Harris Steven A, Harris Elizabeth A
St. Vincent Medical Group, Northside Internal Medicine, Indianapolis, IN, USA.
Indiana University School of Medicine, Indianapolis, IN, USA.
J Alzheimers Dis. 2015;48(2):319-53. doi: 10.3233/JAD-142853.
This review focuses on research in epidemiology, neuropathology, molecular biology, and genetics regarding the hypothesis that pathogens interact with susceptibility genes and are causative in sporadic Alzheimer's disease (AD). Sporadic AD is a complex multifactorial neurodegenerative disease with evidence indicating coexisting multi-pathogen and inflammatory etiologies. There are significant associations between AD and various pathogens, including Herpes simplex virus type 1 (HSV-1), Cytomegalovirus, and other Herpesviridae, Chlamydophila pneumoniae, spirochetes, Helicobacter pylori, and various periodontal pathogens. These pathogens are able to evade destruction by the host immune system, leading to persistent infection. Bacterial and viral DNA and RNA and bacterial ligands increase the expression of pro-inflammatory molecules and activate the innate and adaptive immune systems. Evidence demonstrates that pathogens directly and indirectly induce AD pathology, including amyloid-β (Aβ) accumulation, phosphorylation of tau protein, neuronal injury, and apoptosis. Chronic brain infection with HSV-1, Chlamydophila pneumoniae, and spirochetes results in complex processes that interact to cause a vicious cycle of uncontrolled neuroinflammation and neurodegeneration. Infections such as Cytomegalovirus, Helicobacter pylori, and periodontal pathogens induce production of systemic pro-inflammatory cytokines that may cross the blood-brain barrier to promote neurodegeneration. Pathogen-induced inflammation and central nervous system accumulation of Aβ damages the blood-brain barrier, which contributes to the pathophysiology of AD. Apolipoprotein E4 (ApoE4) enhances brain infiltration by pathogens including HSV-1 and Chlamydophila pneumoniae. ApoE4 is also associated with an increased pro-inflammatory response by the immune system. Potential antimicrobial treatments for AD are discussed, including the rationale for antiviral and antibiotic clinical trials.
本综述聚焦于流行病学、神经病理学、分子生物学和遗传学方面的研究,这些研究围绕病原体与易感性基因相互作用并导致散发性阿尔茨海默病(AD)这一假说展开。散发性AD是一种复杂的多因素神经退行性疾病,有证据表明存在多种病原体和炎症病因并存的情况。AD与多种病原体之间存在显著关联,包括1型单纯疱疹病毒(HSV-1)、巨细胞病毒以及其他疱疹病毒科病毒、肺炎衣原体、螺旋体、幽门螺杆菌和多种牙周病原体。这些病原体能够逃避宿主免疫系统的破坏,导致持续感染。细菌和病毒的DNA和RNA以及细菌配体可增加促炎分子的表达并激活先天性和适应性免疫系统。有证据表明,病原体直接或间接诱导AD病理变化,包括淀粉样β蛋白(Aβ)积累、tau蛋白磷酸化、神经元损伤和细胞凋亡。HSV-1、肺炎衣原体和螺旋体的慢性脑感染会导致复杂的相互作用过程,从而引发不受控制的神经炎症和神经退行性变的恶性循环。巨细胞病毒、幽门螺杆菌和牙周病原体等感染会诱导全身性促炎细胞因子的产生,这些细胞因子可能穿过血脑屏障促进神经退行性变。病原体诱导的炎症和Aβ在中枢神经系统的积累会损害血脑屏障,这对AD的病理生理学有影响。载脂蛋白E4(ApoE4)会增强包括HSV-1和肺炎衣原体在内的病原体对脑的浸润。ApoE4还与免疫系统促炎反应增加有关。本文讨论了AD潜在的抗菌治疗方法,包括抗病毒和抗生素临床试验的原理。