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神经炎症性疾病发病机制中的微生物群-肠道-脑-免疫接口:新兴文献的叙述性综述。

The microbiota-gut-brain-immune interface in the pathogenesis of neuroinflammatory diseases: a narrative review of the emerging literature.

机构信息

The Frame-Corr Laboratory, Department of Clinical Research and Leadership, The George Washington University School of Medicine and Health Sciences, Washington, DC, United States.

Department of Biotechnology, Harrisburg University of Science and Technology, Harrisburg, PA, United States.

出版信息

Front Immunol. 2024 May 16;15:1365673. doi: 10.3389/fimmu.2024.1365673. eCollection 2024.

Abstract

IMPORTANCE

Research is beginning to elucidate the sophisticated mechanisms underlying the microbiota-gut-brain-immune interface, moving from primarily animal models to human studies. Findings support the dynamic relationships between the gut microbiota as an ecosystem (microbiome) within an ecosystem (host) and its intersection with the host immune and nervous systems. Adding this to the effects on epigenetic regulation of gene expression further complicates and strengthens the response. At the heart is inflammation, which manifests in a variety of pathologies including neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, and Multiple Sclerosis (MS).

OBSERVATIONS

Generally, the research to date is limited and has focused on bacteria, likely due to the simplicity and cost-effectiveness of 16s rRNA sequencing, despite its lower resolution and inability to determine functional ability/alterations. However, this omits all other microbiota including fungi, viruses, and phages, which are emerging as key members of the human microbiome. Much of the research has been done in pre-clinical models and/or in small human studies in more developed parts of the world. The relationships observed are promising but cannot be considered reliable or generalizable at this time. Specifically, causal relationships cannot be determined currently. More research has been done in Alzheimer's disease, followed by Parkinson's disease, and then little in MS. The data for MS is encouraging despite this.

CONCLUSIONS AND RELEVANCE

While the research is still nascent, the microbiota-gut-brain-immune interface may be a missing link, which has hampered our progress on understanding, let alone preventing, managing, or putting into remission neurodegenerative diseases. Relationships must first be established in humans, as animal models have been shown to poorly translate to complex human physiology and environments, especially when investigating the human gut microbiome and its relationships where animal models are often overly simplistic. Only then can robust research be conducted in humans and using mechanistic model systems.

摘要

重要性

研究开始阐明微生物群-肠道-大脑-免疫界面背后的复杂机制,从主要的动物模型转向人类研究。研究结果支持了肠道微生物群作为一个生态系统(微生物组)在宿主生态系统中的动态关系及其与宿主免疫系统和神经系统的交叉关系。将这一点添加到对基因表达的表观遗传调控的影响中,进一步使反应变得复杂和加强。核心是炎症,它表现在多种病理学中,包括神经退行性疾病,如阿尔茨海默病、帕金森病和多发性硬化症(MS)。

观察结果

一般来说,迄今为止的研究是有限的,并且集中在细菌上,这可能是由于 16s rRNA 测序的简单性和成本效益,尽管其分辨率较低,无法确定功能能力/改变。然而,这忽略了所有其他微生物群,包括真菌、病毒和噬菌体,它们正成为人类微生物群的关键成员。大部分研究都是在临床前模型中进行的,或者是在世界上较为发达的地区进行的小规模人类研究中进行的。观察到的关系很有前景,但目前还不能认为是可靠或可推广的。具体来说,目前还不能确定因果关系。在阿尔茨海默病之后,对帕金森病的研究较多,而对多发性硬化症的研究较少。尽管如此,多发性硬化症的数据还是令人鼓舞的。

结论和相关性

虽然研究仍处于起步阶段,但微生物群-肠道-大脑-免疫界面可能是一个缺失的环节,这阻碍了我们在理解这些疾病方面的进展,更不用说预防、管理或缓解神经退行性疾病了。首先必须在人类中建立关系,因为动物模型已被证明与复杂的人类生理学和环境相关性较差,特别是在研究动物模型通常过于简单的人类肠道微生物群及其关系时。只有这样,才能在人类中进行强有力的研究,并使用机制模型系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/11137262/72d511c8d9e9/fimmu-15-1365673-g001.jpg

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