP3(+) lymphocytes in 215 BMT patients. Autologous BMT patients (N = 90) and allogeneic BMT patients without GVHD (N = 65) had similar Treg frequencies, whereas allogeneic patients with GVHD (N = 60) had Treg frequencies that were 40% less than those without GVHD. Treg frequencies decreased linearly with increasing grades of GVHD at onset, and correlated with eventual maximum grade of GVHD (P < .001). In addition, frequency of Tregs at onset of GVHD predicted the response to GVHD treatment (P = .003). Patients with Treg frequencies less than the median had higher nonrelapse mortality (NRM) than patients with Tregs greater than the median, but experienced equivalent relapse mortality, resulting in an inferior survival at 2 years (38% versus 63%, P = .03). Treg frequency may therefore have important prognostic value as a biomarker of aGVHD.

摘要

在接受临床同种异体骨髓移植 (BMT) 的患者中,调节性 T 细胞 (Tregs) 与急性移植物抗宿主病 (aGVHD) 之间的关系尚未明确。我们对 215 名 BMT 患者的外周血 Tregs 进行了前瞻性分析,通过 CD4(+)CD25(hi)FOXP3(+)淋巴细胞的频率来确定 Tregs。自体 BMT 患者 (N = 90) 和无 GVHD 的同种异体 BMT 患者 (N = 65) 的 Treg 频率相似,而有 GVHD 的同种异体患者 (N = 60) 的 Treg 频率比无 GVHD 的患者低 40%。Treg 频率随 GVHD 发病时的严重程度呈线性下降,与最终 GVHD 的严重程度相关 (P <.001)。此外,GVHD 发病时 Treg 的频率预测 GVHD 治疗的反应 (P =.003)。Treg 频率低于中位数的患者比 Treg 频率高于中位数的患者的非复发死亡率 (NRM) 更高,但经历了同等的复发死亡率,导致 2 年的生存情况较差 (38%对 63%,P =.03)。因此,Treg 频率可能作为 aGVHD 的生物标志物具有重要的预后价值。