首页> 外文期刊>Nuclearmedicine >Myeloablative radioimmunotherapy with 188Re-CD66mAb before stem cell transplantation. No increase of proinflammatory cytokine levels of TNF-alpha
【24h】

Myeloablative radioimmunotherapy with 188Re-CD66mAb before stem cell transplantation. No increase of proinflammatory cytokine levels of TNF-alpha

机译:干细胞移植前用188Re-CD66mAb进行清髓放疗。 TNF-α的促炎细胞因子水平没有增加

获取原文
获取原文并翻译 | 示例
       

摘要

AIM: Tumour necrosis factor-alpha (TNF-alpha) serum levels may increase due to intensive conditioning regimes with high-dose-chemotherapy and total body irradiation (TBI) before stem cell transplantation. This increases the risk for developing acute graft versus host disease (aGvHD) after stem cell transplantation. In this prospective study we investigated the influence of radioimmunotherapy with 188Re-CD-66-mAb on changes on TNF-alpha serum levels. PATIENTS, METHODS: In 18 patients we measured TNF-alpha before and up to 96 hours after radioimmunotherapy, in 2 patients in addition following TBI, in 9 patients also following chemotherapy. For measuring TNF-alpha we used an automated immunochemiluminescence assay (Immulite 1000 DPC Biermann, Bad Nauheim). The mean follow up period to record incidence of aGVHD was 100 days after stem cell transplantation. RESULTS: Compared to the basal levels before, the levels of TNF-alpha after conditioning with 188Re-CD-66-mAb did not increase significantly and remained in the physiological range. In contrast, these initial physiological cytokine levels increased and became pathological following 48 h after total body irradiation (13.2+/-6.6 pg/ml) and chemotherapy (10.8+/-15.7 pg/ml). In our study we found a low incidence of aGvHD (22.2%, n=4/18). CONCLUSION: These results demonstrate that additional conditioning therapy with 188Re-CD-66-mAb does not increase proinflammatory cytokine levels of TNF-alpha. This finding may indicate that additive radioimmunotherapy may not be a significant factor for increasing the rate of conditioning-associated aGvHD.
机译:目的:肿瘤坏死因子-α(TNF-alpha)血清水平可能由于干细胞移植前采用大剂量化学疗法和全身照射(TBI)的强化调理方案而增加。这增加了干细胞移植后发生急性移植物抗宿主病(aGvHD)的风险。在这项前瞻性研究中,我们调查了188Re-CD-66-mAb放射免疫疗法对TNF-α血清水平变化的影响。患者,方法:在18例患者中,我们在放射免疫治疗之前和之后96小时测量了TNF-α,在TBI之后另外2例患者中,也在化疗之后的9例患者中,测量了TNF-α。为了测量TNF-α,我们使用了自动免疫化学发光测定法(Immulite 1000 DPC Biermann,Bad Nauheim)。记录aGVHD发生率的平均随访期是干细胞移植后100天。结果:与之前的基础水平相比,用188Re-CD-66-mAb调节后的TNF-α水平没有明显增加,仍处于生理范围内。相反,这些初始生理细胞因子水平升高,并在全身照射(13.2 +/- 6.6 pg / ml)和化学疗法(10.8 +/- 15.7 pg / ml)48小时后变为病理性。在我们的研究中,我们发现aGvHD的发生率较低(22.2%,n = 4/18)。结论:这些结果表明,用188Re-CD-66-mAb进行额外的调理治疗不会增加TNF-α的促炎细胞因子水平。这一发现可能表明加成放射免疫疗法可能不是增加与条件相关的aGvHD发生率的重要因素。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号