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B淋巴细胞慢性淋巴细胞白血病(B-CLL)细胞对氟达拉滨和干扰素的体外敏感性

In vitro sensitivity of B-CLL cells to fludarabine and interferons.

作者信息

Di Raimondo F, Palumbo G A, Romeo M A, Cacciola E, Milone G, Impera S, Giustolisi R, Cacciola E

机构信息

Institute of Hematology, Ospedale Ferrarotto, University of Catania, Italy.

出版信息

Leuk Lymphoma. 1995 May;17(5-6):449-53. doi: 10.3109/10428199509056856.

Abstract

In this study we evaluated the cytotoxicity of Fludarabine (FAMP) both alone and in combination with alpha and beta interferon (IFN) against B-cells from patients affected by chronic lymphocytic leukemia (CLL). We used an in vitro colorimetric assay based on the bioreduction of the tetrazolium salt XTT by viable cells. Fludarabine concentrations ranging from 0.03 to 30 microM were tested on cells collected from 22 B-CLL patients. For each fludarabine concentration, 800 I.U. of either alpha or beta IFN were added. Interferon alone did not exert any cytotoxic effect, while Fludarabine showed a strong cytotoxicity against B-CLL cells. The concentration of Fludarabine required to induce a 50% cytotoxicity (IC50) was below 3 microM (the achievable serum level after standard dose in vivo administration) for 19 out of 22 patients. After IFNs supplementation to Fludarabine, it was possible to identify three groups of samples. The first in which IFNs addition did not produce almost any significant change in Fludarabine cytotoxicity (13/22), the second in which there was an improvement in FAMP IC50 (6/22), and finally the third group in which IFNs worsened it (3/22). Stage of disease was the only identified factor accounting for these different results. The second group included samples from 5 patients at stage A and one at stage B, while in the third group all three samples were from patients at stage C. Interferon-alpha and -beta induced the same degree of FAMP IC50 variation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在本研究中,我们评估了氟达拉滨(FAMP)单独及与α和β干扰素(IFN)联合使用时对慢性淋巴细胞白血病(CLL)患者B细胞的细胞毒性。我们采用了一种基于活细胞对四唑盐XTT进行生物还原的体外比色测定法。对从22例B-CLL患者采集的细胞测试了浓度范围为0.03至30微摩尔的氟达拉滨。对于每个氟达拉滨浓度,添加800国际单位的α或β干扰素。单独的干扰素未产生任何细胞毒性作用,而氟达拉滨对B-CLL细胞显示出强烈的细胞毒性。22例患者中有19例诱导50%细胞毒性(IC50)所需的氟达拉滨浓度低于3微摩尔(体内标准剂量给药后可达到的血清水平)。在氟达拉滨中添加干扰素后,可识别出三组样本。第一组中添加干扰素几乎未使氟达拉滨细胞毒性产生任何显著变化(13/22),第二组中FAMP的IC50有所改善(6/22),最后第三组中干扰素使其恶化(3/22)。疾病分期是唯一确定的导致这些不同结果的因素。第二组包括来自5例A期患者和1例B期患者的样本,而第三组的所有三个样本均来自C期患者。α干扰素和β干扰素诱导的FAMP IC50变化程度相同。(摘要截断于250字)

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