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微生物群与疾病:审视口腔微生物群、衰老与阿尔茨海默病之间的联系。

The microbiome and disease: reviewing the links between the oral microbiome, aging, and Alzheimer's disease.

作者信息

Shoemark Deborah K, Allen Shelley J

机构信息

School of Clinical Sciences, University of Bristol, Southmead Hospital, Bristol, UK.

出版信息

J Alzheimers Dis. 2015;43(3):725-38. doi: 10.3233/JAD-141170.

Abstract

This review, gathered from diverse sources, shows how our microbiome influences health and ultimately how well we age. Evidence linking oral bacteria to Alzheimer's disease (AD) is discussed in the context of aging, drawing together data from epidemiological, experimental, genetic, and environmental studies. Immunosenescence results in increased bacterial load as cell-mediated and humoral immune responses wane. The innate immune system gradually takes over; contributing to the rise in circulating proinflammatory cytokines such as TNFα. Maintaining the integrity of the blood-brain barrier (BBB) against a backdrop of increasing bacterial load is important. Aging may favor the proliferation of anaerobes in the mouth eliciting a robust TNFα response from the oral epithelium. Prolonged exposure to high levels of circulating TNFα compromises the integrity of the BBB. Sensitive techniques now detect the "asymptomatic" presence of bacteria in areas previously thought to be sterile, providing new insights into the wider distribution of components of the microbiome. These "immune-tolerated" bacteria may slowly multiply elsewhere until they elicit a chronic inflammatory response; some are now considered causal in instances of atherosclerosis and back pain. Inflammatory processes have long been associated with AD. We propose for a subset of AD patients, aging favors the overgrowth of oral anaerobes established earlier in life provoking a pro-inflammatory innate response that weakens the BBB allowing bacteria to spread and quietly influence the pathogenesis of AD. Finally, we suggest that human polymorphisms considered alongside components of the microbiome may provide new avenues of research for the prevention and treatment of disease.

摘要

本综述汇集了来自不同来源的资料,展示了我们的微生物群如何影响健康以及最终我们的衰老状况。在衰老的背景下讨论了将口腔细菌与阿尔茨海默病(AD)联系起来的证据,综合了流行病学、实验、遗传学和环境研究的数据。免疫衰老导致细胞介导和体液免疫反应减弱时细菌负荷增加。先天性免疫系统逐渐接管;导致循环中的促炎细胞因子如肿瘤坏死因子α(TNFα)增加。在细菌负荷增加的背景下维持血脑屏障(BBB)的完整性很重要。衰老可能有利于口腔中厌氧菌的增殖,引发口腔上皮强烈的TNFα反应。长期暴露于高水平的循环TNFα会损害血脑屏障的完整性。现在,敏感技术可检测到以前认为无菌区域中细菌的“无症状”存在,为微生物群成分的更广泛分布提供了新见解。这些“免疫耐受”细菌可能在其他地方缓慢繁殖,直到引发慢性炎症反应;现在一些细菌被认为是动脉粥样硬化和背痛病例的病因。炎症过程长期以来一直与AD相关。我们提出,对于一部分AD患者,衰老有利于早年在口腔中定植的厌氧菌过度生长,引发促炎先天性反应,削弱血脑屏障,使细菌得以传播并悄悄影响AD的发病机制。最后,我们建议将人类基因多态性与微生物群成分一起考虑,可能为疾病的预防和治疗提供新的研究途径。

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