Shifts in Intestinal Metabolic Profile Among Kidney Transplantation Recipients with Antibody-Mediated Rejection.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Junpeng Wang, Xiaofan Zhang, Mengjun Li, Ruoying Li, Ming Zhao
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引用次数: 1

Abstract

Background: Antibody-mediated rejection (AMR) is emerging as the main cause of graft loss after kidney transplantation. Our previous study revealed the gut microbiota alternation associated with AMR in kidney transplant recipients, which was predicted to affect the metabolism-related pathways.

Methods: To further investigate the shifts in intestinal metabolic profile among kidney transplantation recipients with AMR, fecal samples from kidney transplant recipients and patients with end-stage renal disease (ESRD) were subjected to untargeted LC-MS-based metabolomics.

Results: A total of 86 individuals were enrolled in this study, including 30 kidney transplantation recipients with AMR, 35 kidney transplant recipients with stable renal function (KT-SRF), and 21 participants with ESRD. Fecal metabolome in patients with ESRD and kidney transplantation recipients with KT-SRF were parallelly detected as controls. Our results demonstrated that intestinal metabolic profile of patients with AMR differed significantly from those with ESRD. A total of 172 and 25 differential metabolites were identified in the KT-AMR group, when compared with the ESRD group and the KT-SRF group, respectively, and 14 were common to the pairwise comparisons, some of which had good discriminative ability for AMR. KEGG pathway enrichment analysis demonstrated that the different metabolites between the KT-AMR and ESRD groups or between KT-AMR and KT-SRF groups were significantly enriched in 33 or 36 signaling pathways, respectively.

Conclusion: From the metabolic point of view, our findings may provide key clues for developing effective diagnostic biomarkers and therapeutic targets for AMR after kidney transplantation.

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抗体介导的排斥反应在肾移植受者肠道代谢谱中的变化
背景:抗体介导的排斥反应(AMR)正在成为肾移植后移植物损失的主要原因。我们之前的研究揭示了与肾移植受者AMR相关的肠道微生物群变化,预计会影响代谢相关途径。方法:为了进一步研究AMR肾移植受者肠道代谢谱的变化,对肾移植受者和终末期肾病(ESRD)患者的粪便样本进行了非靶向lc - ms代谢组学分析。结果:本研究共纳入86例患者,包括30例AMR肾移植受者、35例稳定肾功能(KT-SRF)肾移植受者和21例ESRD患者。ESRD患者和KT-SRF肾移植受者的粪便代谢组被平行检测作为对照。我们的研究结果表明,AMR患者的肠道代谢谱与ESRD患者有显著差异。与ESRD组和KT-SRF组相比,KT-AMR组分别鉴定出172种和25种差异代谢物,两两比较共有14种差异代谢物,其中部分差异代谢物对AMR具有较好的鉴别能力。KEGG通路富集分析表明,KT-AMR和ESRD组、KT-AMR和KT-SRF组之间的不同代谢物分别在33条和36条信号通路中显著富集。结论:从代谢的角度来看,我们的研究结果可能为开发肾移植后AMR的有效诊断生物标志物和治疗靶点提供关键线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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