化疗诱导的骨髓抑制患者血清粒细胞集落刺激因子峰值前血清白细胞介素-6水平升高。

Y M Chen, J Whang-Peng, J M Liu, S Y Wang, C M Tsai, R P Perng
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引用次数: 5

摘要

本研究的目的是确定在化疗诱导的骨髓抑制中,是否有在造血早期发挥作用的细胞因子也与粒细胞集落刺激因子(G-CSF)一起波动。共对7例患者进行了研究。所有患者均接受3 d静脉注射联合化疗。化疗前监测患者的绝对中性粒细胞计数(ANC)、血小板计数、血清G-CSF、白细胞介素-6 (IL-6)、IL-3和IL-1 α,此后整个治疗过程中每天或每隔一天监测一次,直至ANC恢复正常。结果显示,7例患者血清IL-6水平均在中性粒细胞最低点升高之前或同时升高。在7名患者中,有6名患者IL-6的升高也与血小板水平的最低点相关。血清IL-6升高在中性粒细胞减少期和血小板减少期均有统计学意义。7例患者血清IL-3水平均低于最低可检测浓度。6例患者血清IL-1 α低于最低可检测浓度,其余患者无明显波动。因此,本研究证明了在化疗诱导的骨髓抑制中,细胞因子波动的时间顺序,IL-6在G-CSF之前达到峰值。根据这一发现,当细胞因子用于预防骨髓抑制或加速其恢复时,按顺序使用细胞因子的组合可能是合乎逻辑的,例如最初使用IL-6然后使用G-CSF。
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Elevation of serum interleukin-6 levels before peak of serum granulocyte colony-stimulating factor level in chemotherapy-induced myelosuppressive patients.

The aim of this study was to ascertain whether any cytokines that function in earlier stages of hematopoiesis also fluctuate in conjunction with granulocyte colony-stimulating factor (G-CSF) in chemotherapy-induced myelosuppression. A total of seven patients were studied. All patients received 3 days of intravenous injection of combination chemotherapy. Patients' absolute neutrophil count (ANC), platelet count, serum G-CSF, interleukin-6 (IL-6), IL-3, and IL-1 alpha were monitored before chemotherapy, and then daily or every other day thereafter during the entire treatment course until the ANC returned to normal. The results showed very obvious elevation of serum IL-6 level before or concurrent with the elevation of serum G-CSF levels at the neutrophil nadir in all seven patients. The rise of IL-6 also correlated with nadir platelet levels in six of seven patients. The finding of serum IL-6 elevation was statistically significant both in neutropenic and thrombocytopenic stages. Serum IL-3 level was below minimum detectable concentrations in all seven patients. Serum IL-1 alpha was below minimum detectable concentration in six patients and demonstrated no obvious fluctuation in the remaining patient. Therefore, the present study demonstrated the chronological time sequence of cytokine fluctuation, IL-6 peak before G-CSF, in chemotherapy-induced myelosuppression. According to this finding, when cytokines are used for prevention of myelosuppression or for acceleration of its recovery, it may be logical to use a combination of cytokines in sequence, such as IL-6 initially followed by G-CSF.

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