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铁负荷对接受促红细胞生成素治疗的缺铁性血液透析患者外周血淋巴细胞亚群及循环细胞因子水平的影响。

Effect of iron loading on peripheral blood lymphocyte subsets and on circulating cytokine levels in iron-depleted hemodialysis patients receiving erythropoietin.

作者信息

Tsouchnikas Ioannis, Tsilipakou Maria, Daniilidis Michalis, Kyriazis Georgios, Pasadakis Ploumis, Parapanissiou Efthymia, Vargemezis Vasilios, Tsakiris Dimitrios

机构信息

Department of Nephrology, General Hospital of Veria, Veria, Greece.

出版信息

Nephron Clin Pract. 2007;107(3):c97-102. doi: 10.1159/000108650. Epub 2007 Sep 21.

Abstract

BACKGROUND/AIMS: High doses of iron are recommended intravenously in iron-depleted hemodialysis (HD) patients receiving recombinant erythropoietin (EPO). Iron deficiency and mainly iron overload impair cellular and humoral immune response mechanisms. Imbalances in T cell subsets are common findings in disorders of iron metabolism. The aim of this study was to evaluate the effect of iron load on peripheral blood lymphocytes subsets and on circulating cytokine levels in HD iron depleted patients, treated with EPO.

METHODS

We studied 19 stable adult HD patients, 12 males, with a mean age 59 +/- 11 years and mean HD duration 24 +/- 14 months. All patients were iron deficient and were treated with unchanged EPO dose for the last 4 months before entering the study. The administered dose of iron was infused intravenously (1,000 mg iron sucrose) in 10 doses, during 10 consecutive HD sessions. Patients were screened before the commencement of the HD session on two occasions, once prior to the first dose of iron and 2 days after the 10th dose. Hematocrit (Ht), hemoglobin (Hb), iron, serum ferritin, transferrin saturation, interleukin (IL)-2, IL-4, IL-10, interferon-gamma and tumor necrosis factor-alpha were measured. Major lymphocyte subsets (CD3+, CD19+, CD4+, CD8+, CD16+/56+, CD3+CD16+CD56+) and the ratio CD4+/CD8+ were also determined by two-color immunofluorescent analysis using flow cytometry.

RESULTS

Hb, transferrin saturation and ferritin increased significantly at the end of the study 11.2 +/- 0.9 to 11.6 +/- 0.8 g/dl, p < 0.005, 17.5 +/- 6.9 to 23.0 +/- 10.8 %, p < 0.05, and 70 +/- 43 to 349 +/- 194 microg/l, p < 0.005, respectively. IL-2 also increased significantly 27.8 +/- 15.2 to 38.9 +/- 12.8 pg/ml, p < 0.05. After iron load there was no significant change to the major lymphocyte subsets examined but a significant increase of the percentage and number of T lymphocytes with positive natural killer receptors (NKR+ T) cells was observed, 5.1 +/- 3.7% to 6.3 +/- 3.46%, p < 0.05, and 76.4 +/- 40 to 101.5 +/- 48 cells/microl, p < 0.005, respectively.

CONCLUSION

Iron load in iron-deficient EPO-treated HD patients did not produce any changes in major lymphocyte subsets in peripheral blood, but it resulted in a significant increase of NKR+ T cells, a subpopulation important for local immune responses. Iron load for a relatively short period improved anemia of HD patients and influenced the levels of the circulating IL-2, which may regulate factors affecting the survival of patients.

摘要

背景/目的:对于接受重组促红细胞生成素(EPO)治疗的缺铁性血液透析(HD)患者,建议静脉给予高剂量铁剂。缺铁,主要是铁过载会损害细胞和体液免疫反应机制。T细胞亚群失衡是铁代谢紊乱的常见表现。本研究的目的是评估铁负荷对接受EPO治疗的缺铁性HD患者外周血淋巴细胞亚群和循环细胞因子水平的影响。

方法

我们研究了19例稳定的成年HD患者,其中12例男性,平均年龄59±11岁,平均HD病程24±14个月。所有患者均缺铁,在进入研究前的最后4个月内接受不变剂量的EPO治疗。在连续10次HD治疗期间,分10次静脉输注铁剂(1000mg蔗糖铁)。在HD治疗开始前对患者进行两次筛查,一次在首次给予铁剂之前,另一次在第10剂之后2天。测量血细胞比容(Ht)、血红蛋白(Hb)、铁、血清铁蛋白、转铁蛋白饱和度、白细胞介素(IL)-2、IL-4、IL-10、干扰素-γ和肿瘤坏死因子-α。主要淋巴细胞亚群(CD3 +、CD19 +、CD4 + CD8 +、CD16 + / 56 +、CD3 + CD16 + CD56 +)以及CD4 + / CD8 +比值也通过流式细胞术的双色免疫荧光分析来确定。

结果

研究结束时,Hb、转铁蛋白饱和度和铁蛋白显著升高,分别从11.2±0.9升至11.6±0.8g/dl,p < 0.005;从17.5±6.9升至23.0±10.8%,p < 0.05;从70±43升至349±194μg/l,p < 0.005。IL-2也显著升高,从27.8±15.2升至38.9±12.8pg/ml,p < 0.05。铁负荷后,所检测的主要淋巴细胞亚群无显著变化,但观察到具有自然杀伤受体阳性(NKR + T)细胞的T淋巴细胞百分比和数量显著增加,分别从5.1±3.7%升至6.3±3.46%,p < 0.05;从76.4±40升至101.5±48细胞/μl,p < 0.005。

结论

缺铁性EPO治疗的HD患者的铁负荷在外周血主要淋巴细胞亚群中未产生任何变化,但导致NKR + T细胞显著增加,NKR + T细胞是对局部免疫反应重要的亚群。相对短时间的铁负荷改善了HD患者的贫血,并影响了循环IL-2的水平,IL-2可能调节影响患者生存的因素。

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