Ganeshaguru K, de Mel W C, Sissolak G, Catovsky D, Dearden C E, Mehta A B, Hoffbrand A V
Department of Haematology, Royal Free Hospital School of Medicine, London.
Br J Haematol. 1992 Feb;80(2):194-8. doi: 10.1111/j.1365-2141.1992.tb08900.x.
2',5'-oligoadenylate synthetase (2-5OAS) has been studied in peripheral blood mononuclear cells from nine patients with hairy cell leukaemia (HCL) receiving therapy with the adenosine deaminase inhibitor deoxycoformycin (dCF) or alpha interferon (alpha-IFN). 2-5OAS mRNA was assayed by dot-blot hybridization. Increase of 2-5OAS mRNA level was seen in six patients with HCL treated with dCF and in one patient treated with alpha-IFN who responded to therapy. A patient with a variant form of HCL treated with dCF and the second patient treated with alpha-IFN did not show an increase of 2-5OAS mRNA and neither responded to therapy. The 15 other patients with T or B-chronic lymphoblastic leukaemia (CLL), T-acute lymphoblastic leukaemia (ALL), adult T-cell leukaemia lymphoma (ATLL), non-Hodgkins lymphoma (NHL), Sezary and T or B-prolymphocytic leukaemia (PLL) treated with dCF did not show an increase in 2-5OAS, though four patients, all with T-cell tumours, responded clinically. 2-5OAS activity is known to be stimulated by alpha-IFN and recent work suggests that this rise in 2-5OAS may result in increased cleavage of mRNA for tumour necrosis factor (TNF) and other cytokines on which autocrine growth and proliferation of the tumour cells are dependent. By analogy, we suggest that one mechanism of action of dCF in hairy cell leukaemia may be to break down an autocrine growth loop for TNF or other cytokines. An alternative explanation for these observations is that cytokines released from hairy cells in the bone marrow killed by dCF induce a rise in 2-5OAS in circulating leucocytes.
对9例毛细胞白血病(HCL)患者的外周血单核细胞进行了研究,这些患者正在接受腺苷脱氨酶抑制剂去氧助间型霉素(dCF)或α干扰素(α-IFN)治疗。通过斑点杂交法检测2-5寡腺苷酸合成酶(2-5OAS)mRNA。在用dCF治疗的6例HCL患者以及1例对治疗有反应的接受α-IFN治疗的患者中,观察到2-5OAS mRNA水平升高。1例接受dCF治疗的HCL变异型患者和另1例接受α-IFN治疗的患者未显示2-5OAS mRNA升高,且均对治疗无反应。其他15例患有T或B细胞慢性淋巴细胞白血病(CLL)、T细胞急性淋巴细胞白血病(ALL)、成人T细胞白血病淋巴瘤(ATLL)、非霍奇金淋巴瘤(NHL)、Sezary综合征以及T或B原淋巴细胞白血病(PLL)并接受dCF治疗的患者,尽管有4例患者(均为T细胞肿瘤)临床有反应,但未显示2-5OAS升高。已知α-IFN可刺激2-5OAS活性,最近的研究表明,2-5OAS的这种升高可能导致肿瘤坏死因子(TNF)和其他细胞因子的mRNA裂解增加,而肿瘤细胞的自分泌生长和增殖依赖于这些细胞因子。由此类推,我们认为dCF在毛细胞白血病中的一种作用机制可能是打破TNF或其他细胞因子的自分泌生长环。对这些观察结果的另一种解释是,被dCF杀死的骨髓中的毛细胞释放的细胞因子诱导循环白细胞中2-5OAS升高。