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本文引用的文献

1
Immune cell dysfunction and inflammation in end-stage renal disease.终末期肾病中的免疫细胞功能障碍和炎症。
Nat Rev Nephrol. 2013 May;9(5):255-65. doi: 10.1038/nrneph.2013.44. Epub 2013 Mar 19.
2
Uremia causes premature ageing of the T cell compartment in end-stage renal disease patients.尿毒症导致终末期肾病患者 T 细胞库过早衰老。
Immun Ageing. 2012 Sep 12;9(1):19. doi: 10.1186/1742-4933-9-19.
3
A killer on the road: circulating CD4(+)CD28null T cells as cardiovascular risk factor in ESRD patients.路上的杀手:循环 CD4(+)CD28null T 细胞作为 ESRD 患者的心血管风险因素。
J Nephrol. 2012 Mar-Apr;25(2):183-91. doi: 10.5301/jn.5000057.
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T cell exhaustion.T 细胞耗竭。
Nat Immunol. 2011 Jun;12(6):492-9. doi: 10.1038/ni.2035.
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Premature aging of circulating T cells in patients with end-stage renal disease.终末期肾病患者循环 T 细胞的过早衰老。
Kidney Int. 2011 Jul;80(2):208-17. doi: 10.1038/ki.2011.110. Epub 2011 Apr 27.
6
Old age and anti-cytomegalovirus immunity are associated with altered T-cell reconstitution in HIV-1-infected patients.衰老和抗巨细胞病毒免疫与 HIV-1 感染患者 T 细胞重建的改变有关。
AIDS. 2011 Sep 24;25(15):1813-22. doi: 10.1097/QAD.0b013e32834640e6.
7
Differential effects of age, cytomegalovirus-seropositivity and end-stage renal disease (ESRD) on circulating T lymphocyte subsets.年龄、巨细胞病毒血清阳性和终末期肾病 (ESRD) 对循环 T 淋巴细胞亚群的影响差异。
Immun Ageing. 2011 Jan 8;8(1):2. doi: 10.1186/1742-4933-8-2.
8
Epstein-Barr virus but not cytomegalovirus is associated with reduced vaccine antibody responses in Gambian infants.在冈比亚婴儿中,爱泼斯坦-巴尔病毒而非巨细胞病毒与疫苗抗体反应降低有关。
PLoS One. 2010 Nov 17;5(11):e14013. doi: 10.1371/journal.pone.0014013.
9
Estimating human age from T-cell DNA rearrangements.从T细胞DNA重排估计人类年龄。
Curr Biol. 2010 Nov 23;20(22):R970-1. doi: 10.1016/j.cub.2010.10.022.
10
HIV infection, inflammation, immunosenescence, and aging.HIV 感染、炎症、免疫衰老和衰老。
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巨细胞病毒在一定程度上导致了与尿毒症相关的 T 细胞亚群的过早免疫衰老。

Cytomegalovirus contributes partly to uraemia-associated premature immunological ageing of the T cell compartment.

机构信息

Department of Internal Medicine, Section Nephrology and Transplantation, Erasmus Medical Center, Rotterdam, the Netherlands.

出版信息

Clin Exp Immunol. 2013 Dec;174(3):424-32. doi: 10.1111/cei.12188.

DOI:10.1111/cei.12188
PMID:23962178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3826308/
Abstract

Cytomegalovirus (CMV) infection has been implicated in accelerated T cell ageing. End-stage renal disease (ESRD) patients have a severely immunologically aged T cell compartment but also a high prevalence of CMV infection. We investigated whether CMV infection contributes to T cell ageing in ESRD patients. We determined the thymic output by the T cell receptor excision circle (TREC) content and percentage of CD31+ naïve T cells. The proliferative history of the T cell compartment by determination of the relative telomere length (RTL) and the T cell differentiation status was determined by immunophenotyping. It appeared that CMV infection did not affect thymic output but reduced RTL of CD8+ T cells in ESRD patients. Moreover, increased T cell differentiation was observed with higher percentages of CD57+ and CD28null CD4+ and CD8+ memory T cells. These CD28null T cells had significantly shorter telomeres compared to CD28+ T cells. Therefore we concluded that CMV infection does not affect the decreased thymic output but increases T cell differentiation as observed in ESRD-related premature T cell ageing.

摘要

巨细胞病毒 (CMV) 感染与 T 细胞加速衰老有关。终末期肾病 (ESRD) 患者的 T 细胞免疫功能严重老化,但 CMV 感染也很普遍。我们研究了 CMV 感染是否会导致 ESRD 患者的 T 细胞衰老。我们通过检测 T 细胞受体切除环 (TREC) 含量和 CD31+幼稚 T 细胞的百分比来确定胸腺输出。通过相对端粒长度 (RTL) 和 T 细胞分化状态的测定来确定 T 细胞的增殖历史。结果表明,CMV 感染并未影响 ESRD 患者的胸腺输出,但降低了 CD8+T 细胞的 RTL。此外,观察到 CD57+和 CD28null CD4+和 CD8+记忆 T 细胞的百分比增加,表明 T 细胞分化增加。这些 CD28null T 细胞的端粒明显短于 CD28+T 细胞。因此,我们得出结论,CMV 感染不会影响 ESRD 相关的 T 细胞过早衰老中观察到的减少的胸腺输出,但会增加 T 细胞分化。