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本文引用的文献

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Hallmarks of human "immunosenescence": adaptation or dysregulation?人类“免疫衰老”的特征:适应还是失调?
Immun Ageing. 2012 Jul 25;9(1):15. doi: 10.1186/1742-4933-9-15.
2
High cardiovascular risk in severely obese young children and adolescents.严重肥胖的婴幼儿存在较高心血管风险。
Arch Dis Child. 2012 Sep;97(9):818-21. doi: 10.1136/archdischild-2012-301877. Epub 2012 Jul 23.
3
Health-related quality of life in adolescents with or at risk for type 2 diabetes mellitus.青少年 2 型糖尿病患者或糖尿病风险者的健康相关生活质量。
J Pediatr. 2012 Jun;160(6):911-7. doi: 10.1016/j.jpeds.2011.11.026. Epub 2012 Jan 3.
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Inflammation and reactivation of latent herpesviruses in older adults.老年人潜伏疱疹病毒的炎症和激活。
Brain Behav Immun. 2012 Jul;26(5):739-46. doi: 10.1016/j.bbi.2011.11.007. Epub 2011 Dec 1.
5
Oxidant mechanisms in childhood obesity: the link between inflammation and oxidative stress.儿童肥胖中的氧化剂机制:炎症与氧化应激之间的联系。
Transl Res. 2011 Dec;158(6):369-84. doi: 10.1016/j.trsl.2011.08.004. Epub 2011 Sep 3.
6
Obesity is associated with impaired immune response to influenza vaccination in humans.肥胖与人类对流感疫苗接种的免疫反应受损有关。
Int J Obes (Lond). 2012 Aug;36(8):1072-7. doi: 10.1038/ijo.2011.208. Epub 2011 Oct 25.
7
Infection with cytomegalovirus but not herpes simplex virus induces the accumulation of late-differentiated CD4+ and CD8+ T-cells in humans.巨细胞病毒感染而非单纯疱疹病毒感染可诱导人类晚期分化的 CD4+和 CD8+T 细胞的积累。
J Gen Virol. 2011 Dec;92(Pt 12):2746-2756. doi: 10.1099/vir.0.036004-0. Epub 2011 Aug 3.
8
Aerobic fitness is associated with lower proportions of senescent blood T-cells in man.有氧运动能力与人类血液中衰老 T 细胞的比例较低有关。
Brain Behav Immun. 2011 Nov;25(8):1521-9. doi: 10.1016/j.bbi.2011.07.226. Epub 2011 Jul 19.
9
Association between HSV1 seropositivity and obesity: data from the National Health and Nutritional Examination Survey, 2007-2008.单纯疱疹病毒 1 型血清阳性与肥胖的相关性:来自 2007-2008 年全国健康和营养调查的数据。
PLoS One. 2011 May 11;6(5):e19092. doi: 10.1371/journal.pone.0019092.
10
A novel risk factor for a novel virus: obesity and 2009 pandemic influenza A (H1N1).肥胖是 2009 年甲型 H1N1 流感的一个新的危险因素。
Clin Infect Dis. 2011 Feb 1;52(3):301-12. doi: 10.1093/cid/ciq152. Epub 2011 Jan 4.

超重与儿童免疫衰老相关的 T 细胞分化有关。

Excess body mass is associated with T cell differentiation indicative of immune ageing in children.

机构信息

Laboratory of Integrated Physiology, Department of Health and Human Performance, University of Houston, Houston, TX, USA; Texas Obesity Research Center, University of Houston, Houston, TX, USA.

出版信息

Clin Exp Immunol. 2014 May;176(2):246-54. doi: 10.1111/cei.12267.

DOI:10.1111/cei.12267
PMID:24401077
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3992037/
Abstract

Obesity has been associated with accelerated biological ageing and immunosenescence. As the prevalence of childhood obesity is increasing, we wanted to determine if associations between obesity and immunosenescence would manifest in children. We studied 123 Mexican American adolescents aged 10-14 (mean 12·3 ± 0·7) years, with body weights ranging from 30·1 to 115·2 kg (mean 52·5 ± 14·5 kg). Blood samples were obtained to determine proportions of naive, central memory (CM), effector memory (EM), senescent and early, intermediate and highly differentiated subsets of CD4(+) and CD8(+) T cells. Overweight and obese children had significantly lowered proportions of early CD8(+) T cells (B = -11·55 and -5·51%, respectively) compared to healthy weight. Overweight children also had more EM (B = +7·53%), late (B = +8·90%) and senescent (B = +4·86%) CD8(+) T cells than healthy weight children, while obese children had more intermediate CD8(+) (B = +4·59%), EM CD8(+) (B = +5·49%), late CD4(+) (B = +2·01%) and senescent CD4(+) (B = +0·98%) T cells compared to healthy weight children. These findings withstood adjustment for potentially confounding variables, including age, gender and latent cytomegalovirus and Epstein-Barr virus infections. We conclude that excess body mass, even in adolescence, may accelerate immunosenescence and predispose children to increased risks of incurring immune-related health problems in adulthood.

摘要

肥胖与加速的生物衰老和免疫衰老有关。随着儿童肥胖症的患病率不断上升,我们想确定肥胖与免疫衰老之间的关联是否会在儿童中表现出来。我们研究了 123 名 10-14 岁的墨西哥裔美国青少年(平均 12.3 ± 0.7 岁),体重范围为 30.1 至 115.2 公斤(平均 52.5 ± 14.5 公斤)。采集血样以确定 CD4(+)和 CD8(+) T 细胞的幼稚、中央记忆(CM)、效应记忆(EM)、衰老和早期、中期和高度分化亚群的比例。与健康体重的儿童相比,超重和肥胖儿童的早期 CD8(+) T 细胞比例明显降低(分别为-11.55%和-5.51%)。超重儿童的 EM(B = +7.53%)、晚期(B = +8.90%)和衰老(B = +4.86%)CD8(+) T 细胞也比健康体重的儿童多,而肥胖儿童的中期 CD8(+)(B = +4.59%)、EM CD8(+)(B = +5.49%)、晚期 CD4(+)(B = +2.01%)和衰老 CD4(+)(B = +0.98%)T 细胞比健康体重的儿童多。这些发现经受了包括年龄、性别和潜伏的巨细胞病毒和 EBV 感染等潜在混杂变量的调整。我们的结论是,即使在青春期,过多的体重也可能加速免疫衰老,并使儿童更容易在成年后出现与免疫相关的健康问题。