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接受重组白细胞介素-2免疫治疗患者的血清细胞因子和急性期反应物水平与体重及血清白蛋白变化的相关性

Correlation of serum cytokine and acute phase reactant levels with alterations in weight and serum albumin in patients receiving immunotherapy with recombinant IL-2.

作者信息

Deehan D J, Heys S D, Simpson W, Herriot R, Broom J, Eremin O

机构信息

Department of Surgery, University of Aberdeen, UK.

出版信息

Clin Exp Immunol. 1994 Mar;95(3):366-72. doi: 10.1111/j.1365-2249.1994.tb07005.x.

Abstract

Recombinant IL-2 (rIL-2) has been used alone or in combination with other chemotherapeutic agents to enhance host defences against cancer. Prolonged administration of high doses, required for clinical efficacy, may precipitate serious dose-limiting toxicity. rIL-2-induced 'vascular leak syndrome' leads to hypotension, renal insufficiency, respiratory disturbances and other organ dysfunctions. Serial measurements of serum cytokines and the acute phase protein C-reactive protein (CRP) were performed on nine patients who received high-dose i.v. continuous therapy with rIL-2. The influence of these immunological parameters upon alterations in patients' weight and serum albumin, as indicators of toxicity, was assessed. All patients experienced weight increases during the cycle (3-11% of total body weight). The serum levels of tumour necrosis factor (TNF-alpha) and CRP were highly predictive of alterations in patients' weight (both P < 0.001), while no correlation was found with IL-6 and weight change. Serum albumin fell linearly throughout the infusion cycle, but this showed no correlation with variations in serum levels of IL-6, TNF-alpha, or CRP. The complement components C3 and C4 were significantly reduced at the end of the infusion, suggesting a possible role for this cascade system in mediating these clinical changes. The strong association between serum TNF-alpha and weight change, not previously documented, further supports the hypothesis that TNF-alpha is a key mediator in the pathogenesis of the 'vascular leak syndrome'.

摘要

重组白细胞介素-2(rIL-2)已被单独使用或与其他化疗药物联合使用,以增强宿主对癌症的防御能力。临床疗效所需的高剂量长时间给药可能会引发严重的剂量限制性毒性。rIL-2诱导的“血管渗漏综合征”会导致低血压、肾功能不全、呼吸紊乱和其他器官功能障碍。对9名接受大剂量静脉持续rIL-2治疗的患者进行了血清细胞因子和急性期蛋白C反应蛋白(CRP)的系列测量。评估了这些免疫参数对作为毒性指标的患者体重和血清白蛋白变化的影响。所有患者在治疗周期内体重均增加(占总体重的3 - 11%)。肿瘤坏死因子(TNF-α)和CRP的血清水平对患者体重变化具有高度预测性(两者P < 0.001),而未发现与IL-6和体重变化存在相关性。在整个输注周期中血清白蛋白呈线性下降,但这与IL-6、TNF-α或CRP血清水平的变化无相关性。输注结束时补体成分C3和C4显著降低,表明该级联系统在介导这些临床变化中可能发挥作用。血清TNF-α与体重变化之间的强关联(此前未记录)进一步支持了TNF-α是“血管渗漏综合征”发病机制中的关键介质这一假说。

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