首页> 美国卫生研究院文献>Mediators of Inflammation >Induction of circulating phospholipase A2 by intravenous administration of recombinant human tumour necrosis factor
【2h】

Induction of circulating phospholipase A2 by intravenous administration of recombinant human tumour necrosis factor

机译:静脉内注射重组人肿瘤坏死因子诱导循环磷脂酶A2

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We have examined the effects of intravenous infusion of recombinant human tumour necrosis factor (rh-TNF) on serum activity of phospholipase A2 (PLA2) in patients with malignancies. Nine patients received a 24 h continuous intravenous infusion ranging from 1.0 × 105 U/m2 to 3.0 × 105 U/m2; 14 patients received a 5 day continuous intravenous infusion ranging from 0.5 × 105 U/m2/day to 3.0 105 U/m2/day. Twenty one of 23 patients responded with marked increases in serum PLA2 activity that were detectable 3 h after the beginning of the rh-TNF infusion and reached maximum levels at 18 h with a mean increase of 16.2-fold. In patients receiving a 5 day rh-TNF infusion, the highest levels of PLA2 were observed after the first day of infusion. Serum PLA2 activity declined continuously to 2.9-fold above baseline at the end of the infusion. A significant correlation was noted between the dose of infused rh-TNF and the maximum increase in PLA2 activity. To our knowledge, this is the first time that an association between intravenous TNF administration and induction of circulating PLA2 in man has been established.
机译:我们已经检查了静脉输注重组人肿瘤坏死因子(rh-TNF)对恶性肿瘤患者磷脂酶A2(PLA2)血清活性的影响。 9名患者接受了24小时连续静脉输注,范围从1.0×10 5 U / m 2 到3.0×10 5 U / m 2 ; 14例患者接受5天连续静脉输注,范围从0.5×10 5 U / m 2 /天到3.0 10 5 U / m < sup> 2 /天。 rh-TNF输注开始后3小时,有23例患者中有21例血清PLA2活性显着升高,并在18 h达到最高水平,平均升高16.2倍。在接受5天rh-TNF输注的患者中,输注第一天后观察到最高的PLA2水平。输注结束时,血清PLA2活性持续下降至基线以上2.9倍。在注入的rh-TNF剂量和PLA2活性的最大增加之间发现了显着的相关性。据我们所知,这是首次建立静脉内给予TNF与诱导人体内循环PLA2之间的联系。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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