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Impact of the microbiota on solid organ transplant rejection.肠道菌群对实体器官移植排斥反应的影响。
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Gender issues in solid organ donation and transplantation.实体器官捐献与移植中的性别问题。
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本文引用的文献

1
Skin-restricted commensal colonization accelerates skin graft rejection.皮肤局限定植的共生菌会加速皮肤移植物排斥。
JCI Insight. 2019 Jul 16;5(15):127569. doi: 10.1172/jci.insight.127569.
2
Vendor-specific microbiome controls both acute and chronic murine lung allograft rejection by altering CD4 Foxp3 regulatory T cell levels.特定供体的微生物组通过改变 CD4 Foxp3 调节性 T 细胞水平来控制急性和慢性小鼠肺移植排斥反应。
Am J Transplant. 2019 Oct;19(10):2705-2718. doi: 10.1111/ajt.15523. Epub 2019 Aug 2.
3
Meta-omics analysis of elite athletes identifies a performance-enhancing microbe that functions via lactate metabolism.精英运动员的宏基因组分析确定了一种通过乳酸代谢发挥作用的、可提高运动表现的微生物。
Nat Med. 2019 Jul;25(7):1104-1109. doi: 10.1038/s41591-019-0485-4. Epub 2019 Jun 24.
4
Mapping human microbiome drug metabolism by gut bacteria and their genes.通过肠道细菌及其基因映射人类微生物组药物代谢。
Nature. 2019 Jun;570(7762):462-467. doi: 10.1038/s41586-019-1291-3. Epub 2019 Jun 3.
5
Mouse microbiomes: overlooked culprits of experimental variability.小鼠微生物组:实验变异性被忽视的罪魁祸首。
Genome Biol. 2019 May 29;20(1):108. doi: 10.1186/s13059-019-1723-2.
6
Structural shifts in the intestinal microbiota of rats treated with cyclosporine A after orthotropic liver transplantation.肝移植后环孢素 A 治疗大鼠肠道微生物群落结构的变化。
Front Med. 2019 Aug;13(4):451-460. doi: 10.1007/s11684-018-0675-3. Epub 2019 Apr 24.
7
Intestinal bacterial β-glucuronidase as a possible predictive biomarker of irinotecan-induced diarrhea severity.肠道细菌β-葡萄糖醛酸酶作为预测伊立替康所致腹泻严重程度的可能生物标志物。
Pharmacol Ther. 2019 Jul;199:1-15. doi: 10.1016/j.pharmthera.2019.03.002. Epub 2019 Mar 1.
8
Dysregulated Lung Commensal Bacteria Drive Interleukin-17B Production to Promote Pulmonary Fibrosis through Their Outer Membrane Vesicles.失调的肺部共生菌通过其外膜囊泡产生白细胞介素-17B 以促进肺纤维化。
Immunity. 2019 Mar 19;50(3):692-706.e7. doi: 10.1016/j.immuni.2019.02.001. Epub 2019 Feb 26.
9
Gut microbiota regulates lacteal integrity by inducing VEGF-C in intestinal villus macrophages.肠道微生物群通过诱导肠道绒毛巨噬细胞中的 VEGF-C 来调节乳管完整性。
EMBO Rep. 2019 Apr;20(4). doi: 10.15252/embr.201846927. Epub 2019 Feb 19.
10
Diet modulates colonic T cell responses by regulating the expression of a antigen.饮食通过调节 a 抗原的表达来调节结肠 T 细胞的反应。
Sci Immunol. 2019 Feb 8;4(32). doi: 10.1126/sciimmunol.aau9079.

肠道菌群对实体器官移植排斥反应的影响。

Impact of the microbiota on solid organ transplant rejection.

出版信息

Curr Opin Organ Transplant. 2019 Dec;24(6):679-686. doi: 10.1097/MOT.0000000000000702.

DOI:10.1097/MOT.0000000000000702
PMID:31577594
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7137354/
Abstract

PURPOSE OF REVIEW

The microbiota in mammalian hosts can affect maturation and function of the immune system and has been associated with health and disease. We will review new findings on how this dynamic environmental factor impacts alloimmunity and therapy in transplant hosts.

RECENT FINDINGS

The microbiota changes after transplantation and immunosuppressive therapy. New data indicate that different microbial community structures have distinct impact on graft outcome, from promoting, to inhibiting or being neutral to transplant survival. In addition, we will address reciprocal interactions between the microbiota and immunosuppressive drugs, as well as the suitability of the microbiota as a predictive biomarker and its utility as adjunct therapy in transplantation.

SUMMARY

Advances in microbiome sequencing and wider availability of gnotobiotic facilities are enabling mechanistic investigations into the commensal communities and pathways that modulate allograft outcome, responsiveness to immunosuppression and side effects of drugs. A better understanding of the functions of the microbiota may help mitigate drug toxicity, predict drug dosage and dampen alloimmunity in transplant patients.

摘要

目的综述

哺乳动物宿主中的微生物群会影响免疫系统的成熟和功能,并与健康和疾病有关。我们将回顾有关这种动态环境因素如何影响移植宿主中的同种异体免疫和治疗的新发现。

最近的发现

移植和免疫抑制治疗后,微生物群会发生变化。新数据表明,不同的微生物群落结构对移植物的结果具有不同的影响,从促进、抑制或对移植存活无影响。此外,我们将讨论微生物群与免疫抑制药物之间的相互作用,以及微生物群作为预测生物标志物的适宜性及其在移植中的辅助治疗作用。

总结

宏基因组测序技术的进步和无菌设施的广泛应用,使我们能够对调节移植物结果、对免疫抑制药物的反应性以及药物副作用的共生群落和途径进行机制研究。更好地了解微生物群的功能可以帮助减轻药物毒性、预测药物剂量并抑制移植患者的同种异体免疫。