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T淋巴细胞共刺激后细胞因子mRNA表达动力学延迟:基于环孢素A的免疫抑制疗效的定量指标。

Delayed cytokine mRNA expression kinetics after T-lymphocyte costimulation: a quantitative measure of the efficacy of cyclosporin A-based immunosuppression.

作者信息

Härtel Christoph, Fricke Lutz, Schumacher Nina, Kirchner Holger, Müller-Steinhardt Michael

机构信息

Institute of Immunology and Transfusion Medicine, and Department of Transplantation Medicine, University of Lübeck Medical School, Ratzeburger Allee 160, 23538 Lübeck, Germany.

出版信息

Clin Chem. 2002 Dec;48(12):2225-31.

Abstract

BACKGROUND

Because cyclosporin A (CsA) and glucocorticoids inhibit the production of interleukin-2 (IL-2) and other cytokines, quantitative analysis of cytokine mRNA might constitute a pharmacodynamic measure for immunosuppressive drug effects. We investigated whether immunosuppressive drugs influence cytokine mRNA expression kinetics during T-cell costimulation.

METHODS

We used a human whole blood assay to determine basal (unstimulated) IL-2, IL-4, and tumor necrosis factor-alpha (TNF-alpha) mRNA concentrations and expression kinetics after anti-CD3/anti-CD28 monoclonal antibody costimulation in kidney transplant recipients undergoing CsA-based immunosuppressive triple therapy and in healthy controls (ex vivo study I). The effect of CsA on IL-2 mRNA expression kinetics was also determined ex vivo in patients undergoing CsA monotherapy (ex vivo study II) and after in vitro addition of CsA.

RESULTS

In ex vivo study I, basal TNF-alpha mRNA but not IL-2 and IL-4 mRNA was decreased in kidney transplant patients. We observed shifts in peak IL-2 and IL-4 (from 8 to 24 h) and TNF-alpha (from 4 to 8 h of costimulation) mRNA expression in kidney transplant patients after T-cell costimulation. In patients undergoing CsA monotherapy (ex vivo study II), the inhibitory effect of CsA was detectable as an individually delayed increase in IL-2 mRNA during costimulation. In vitro addition of CsA also induced a dose-independent displacement of IL-2 mRNA expression kinetics (i.e., a delay).

CONCLUSIONS

A delayed increase in cytokine mRNA expression during T-cell costimulation may represent a sensitive effect of immunosuppression. The single analysis of one absolute or peak mRNA value could be misleading. For prospective studies involving measurement of cytokine mRNA, we therefore suggest the parameter "area of cytokine mRNA expression over time", which should include absolute cytokine mRNA values at two different time points of mRNA kinetics.

摘要

背景

由于环孢素A(CsA)和糖皮质激素可抑制白细胞介素-2(IL-2)及其他细胞因子的产生,细胞因子mRNA的定量分析可能构成免疫抑制药物效应的药效学指标。我们研究了免疫抑制药物在T细胞共刺激过程中是否会影响细胞因子mRNA的表达动力学。

方法

我们采用人全血检测法,测定接受基于CsA的免疫抑制三联疗法的肾移植受者和健康对照者(体外研究I)在抗CD3/抗CD28单克隆抗体共刺激后基础(未刺激)IL-2、IL-4和肿瘤坏死因子-α(TNF-α)mRNA浓度及表达动力学。还在接受CsA单一疗法的患者中进行体外研究(体外研究II),并在体外添加CsA后,测定CsA对IL-2 mRNA表达动力学的影响。

结果

在体外研究I中,肾移植患者基础TNF-α mRNA水平降低,但IL-2和IL-4 mRNA水平未降低。我们观察到肾移植患者在T细胞共刺激后,IL-2和IL-4(从8小时至24小时)以及TNF-α(从共刺激4小时至8小时)mRNA表达峰值出现偏移。在接受CsA单一疗法的患者中(体外研究II),CsA的抑制作用表现为共刺激期间IL-2 mRNA单独延迟增加。体外添加CsA也会导致IL-2 mRNA表达动力学出现剂量依赖性偏移(即延迟)。

结论

T细胞共刺激期间细胞因子mRNA表达延迟增加可能是免疫抑制的一种敏感效应。仅分析一个绝对或峰值mRNA值可能会产生误导。因此,对于涉及细胞因子mRNA测量的前瞻性研究,我们建议采用“细胞因子mRNA随时间的表达面积”这一参数,该参数应包括mRNA动力学两个不同时间点的绝对细胞因子mRNA值。

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