Nachbaur D, Gratwohl A, Herold M, Tichelli A, Slanicka M, Nissen C, Niederwieser D, Speck B
University Hospital, Department of Internal Medicine, Innsbruck, Austria.
Ann Hematol. 1993 Feb;66(2):71-5. doi: 10.1007/BF01695887.
A 37-year-old woman with severe aplastic anemia (SAA), who had relapsed 6 years after antilymphocyte globulin therapy, was treated with intravenous recombinant human IL-3 (4 micrograms/kg/d) for 21 days. Subsequently, long-term therapy with subcutaneous rhIL-3 at the highest dose level tested so far (16 micrograms/kg/d) was initiated in order to maintain growth-factor response. Therapy was discontinued on day 73 due to progressive thrombocytopenia and increased petechial bleeding. Both treatment schedules resulted in a transient increase in leukocytes (twofold) due to an increase in monocytes, neutrophils, and eosinophils. RhIL-3 had no effect on hemoglobin values or platelet counts and only marginally improved colony formation of bone marrow CFU-GM in response to rhGM-CSF. Side effects of both treatment schedules were mild and did not exceed WHO grade II. Steady-state serum concentrations of IL-3, which are able to stimulate hematopoiesis in vitro (i.e. > 1 ng/ml), were achieved by both low- and high-dose treatment, although high-dose treatment resulted in markedly higher serum levels of IL-3. On measuring cytokine serum levels (neopterin, IL-1 beta, IL-6, sIL-2R, GM-CSF, TNF-alpha, IFN-gamma) we noticed a different cytokine pattern with both treatment modalities, resulting in a moderate induction of TNF-alpha and IFN-gamma during low-dose, intravenous treatment, whereas during subcutaneous, high-dose treatment a profound increase of IL-6, sIL-2R, and, to a lesser extent, neopterin was detected. These results in a single patient with SAA indicate that further studies on IL-3 serum levels and IL-3-induced secondary cytokines in a larger group of patients are needed to optimize growth-factor treatment and to better understand the in vivo biological activity of IL-3.
一名37岁的严重再生障碍性贫血(SAA)女性患者,在接受抗淋巴细胞球蛋白治疗6年后复发,接受了21天的静脉注射重组人IL-3(4微克/千克/天)治疗。随后,为维持生长因子反应,开始采用迄今为止测试的最高剂量水平(16微克/千克/天)的皮下rhIL-3进行长期治疗。由于进行性血小板减少和瘀点出血增加,治疗在第73天停止。两种治疗方案均因单核细胞、中性粒细胞和嗜酸性粒细胞增加导致白细胞短暂增加(两倍)。RhIL-3对血红蛋白值或血小板计数没有影响,仅对rhGM-CSF刺激的骨髓CFU-GM集落形成有轻微改善。两种治疗方案的副作用均较轻,未超过世界卫生组织二级。低剂量和高剂量治疗均达到了能够在体外刺激造血的IL-3稳态血清浓度(即>1纳克/毫升),尽管高剂量治疗导致IL-3血清水平明显更高。在测量细胞因子血清水平(新蝶呤、IL-1β、IL-6、sIL-2R、GM-CSF、TNF-α、IFN-γ)时,我们注意到两种治疗方式的细胞因子模式不同,低剂量静脉治疗期间TNF-α和IFN-γ有中度诱导,而在皮下高剂量治疗期间,检测到IL-6、sIL-2R以及程度较轻的新蝶呤有显著增加。该SAA单例患者的这些结果表明,需要在更大规模的患者群体中进一步研究IL-3血清水平和IL-3诱导的次级细胞因子,以优化生长因子治疗并更好地理解IL-3的体内生物学活性。