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Transferred antigen-specific T(H)17 but not T(H)1 cells induce crescentic glomerulonephritis in mice.转移抗原特异性 T(H)17 细胞而非 T(H)1 细胞可诱导小鼠新月体性肾小球肾炎。
Am J Pathol. 2011 Dec;179(6):2683-90. doi: 10.1016/j.ajpath.2011.08.017. Epub 2011 Oct 8.
2
The Th17-defining transcription factor RORγt promotes glomerulonephritis.转录因子 RORγt 促进了肾小球肾炎的发生。
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Th1 and Th17 cells induce proliferative glomerulonephritis.辅助性T细胞1(Th1)和辅助性T细胞17(Th17)可诱发增殖性肾小球肾炎。
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Chemokines play a critical role in the cross-regulation of Th1 and Th17 immune responses in murine crescentic glomerulonephritis.趋化因子在小鼠新月体性肾小球肾炎中 Th1 和 Th17 免疫反应的交叉调控中发挥着关键作用。
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TH1 and TH17 cells promote crescent formation in experimental autoimmune glomerulonephritis.TH1细胞和TH17细胞在实验性自身免疫性肾小球肾炎中促进新月体形成。
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Endogenous interleukin-10 regulates Th1 responses that induce crescentic glomerulonephritis.内源性白细胞介素-10调节诱导新月体性肾小球肾炎的Th1反应。
Kidney Int. 2000 Feb;57(2):518-25. doi: 10.1046/j.1523-1755.2000.00872.x.
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Interleukin-4 deficiency enhances Th1 responses and crescentic glomerulonephritis in mice.白细胞介素-4缺乏增强小鼠的Th1反应和新月体性肾小球肾炎。
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T-bet deficiency attenuates renal injury in experimental crescentic glomerulonephritis.T-bet缺陷减轻实验性新月体性肾小球肾炎中的肾损伤。
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Endogenous Tim-1 (Kim-1) promotes T-cell responses and cell-mediated injury in experimental crescentic glomerulonephritis.内源性 Tim-1(Kim-1)促进实验性新月体性肾小球肾炎中的 T 细胞反应和细胞介导的损伤。
Kidney Int. 2012 May;81(9):844-55. doi: 10.1038/ki.2011.424. Epub 2011 Dec 28.

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CXCR3+ Regulatory T Cells Control TH1 Responses in Crescentic GN.CXCR3+调节性T细胞控制新月体性肾小球肾炎中的TH1反应。
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Local IL-17 Production Exerts a Protective Role in Murine Experimental Glomerulonephritis.局部白细胞介素-17的产生在小鼠实验性肾小球肾炎中发挥保护作用。
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本文引用的文献

1
The transient nature of the Th17 phenotype.Th17 表型的瞬时性。
Eur J Immunol. 2010 Dec;40(12):3312-6. doi: 10.1002/eji.201041145.
2
CCR6 recruits regulatory T cells and Th17 cells to the kidney in glomerulonephritis.CCR6 将调节性 T 细胞和 Th17 细胞募集到肾小球肾炎的肾脏中。
J Am Soc Nephrol. 2010 Jun;21(6):974-85. doi: 10.1681/ASN.2009070741. Epub 2010 Mar 18.
3
Th1 and Th17 cells induce proliferative glomerulonephritis.辅助性T细胞1(Th1)和辅助性T细胞17(Th17)可诱发增殖性肾小球肾炎。
J Am Soc Nephrol. 2009 Dec;20(12):2518-24. doi: 10.1681/ASN.2009030337. Epub 2009 Oct 9.
4
The IL-23/Th17 axis contributes to renal injury in experimental glomerulonephritis.白细胞介素-23/辅助性T细胞17轴在实验性肾小球肾炎中导致肾损伤。
J Am Soc Nephrol. 2009 May;20(5):969-79. doi: 10.1681/ASN.2008050556. Epub 2009 Apr 1.
5
IL-17 and Th17 Cells.白细胞介素-17与辅助性T细胞17
Annu Rev Immunol. 2009;27:485-517. doi: 10.1146/annurev.immunol.021908.132710.
6
A rush to judgment on Th17.对辅助性T细胞17(Th17)的仓促评判。
J Exp Med. 2008 Jul 7;205(7):1517-22. doi: 10.1084/jem.20072066.
7
IL-12- and IL-23-modulated T cells induce distinct types of EAE based on histology, CNS chemokine profile, and response to cytokine inhibition.基于组织学、中枢神经系统趋化因子谱以及对细胞因子抑制的反应,白细胞介素-12和白细胞介素-23调节的T细胞可诱导不同类型的实验性自身免疫性脑脊髓炎。
J Exp Med. 2008 Jul 7;205(7):1535-41. doi: 10.1084/jem.20080159. Epub 2008 Jun 23.
8
Either a Th17 or a Th1 effector response can drive autoimmunity: conditions of disease induction affect dominant effector category.Th17或Th1效应反应均可引发自身免疫:疾病诱导条件会影响主要效应类别。
J Exp Med. 2008 Apr 14;205(4):799-810. doi: 10.1084/jem.20071258. Epub 2008 Apr 7.
9
Th17: the third member of the effector T cell trilogy.辅助性T细胞17:效应T细胞三部曲的第三个成员。
Curr Opin Immunol. 2007 Dec;19(6):652-7. doi: 10.1016/j.coi.2007.07.020. Epub 2007 Sep 4.
10
Blockade of chronic graft-versus-host disease by alloantigen-induced CD4+CD25+Foxp3+ regulatory T cells in nonlymphopenic hosts.非淋巴细胞减少宿主中同种异体抗原诱导的CD4 + CD25 + Foxp3 +调节性T细胞对慢性移植物抗宿主病的阻断作用。
J Leukoc Biol. 2007 Nov;82(5):1053-61. doi: 10.1189/jlb.0407227. Epub 2007 Aug 7.

转移抗原特异性 T(H)17 细胞而非 T(H)1 细胞可诱导小鼠新月体性肾小球肾炎。

Transferred antigen-specific T(H)17 but not T(H)1 cells induce crescentic glomerulonephritis in mice.

机构信息

MRC Centre for Transplantation, King's College London School of Medicine, London, England.

出版信息

Am J Pathol. 2011 Dec;179(6):2683-90. doi: 10.1016/j.ajpath.2011.08.017. Epub 2011 Oct 8.

DOI:10.1016/j.ajpath.2011.08.017
PMID:21983633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3260861/
Abstract

To explore the role of antigen-specific CD4(+) T cells in glomerulonephritis, we administered ovalbumin 323-339 peptide conjugated to glomerular-binding polyclonal antibody and induced disease in RAG1(-/-) mice with CD4(+) T cells from OT2 × RAG1(-/-) mice. These OT2 × RAG1(-/-) mice have a transgenic T-cell receptor specific for this peptide. When CD4(+) T cells were primed in vivo, crescentic glomerulonephritis developed after 21 days in mice given peptide-conjugated glomerular-binding antibody but not unconjugated antibody control. We then investigated the relative roles of T(H)1 and T(H)17 cells, using Fab(2) fragments of glomerular-binding antibody to exclude a role for antibody in this model. T cells from OT2 × RAG1(-/-) mice were polarized in vitro, and T(H)1 or T(H)17 cell lines were injected into mice that were also given peptide-conjugated Fab(2) or unconjugated Fab(2) control, giving four experimental groups. After 21 days crescentic glomerulonephritis was seen in mice receiving T(H)17 cells and peptide-conjugated Fab(2) but in none of the other three groups. These results suggest that T(H)17 but not T(H)1 cells can induce crescentic glomerulonephritis.

摘要

为了探索抗原特异性 CD4(+)T 细胞在肾小球肾炎中的作用,我们用与肾小球结合的多克隆抗体偶联的卵清蛋白 323-339 肽处理 RAG1(-/-)小鼠,并向其输注 OT2×RAG1(-/-)小鼠的 CD4(+)T 细胞以诱导疾病。这些 OT2×RAG1(-/-)小鼠具有针对该肽的转基因 T 细胞受体。当 CD4(+)T 细胞在体内被激活时,给予肽偶联的肾小球结合抗体而非未偶联抗体对照的小鼠在 21 天后会发展为新月体性肾小球肾炎。然后,我们使用肾小球结合抗体的 Fab(2)片段来研究 T(H)1 和 T(H)17 细胞的相对作用,以排除该模型中抗体的作用。从 OT2×RAG1(-/-)小鼠中体外极化 T 细胞,并将 T(H)1 或 T(H)17 细胞系注入也给予肽偶联 Fab(2)或未偶联 Fab(2)对照的小鼠中,共分为四个实验组。21 天后,接受 T(H)17 细胞和肽偶联 Fab(2)的小鼠出现新月体性肾小球肾炎,但在其他三组中均未出现。这些结果表明,T(H)17 而非 T(H)1 细胞可诱导新月体性肾小球肾炎。