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α干扰素在结节性非霍奇金淋巴瘤中对2'-5'寡腺苷酸合成酶的体内外诱导作用及其与临床反应的相关性

In vivo and in vitro induction of 2'-5' oligoadenylate synthetase by interferon-alpha in nodular non-Hodgkin's lymphoma and correlations with the clinical response.

作者信息

Ferbus D, Khosravi S, Dumont J, Billard C

机构信息

INSERM U. 245, Centre INSERM St-Antoine, Paris, France.

出版信息

J Biol Regul Homeost Agents. 1990 Oct-Dec;4(4):127-34.

PMID:2096597
Abstract

We investigated the correlations between the in vivo-in vitro induction of 2'-5' oligoadenylate synthetase (2-5A synthetase) by IFN-alpha in cells isolated from patients with low-grade nodular non-Hodgkin's lymphoma (NHL) and subsequent clinical responses of these patients to IFN-alpha therapy. Eleven patients were treated daily with 9 x 10(6) U of IFN-alpha 2a in a phase II trial. After an eight week treatment, four patients achieved complete remission, one a partial response, one a minor response, and five failed to respond. Basal levels of 2-5A synthetase in lymph node tumor B cells and peripheral blood mononuclear cells (PBMC) isolated before therapy differed from patient to patient and were significantly lower than in PBMC from healthy donors (P less than 0.03). In vivo single injections of 9 x 10(6) U IFN-alpha 2a induced the 2-5A synthetase in PBMC from all patients to various degrees without quantitative relation to the clinical responses. Injection of a tenfold lower dose resulted in effects of similar extent in most cases. In vitro, IFN-alpha 2a induced the 2-5A synthetase in lymph node tumor B cells isolated before therapy, and the degree of induction was significantly higher in patients who proved to respond to therapy than in patients who displayed no or minor responses (P less than 0.013). This indicates that, in nodular NHL, the 2-5A synthetase assay may have some predictive value for responsiveness to IFN-alpha therapy.

摘要

我们研究了α干扰素在低度结节性非霍奇金淋巴瘤(NHL)患者分离出的细胞中体内-体外诱导2'-5'寡腺苷酸合成酶(2-5A合成酶)与这些患者随后对α干扰素治疗的临床反应之间的相关性。在一项II期试验中,11名患者每天接受9×10⁶U的α干扰素2a治疗。经过8周治疗后,4名患者达到完全缓解,1名部分缓解,1名轻度缓解,5名无反应。治疗前分离出的淋巴结肿瘤B细胞和外周血单个核细胞(PBMC)中2-5A合成酶的基础水平因患者而异,且显著低于健康供体的PBMC(P<0.03)。体内单次注射9×10⁶Uα干扰素2a可使所有患者的PBMC中2-5A合成酶不同程度地诱导,与临床反应无定量关系。注射剂量降低10倍在大多数情况下产生相似程度的效果。在体外,α干扰素2a可诱导治疗前分离出的淋巴结肿瘤B细胞中的2-5A合成酶,治疗有反应的患者的诱导程度显著高于无反应或轻度反应的患者(P<0.013)。这表明,在结节性NHL中,2-5A合成酶检测可能对α干扰素治疗的反应性有一定的预测价值。

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