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耐受肾移植受者尿液微生物群中独特且特定的变形菌多样性。

Unique and specific Proteobacteria diversity in urinary microbiota of tolerant kidney transplanted recipients.

作者信息

Colas Luc, Mongodin Emmanuel F, Montassier Emmanuel, Chesneau Mélanie, Guerif Pierrick, Hittle Lauren, Giral Magali, Bromberg Jonathan S, Brouard Sophie

机构信息

Plateforme Transversale d'Allergologie et d'Immunologie Clinique, Institut du Thorax, CHU de Nantes, Nantes, France.

Centre de Recherche en Transplantation et Immunologie UMR1064, INSERM, Université de Nantes, Nantes, France.

出版信息

Am J Transplant. 2020 Jan;20(1):145-158. doi: 10.1111/ajt.15549. Epub 2019 Sep 9.

Abstract

Host-microbiota interactions can modulate the immune system both at local and systemic levels, with potential consequences for organ transplantation outcomes. In this study, we hypothesized that differences in the urinary microbiome following kidney transplantation would be associated with posttransplantation status: stable, minimally immunosuppressed, or tolerant. One hundred thirteen urine samples from stable (n = 51), minimally immunosuppressed (n = 19), and spontaneously tolerant (n = 16) patients, paired with age-matched controls (n = 27) were profiled and compared to each other at a taxonomic level with special interest in the immunosuppressive regimen. All comparisons and correlations were adjusted on sex and time posttransplantation. Our results highlighted a unique and specific urinary microbiota associated with spontaneous tolerance characterized by a high diversity and a clear Proteobacteria profile. Finally, we report that this profile is (1) impacted by gender, (2) inversely correlated with immunosuppressive drugs (calcineurin inhibitors and mammalian target of rapamycin inhibitors), and (3) stable in time.

摘要

宿主-微生物群相互作用可在局部和全身水平调节免疫系统,对器官移植结果产生潜在影响。在本研究中,我们假设肾移植后尿微生物群的差异与移植后状态相关:稳定、免疫抑制最小或耐受。对来自稳定状态(n = 51)、免疫抑制最小状态(n = 19)和自发耐受状态(n = 16)患者的113份尿液样本,以及年龄匹配的对照组(n = 27)进行分析,并在分类水平上相互比较,特别关注免疫抑制方案。所有比较和相关性均根据性别和移植后时间进行调整。我们的结果突出显示了一种与自发耐受相关的独特且特定的尿微生物群,其特征为高度多样性和明确的变形菌门特征。最后,我们报告该特征:(1)受性别影响,(2)与免疫抑制药物(钙调神经磷酸酶抑制剂和雷帕霉素靶蛋白抑制剂)呈负相关,(3)随时间稳定。

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