Verhoef G, Boogaerts M
Department of Haematology, University Hospital Gasthuisberg, Leuven, Belgium.
Br J Haematol. 1991 Oct;79(2):177-84. doi: 10.1111/j.1365-2141.1991.tb04519.x.
We studied the long-term in vivo effects of recombinant granulocyte-macrophage colony stimulating factor (rhGM-CSF) on granulocyte functions in nine patients with myelodysplastic syndrome (MDS). The treatment schedule consisted of a 14 d course of rhGM-CSF (250 micrograms/m2/d s.c.) for patients with refractory anaemia (RA) and refractory anaemia with ringed sideroblasts (RARS), while patients with refractory anaemia with excess of blasts (RAEB) and refractory anaemia with excess blasts in transformation (RAEBt) received a 14 d combination course of rhGM-CSF (250 micrograms/m2 s.c.) and low dose cytosine arabinoside (20 mg/m2 s.c.). rhGM-CSF increased the mean neutrophil count from 3.9 x 10(9)/l to 44 x 10(9)/l. Significant increases of myeloperoxidase content in granulocytes occurred during treatment (P = 0.003). Phagocytosis and killing of Staph. aureus by granulocytes was markedly enhanced during treatment. Microbicidal capacity normalized in four out of six patients during GM-CSF therapy. However, chemotaxis in response to zymosan-activated serum (ZAS) and f-Met-Leu-Phe (f-MLP), was further impaired on the last day of treatment, which was associated with a marked increase in the expression of the granulocyte adhesion receptors CD11a (P = 0.01), CD11b (P = 0.002), CD11c (P = 0.00015) and CD18 (P = 0.0014). GM-CSF therapy did not cause significant changes in hexose monophosphate (HMP)-shunt activity, chemiluminescence, nor superoxide production. The present results show that in vivo administration of GM-CSF is able to repair at least in part the neutrophil anomalies in patients with myelodysplastic syndrome (MDS), which might be useful in modulating host response to infections. However, increased adherence and impaired chemotaxis may explain some toxicities observed during treatment with GM-CSF.
我们研究了重组粒细胞-巨噬细胞集落刺激因子(rhGM-CSF)对9例骨髓增生异常综合征(MDS)患者粒细胞功能的长期体内效应。治疗方案为:难治性贫血(RA)和环形铁粒幼细胞难治性贫血(RARS)患者接受为期14天的rhGM-CSF治疗(250微克/平方米/天,皮下注射),而难治性贫血伴原始细胞增多(RAEB)和转变中的难治性贫血伴原始细胞增多(RAEBt)患者接受为期14天的rhGM-CSF(250微克/平方米,皮下注射)与小剂量阿糖胞苷(20毫克/平方米,皮下注射)的联合治疗。rhGM-CSF使中性粒细胞平均计数从3.9×10⁹/升增至44×10⁹/升。治疗期间粒细胞髓过氧化物酶含量显著增加(P = 0.003)。治疗期间粒细胞对金黄色葡萄球菌的吞噬和杀伤作用明显增强。在GM-CSF治疗期间,6例患者中有4例的杀菌能力恢复正常。然而,在治疗的最后一天,对酵母聚糖激活血清(ZAS)和f-甲硫氨酰-亮氨酰-苯丙氨酸(f-MLP)的趋化性进一步受损,这与粒细胞黏附受体CD11a(P = 0.01)、CD11b(P = 0.002)、CD11c(P = 0.00015)和CD18(P = 0.0014)表达的显著增加有关。GM-CSF治疗未引起己糖磷酸(HMP)-旁路活性、化学发光或超氧化物产生的显著变化。目前的结果表明,体内给予GM-CSF能够至少部分修复骨髓增生异常综合征(MDS)患者的中性粒细胞异常,这可能有助于调节宿主对感染的反应。然而,黏附增加和趋化性受损可能解释了GM-CSF治疗期间观察到的一些毒性反应。