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是时候在阿尔茨海默病中测试抗菌疗法了。

Time to test antibacterial therapy in Alzheimer's disease.

机构信息

Unit of Epidemiological Research on Aging, National Institute of Gastroenterology 'Saverio de Bellis', Research Hospital, Castellana Grotte, Bari, Italy.

Neurodegenerative Disease Unit, Department of Basic Medicine, Neuroscience, and Sense Organs, University of Bari Aldo Moro, Bari, Italy.

出版信息

Brain. 2019 Oct 1;142(10):2905-2929. doi: 10.1093/brain/awz244.

Abstract

Alzheimer's disease is associated with cerebral accumulation of amyloid-β peptide and hyperphosphorylated tau. In the past 28 years, huge efforts have been made in attempting to treat the disease by reducing brain accumulation of amyloid-β in patients with Alzheimer's disease, with no success. While anti-amyloid-β therapies continue to be tested in prodromal patients with Alzheimer's disease and in subjects at risk of developing Alzheimer's disease, there is an urgent need to provide therapeutic support to patients with established Alzheimer's disease for whom current symptomatic treatment (acetylcholinesterase inhibitors and N-methyl d-aspartate antagonist) provide limited help. The possibility of an infectious aetiology for Alzheimer's disease has been repeatedly postulated over the past three decades. Infiltration of the brain by pathogens may act as a trigger or co-factor for Alzheimer's disease, with Herpes simplex virus type 1, Chlamydia pneumoniae, and Porphyromonas gingivalis being most frequently implicated. These pathogens may directly cross a weakened blood-brain barrier, reach the CNS and cause neurological damage by eliciting neuroinflammation. Alternatively, pathogens may cross a weakened intestinal barrier, reach vascular circulation and then cross blood-brain barrier or cause low grade chronic inflammation and subsequent neuroinflammation from the periphery. The gut microbiota comprises a complex community of microorganisms. Increased permeability of the gut and blood-brain barrier induced by microbiota dysbiosis may impact Alzheimer's disease pathogenesis. Inflammatory microorganisms in gut microbiota are associated with peripheral inflammation and brain amyloid-β deposition in subjects with cognitive impairment. Oral microbiota may also influence Alzheimer's disease risk through circulatory or neural access to the brain. At least two possibilities can be envisaged to explain the association of suspected pathogens and Alzheimer's disease. One is that patients with Alzheimer's disease are particularly prone to microbial infections. The other is that microbial infection is a contributing cause of Alzheimer's disease. Therapeutic trials with antivirals and/or antibacterials could resolve this dilemma. Indeed, antiviral agents are being tested in patients with Alzheimer's disease in double-blind placebo-controlled studies. Although combined antibiotic therapy was found to be effective in animal models of Alzheimer's disease, antibacterial drugs are not being widely investigated in patients with Alzheimer's disease. This is because it is not clear which bacterial populations in the gut of patients with Alzheimer's disease are overexpressed and if safe, selective antibacterials are available for them. On the other hand, a bacterial protease inhibitor targeting P. gingivalis toxins is now being tested in patients with Alzheimer's disease. Clinical studies are needed to test if countering bacterial infection may be beneficial in patients with established Alzheimer's disease.

摘要

阿尔茨海默病与脑内淀粉样β肽和过度磷酸化的 tau 积聚有关。在过去的 28 年中,人们做出了巨大的努力,试图通过减少阿尔茨海默病患者大脑中淀粉样β的积累来治疗这种疾病,但没有成功。虽然抗淀粉样β疗法仍在进行临床试验,用于有阿尔茨海默病前期症状的患者和有患阿尔茨海默病风险的人群,但迫切需要为已确诊的阿尔茨海默病患者提供治疗支持,因为目前的对症治疗(乙酰胆碱酯酶抑制剂和 N-甲基-D-天冬氨酸拮抗剂)提供的帮助有限。过去三十年来,阿尔茨海默病的感染病因学说反复被提出。病原体浸润大脑可能作为阿尔茨海默病的触发因素或协同因素,单纯疱疹病毒 1 型、肺炎衣原体和牙龈卟啉单胞菌最常被牵连。这些病原体可能直接穿过较弱的血脑屏障,到达中枢神经系统,并通过引发神经炎症引起神经损伤。或者,病原体可能穿过较弱的肠道屏障,进入血管循环,然后穿过血脑屏障,或者引起低水平的慢性炎症和来自外周的后续神经炎症。肠道微生物组由复杂的微生物群落组成。肠道和血脑屏障通透性的增加由微生物组失调引起,可能会影响阿尔茨海默病的发病机制。肠道微生物组中的炎症微生物与认知障碍患者的外周炎症和大脑淀粉样β沉积有关。口腔微生物组也可能通过循环或神经途径进入大脑来影响阿尔茨海默病的风险。可以设想至少两种可能性来解释可疑病原体与阿尔茨海默病的关联。一种是阿尔茨海默病患者特别容易受到微生物感染。另一种是微生物感染是阿尔茨海默病的一个促成因素。抗病毒药物和/或抗菌药物的治疗试验可以解决这一困境。事实上,抗病毒药物正在进行临床试验,用于阿尔茨海默病患者的双盲安慰剂对照研究。尽管联合抗生素治疗在阿尔茨海默病动物模型中被证明是有效的,但抗菌药物在阿尔茨海默病患者中并没有得到广泛研究。这是因为目前尚不清楚阿尔茨海默病患者肠道中哪些细菌种群过度表达,以及是否有安全的、选择性的抗菌药物可供使用。另一方面,一种针对牙龈卟啉单胞菌毒素的细菌蛋白酶抑制剂目前正在进行临床试验,用于阿尔茨海默病患者。需要进行临床试验来测试对抗细菌感染是否对已确诊的阿尔茨海默病患者有益。

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