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从传染病角度看微生物组与异基因造血干细胞移植

An infectious diseases perspective on the microbiome and allogeneic stem cell transplant.

机构信息

Department of Infectious Diseases, Austin Health.

Department of Infectious Diseases.

出版信息

Curr Opin Infect Dis. 2020 Dec;33(6):426-432. doi: 10.1097/QCO.0000000000000683.

Abstract

PURPOSE OF REVIEW

The gut microbiome presents a novel source of diagnostic and therapeutic potential to modify post allogeneic stem cell transplant complications. There is an explosion of interest in microbiome research, mostly in the form of single-centre prospective time-series cohorts utilizing a variety of sampling frequencies and metagenomic technologies to sequence the microbiome. The purpose of this review is to summarize important recent publications and contextualize them within what has already been described in this rapidly growing field.

RECENT FINDING

Results from observational human cohort and animal transplant models add to the growing body of evidence that the microbiome modulates the immunopathogenesis of posttransplant complications. This is particularly the case for recipients of grafts replete with T cells where the evidence that acute graft-versus-host disease is mediated by anaerobic commensal-associated short-chain fatty acids, which interact with mucosa-associated (CD4FOXP3) T-regulatory cells.

SUMMARY

Future human research into the role of the microbiome in allogeneic stem transplant should incorporate rigorous and considered experimental design in addition to next-generation sequencing technology to better portray microbiome functional potential and active gene expression. In combination with host immune phenotyping, which would facilitate a robust understanding of the host--microbiome interaction that is required before meaningful translation into clinical diagnostics and therapeutics can be expected.

摘要

目的综述

肠道微生物组为改变异基因干细胞移植后并发症提供了一种新的诊断和治疗潜力来源。人们对微生物组研究的兴趣呈爆炸式增长,主要形式是采用各种采样频率和宏基因组技术对微生物组进行测序的单中心前瞻性时间序列队列研究。本文旨在总结重要的最新文献,并将其置于该快速发展领域已有的描述范围内。

最近的发现

来自观察性人类队列和动物移植模型的结果增加了越来越多的证据,证明微生物组调节移植后并发症的免疫发病机制。对于充满 T 细胞的移植物受者尤其如此,有证据表明急性移植物抗宿主病是由与粘膜相关的(CD4FOXP3)T 调节细胞相互作用的厌氧共生短链脂肪酸介导的。

总结

未来对微生物组在异基因干细胞移植中的作用的人类研究应将严格和经过深思熟虑的实验设计与下一代测序技术相结合,以更好地描绘微生物组的功能潜力和活性基因表达。结合宿主免疫表型,这将有助于对宿主-微生物组相互作用有一个稳健的理解,这是在有意义地转化为临床诊断和治疗之前所必需的。

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