首页> 美国卫生研究院文献>Theranostics >Novel spheroid reservoir bioartificial liver improves survival of nonhuman primates in a toxin-induced model of acute liver failure
【2h】

Novel spheroid reservoir bioartificial liver improves survival of nonhuman primates in a toxin-induced model of acute liver failure

机译:在毒素诱导的急性肝功能衰竭模型中新型球状水库生物人工肝改善了非人类灵长类动物的存活率

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。
获取外文期刊封面目录资料

摘要

This study aims to evaluate the effectiveness and safety of the spheroid reservoir bioartificial liver (SRBAL) with porcine hepatocyte organoids in a preclinical nonhuman primate model of acute liver failure (ALF).>Methods: Thirty healthy rhesus monkeys were infused with α-amanitin and lipopolysaccharide and randomized into five groups (ALF alone control group; sham no-cell SRBAL treatment group; groups A, B and C with SRBAL treatment started at 12 h, 24 h and 36 h after induction of ALF, respectively). Animals were continuously treated with the SRBAL device for 6 h and followed for up to 336 h.>Results: Survival of ALF monkeys improved with hepatocyte SRBAL treatment compared to control groups. Blood ammonia and total bilirubin were lower, and albumin levels were higher in all hepatocyte SRBAL treatment groups. No evidence of porcine endogenous retrovirus was identified in monkey liver or blood after SRBAL treatment. Titers of monkey antibody (IgG, IgM) did not rise after SRBAL treatment. In survival cases, the proportion of necrotic and apoptotic hepatocytes was lower in SRBAL-treated groups, with earlier liver regeneration leading to recovery. Cytokines TNF-α, IL-6, IL-12, IL-1β, IL-8, IFN-γ and IL-2 were ameliorated by the SRBAL treatment, while levels of M-CSF; HGF, EGF and VEGF; IL-1RA and MIF rose on priming, proliferation and the late phase of liver regeneration.>Conclusions: The benefit of SRBAL therapy included preventive effects and therapeutic effects. SRBAL improved survival rate and prolonged median survival time in a nonhuman primate model of drug-induced ALF, and these benefits declined with a delay in the initiation of therapy. Improved survival and recovery of ALF monkeys was associated with a reduction in blood ammonia levels, inhibition of the pro-inflammatory response of ALF, and provided a microenvironment more suitable for regeneration of the injured liver.
机译:本研究旨在评估在临床前非人类灵长类动物急性肝衰竭(ALF)模型中,带有猪肝细胞类器官的球状储库生物人工肝(SRBAL)的有效性和安全性。>方法:输注α-amanitin和脂多糖并随机分为五组(仅ALF对照组;假无细胞SRBAL治疗组;接受SRBAL治疗的A,B和C组在诱导ALF后12 h,24 h和36 h开始,分别)。用SRBAL装置对动物进行连续6h的治疗,随后长达336h。在所有肝细胞SRBAL治疗组中,血氨和总胆红素均较低,白蛋白水平较高。 SRBAL治疗后在猴肝或血液中未发现猪内源性逆转录病毒的证据。 SRBAL处理后,猴抗体(IgG,IgM)的滴度没有增加。在存活病例中,在SRBAL治疗组中,坏死性和凋亡性肝细胞的比例较低,肝脏再生较早导致恢复。通过SRBAL处理可改善细胞因子TNF-α,IL-6,IL-12,IL-1β,IL-8,IFN-γ和IL-2的水平,而M-CSF的水平则得到改善。 HGF,EGF和VEGF; IL-1RA和MIF在启动,增殖和肝再生的晚期阶段上升。>结论: SRBAL治疗的益处包括预防作用和治疗作用。在药物诱导的ALF的非人类灵长类动物模型中,SRBAL可提高生存率并延长中位生存时间,并且这些益处随着治疗开始的延迟而下降。 ALF猴子的存活和恢复提高与血氨水平降低,ALF促炎反应的抑制有关,并提供了更适合受伤肝脏再生的微环境。

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