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CD4+CD28+ T细胞水平低下是1型人类免疫缺陷病毒感染患者高死亡率的独立预测指标。

A low level of CD4+CD28+ T cells is an independent predictor of high mortality in human immunodeficiency virus type 1-infected patients.

作者信息

Ostrowski Sisse R, Gerstoft Jan, Pedersen Bente K, Ullum Henrik

机构信息

Department of Infectious Diseases, Rigshospitalet, Copenhagen, Denmark.

出版信息

J Infect Dis. 2003 Jun 1;187(11):1726-34. doi: 10.1086/375239. Epub 2003 May 15.

Abstract

This study investigated coexpression of CD28, CD45RA, and CD45RO on CD4(+) and CD8(+) cells in 107 human immunodeficiency virus (HIV) type 1-infected patients, who were followed-up prospectively and were not treated with highly active antiretroviral therapy, and 65 control subjects. The most important novel finding was that a 50% reduction in CD4(+)CD28(+) cells predicted increased mortality (relative hazards [HR], 1.6; 95% confidence interval [CI], 1.0-2.6; P=.04), even after adjusting for the CD4(+) cell counts, virus load, beta(2)-microglobulin and hemoglobin levels, and HIV disease stage. Patients with progressed HIV infection had decreased concentrations of all studied cell subsets. Concerning the proportions of cells, only CD4(+)CD28(+), CD4(+)CD45RA(+), and CD8(+)CD45RO(+) cells decreased with HIV progression. Low proportions of CD4(+)CD45RA(+), CD8(+)CD45RA(+), and CD8(+)CD45RO(+) cells predicted mortality only in univariate but not in multivariate Cox analyses. If our results are confirmed in other studies, coexpression of CD28 on CD4(+) cells may be a useful marker to evaluate HIV progression.

摘要

本研究调查了107例未接受高效抗逆转录病毒治疗且接受前瞻性随访的1型人类免疫缺陷病毒(HIV)感染患者以及65名对照者CD4(+)和CD8(+)细胞上CD28、CD45RA和CD45RO的共表达情况。最重要的新发现是,即使在对CD4(+)细胞计数、病毒载量、β2-微球蛋白和血红蛋白水平以及HIV疾病分期进行校正后,CD4(+)CD28(+)细胞减少50%仍预示着死亡率增加(相对危险度[HR],1.6;95%置信区间[CI],1.0 - 2.6;P = 0.04)。HIV感染进展的患者所有研究的细胞亚群浓度均降低。关于细胞比例,只有CD4(+)CD28(+)、CD4(+)CD45RA(+)和CD8(+)CD45RO(+)细胞比例随HIV进展而降低。低比例的CD4(+)CD45RA(+)、CD8(+)CD45RA(+)和CD8(+)CD45RO(+)细胞仅在单变量Cox分析中预示死亡率,而在多变量Cox分析中则不然。如果我们的结果在其他研究中得到证实,CD4(+)细胞上CD28的共表达可能是评估HIV进展的一个有用标志物。

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