M Meffert, E L Hanninen, T Menzel, A Schomburg, S Duensing, I Dallmann, J Grosse, S Vocke, J Buer, M Deckert
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引用次数: 11
摘要
采用低剂量人重组白细胞介素-2 (il -2)皮下注射治疗肾癌患者,测定血清白细胞介素-6 (IL-6)浓度。在所有患者中,经酶联免疫吸附试验(ELISA)测定,给予il -2导致IL-6血清水平在4至6小时内显著升高至峰值。与首次给药相比,重复给药il -2可显著降低IL-6血清峰值。以浓度曲线下面积(AUC)表示的IL-6累积释放量与il -2剂量分布无关(1000万IU il -2/m2 vs 2000万IU il -2/m2), IL-6血清峰值与剂量无直接关系。先前的il -2免疫治疗对il -2诱导的IL-6释放没有可测量的影响,而类固醇导致继发性IL-6的显著抑制与il -2治疗的反应或il -2治疗的肾癌患者的生存无关。
In vivo time and dose dependency of interleukin-6 secretion in response to low-dose subcutaneous recombinant interleukin-2.
Serum concentrations of Interleukin-6 (IL-6) were determined in renal cell carcinoma patients treated with low-dose subcutaneous human recombinant interleukin-2 (rIL-2). In all patients, administration of rIL-2 resulted in a significant increase in IL-6 serum levels to peak values within 4 to 6 hours as measured by enzyme-linked immunosorbent assays (ELISA). Repetitive administration of rIL-2 induced significantly lower IL-6 serum peaks when compared to the initial administration of rIL-2. Cumulative IL-6 release, as expressed by the area under the concentration curve (AUC), appeared to be independent of rIL-2 dose distribution (10 million IU rIL-2/m2 versus 20 million IU rIL-2/m2), and IL-6 serum peaks showed no direct dose dependency. Prior rIL-2 immunotherapy had no measurable effect on rIL-2 induced IL-6 release, while steroids resulted in a significant suppression of secondary IL-6 did not correlate with response to rIL-2 therapy or survival of rIL-2 treated renal cell carcinoma patients.