首页> 外文OA文献 >Red Blood Cell Supernatant Potentiates LPS-Induced Proinflammatory Cytokine Response From Peripheral Blood Mononuclear Cells
【2h】

Red Blood Cell Supernatant Potentiates LPS-Induced Proinflammatory Cytokine Response From Peripheral Blood Mononuclear Cells

机译:红细胞上清液可增强LPS诱导的外周血单个核细胞的促炎性细胞因子反应

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

Allogeneic blood transfusion has an immunomodulatory capacity on its recipients through accumulation of immunologically active substances with blood storage, and prestorage leukoreduction reduces many of these mediators. We investigated lipopolysaccharide (LPS)-induced cytokine response of peripheral blood mononuclear cells (PBMCs) exposed to packed red blood cell (PRBC) supernatants from leukoreduced (LR) or non-leukoreduced (NLR) units with variable duration of storage. PRBC units were collected with or without leukoreduction on Day 0 before routine storage. The plasma fraction (supernatant) was isolated from LR and NLR units after 1 day (D1) or 42 days (D42) of storage and exposed to PBMCs versus control media for 24 h, then with LPS for an additional 24 h. Cell supernatants were analyzed for IL-1β, IL-6, IL-8, IL-10, and TNF-α by cytokine bead array. IL-1β, TNF-α, and IL-6 were significantly elevated in PRBC groups versus control. D42 NLR PRBC supernatant significantly increased secretion of IL-1β and IL-6 compared to D1 NLR PRBC supernatant. LR significantly attenuated the cytokine response of IL-1β. Thus, PRBC supernatant potentiates proinflammatory LPS-induced cytokine secretion from PBMCs. This response is accentuated with storage duration and partially attenuated with leukoreduction. These findings may partially explain the immune activation seen clinically after blood transfusion.
机译:同种异体输血通过在血液中积累具有免疫活性的物质而对受者具有免疫调节能力,而蓄积前的白细胞减少减少了许多这些介体。我们调查了脂多糖(LPS)诱导的外周血单核细胞(PBMC)的细胞因子反应,暴露于来自白细胞减少的(LR)或非白细胞减少的(NLR)单位的堆积红细胞(PRBC)上清液,具有可变的储存时间。在常规储存前第0天收集PRBC单位,有或无白细胞减少。储存1天(D1)或42天(D42)后,从LR和NLR单位中分离血浆级分(上清液),并与对照培养基接触PBMC 24 h,然后再与LPS接触24 h。通过细胞因子珠阵列分析细胞上清液中的IL-1β,IL-6,IL-8,IL-10和TNF-α。 PRBC组与对照组相比,IL-1β,TNF-α和IL-6明显升高。与D1 NLR PRBC上清液相比,D42 NLR PRBC上清液显着增加了IL-1β和IL-6的分泌。 LR显着减弱了IL-1β的细胞因子应答。因此,PRBC上清液可增强PBMC促炎性LPS诱导的细胞因子分泌。该反应随着贮藏时间的延长而加重,并因白细胞减少而部分减弱。这些发现可能部分解释了输血后临床上看到的免疫激活。

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