Seipelt G, Ganser A, Duranceyk H, Maurer A, Ottmann O G, Hoelzer D
Department of Haematology, Johann Wolfgang Goethe University, Frankfurt am Main, Germany.
Br J Haematol. 1993 Aug;84(4):749-51. doi: 10.1111/j.1365-2141.1993.tb03157.x.
The study was undertaken to analyse whether the presence or the induction of TNF-alpha, a potent inhibitor of haemopoiesis, might affect the clinical response to treatment with interleukin-3 in patients with myelodysplastic syndromes. A total of 15 patients were treated with IL-3. Baseline serum TNF-alpha levels were elevated in MDS patients (14.2 +/- 2.4 pg/ml) compared to healthy controls (9.1 +/- 1.1 pg/ml). During IL-3 therapy TNF-alpha levels remained unchanged in 3/14 patients in whom platelet counts increased, while in non-responders TNF-alpha levels increased 1.9-fold (P < 0.025). These findings indicate that TNF-alpha not only is induced during IL-3 therapy in MDS patients but that this elevation might be associated with a poor platelet response to therapy.
开展该研究是为了分析造血功能的强效抑制剂肿瘤坏死因子-α(TNF-α)的存在或诱导是否会影响骨髓增生异常综合征患者对白细胞介素-3治疗的临床反应。共有15例患者接受了IL-3治疗。与健康对照者(9.1±1.1 pg/ml)相比,MDS患者的基线血清TNF-α水平升高(14.2±2.4 pg/ml)。在IL-3治疗期间,14例血小板计数增加的患者中有3例的TNF-α水平保持不变,而无反应者的TNF-α水平增加了1.9倍(P<0.025)。这些发现表明,TNF-α不仅在MDS患者的IL-3治疗期间被诱导,而且这种升高可能与治疗后血小板反应不佳有关。