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本文引用的文献

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Pillars Article: Control of Regulatory T Cell Development by the Transcription Factor Foxp3. Science 2003. 299: 1057-1061.支柱文章:转录因子Foxp3对调节性T细胞发育的控制。《科学》2003年。299卷:1057 - 1061页。
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Role of LAG-3 in regulatory T cells.淋巴细胞活化基因3(LAG-3)在调节性T细胞中的作用。
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Engagement of glucocorticoid-induced TNFR family-related receptor on effector T cells by its ligand mediates resistance to suppression by CD4+CD25+ T cells.糖皮质激素诱导的TNFR家族相关受体在效应T细胞上被其配体激活,介导对CD4+CD25+ T细胞抑制作用的抵抗。
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Crucial role of FOXP3 in the development and function of human CD25+CD4+ regulatory T cells.FOXP3在人类CD25 + CD4 +调节性T细胞的发育和功能中的关键作用。
Int Immunol. 2004 Nov;16(11):1643-56. doi: 10.1093/intimm/dxh165. Epub 2004 Oct 4.
5
Recognition of the peripheral self by naturally arising CD25+ CD4+ T cell receptors.天然产生的CD25 + CD4 + T细胞受体对外周自身的识别。
Immunity. 2004 Aug;21(2):267-77. doi: 10.1016/j.immuni.2004.07.009.
6
Interleukin-2 is essential for CD4+CD25+ regulatory T cell function.白细胞介素-2对CD4+CD25+调节性T细胞功能至关重要。
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Suppressor T cells in human diseases.人类疾病中的抑制性T细胞。
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8
Compromised function of regulatory T cells in rheumatoid arthritis and reversal by anti-TNFalpha therapy.类风湿关节炎中调节性T细胞功能受损及抗TNFα治疗的逆转作用
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9
CD25(+)CD4(+) regulatory T cells from the peripheral blood of asymptomatic HIV-infected individuals regulate CD4(+) and CD8(+) HIV-specific T cell immune responses in vitro and are associated with favorable clinical markers of disease status.来自无症状HIV感染者外周血的CD25(+)CD4(+)调节性T细胞在体外调节CD4(+)和CD8(+)HIV特异性T细胞免疫反应,并与疾病状态的良好临床指标相关。
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10
Human immunodeficiency virus-driven expansion of CD4+CD25+ regulatory T cells, which suppress HIV-specific CD4 T-cell responses in HIV-infected patients.人类免疫缺陷病毒驱动的CD4+CD25+调节性T细胞扩增,其在HIV感染患者中抑制HIV特异性CD4 T细胞反应。
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CD4 + 调节性T细胞与免疫控制

CD4+ Tregs and immune control.

作者信息

Fehérvari Zoltán, Sakaguchi Shimon

机构信息

Department of Experimental Pathology, Institute for Frontier Medical Sciences, Kyoto University, Kyoto, Japan.

出版信息

J Clin Invest. 2004 Nov;114(9):1209-17. doi: 10.1172/JCI23395.

DOI:10.1172/JCI23395
PMID:15520849
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC524236/
Abstract

Recent years have seen Tregs become a popular subject of immunological research. Abundant experimental data have now confirmed that naturally occurring CD25+CD4+ Tregs in particular play a key role in the maintenance of self tolerance, with their dysfunction leading to severe or even fatal immunopathology. The sphere of influence of Tregs is now known to extend well beyond just the maintenance of immunological tolerance and to impinge on a host of clinically important areas from cancer to infectious diseases. The identification of specific molecular markers in both human and murine immune systems has enabled the unprecedented investigation of these cells and should prove key to ultimately unlocking their clinical potential.

摘要

近年来,调节性T细胞(Tregs)已成为免疫研究中的热门课题。大量实验数据现已证实,特别是自然产生的CD25 + CD4 + Tregs在维持自身耐受性方面发挥着关键作用,其功能障碍会导致严重甚至致命的免疫病理学。现在已知Tregs的影响范围远远超出免疫耐受的维持,并涉及从癌症到传染病等一系列临床上重要的领域。在人类和小鼠免疫系统中鉴定特定分子标志物,使得对这些细胞进行前所未有的研究成为可能,并且应该是最终释放其临床潜力的关键。