Leite Amanda de Oliveira Ferreira, Bento Torres Neto João, Dos Reis Renata Rodrigues, Sobral Luciane Lobato, de Souza Aline Cristine Passos, Trévia Nonata, de Oliveira Roseane Borner, Lins Nara Alves de Almeida, Diniz Daniel Guerreiro, Diniz José Antonio Picanço, Vasconcelos Pedro Fernando da Costa, Anthony Daniel Clive, Brites Dora, Picanço Diniz Cristovam Wanderley
Laboratório de Investigações em Neurodegeneração e Infecção, Hospital Universitário João de Barros Barreto, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, Brazil.
Laboratório de Microscopia Eletrônica, Instituto Evandro Chagas, Belém, Brazil.
Front Cell Neurosci. 2021 Oct 22;15:749595. doi: 10.3389/fncel.2021.749595. eCollection 2021.
The COVID-19 pandemic imposed a series of behavioral changes that resulted in increased social isolation and a more sedentary life for many across all age groups, but, above all, for the elderly population who are the most vulnerable to infections and chronic neurodegenerative diseases. Systemic inflammatory responses are known to accelerate neurodegenerative disease progression, which leads to permanent damage, loss of brain function, and the loss of autonomy for many aged people. During the COVID-19 pandemic, a spectrum of inflammatory responses was generated in affected individuals, and it is expected that the elderly patients with chronic neurodegenerative diseases who survived SARSCoV-2 infection, it will be found, sooner or later, that there is a worsening of their neurodegenerative conditions. Using mouse prion disease as a model for chronic neurodegeneration, we review the effects of social isolation, sedentary living, and viral infection on the disease progression with a focus on sickness behavior and on the responses of microglia and astrocytes. Focusing on aging, we discuss the cellular and molecular mechanisms related to immunosenescence in chronic neurodegenerative diseases and how infections may accelerate their progression.
新冠疫情带来了一系列行为变化,导致所有年龄段的许多人社交隔离增加,生活更加 sedentary(久坐不动),但最重要的是,对于最易感染和患慢性神经退行性疾病的老年人群体而言。已知全身炎症反应会加速神经退行性疾病的进展,这会导致永久性损伤、脑功能丧失以及许多老年人失去自主能力。在新冠疫情期间,受影响个体产生了一系列炎症反应,预计在感染 SARS-CoV-2 后存活下来的患有慢性神经退行性疾病的老年患者,迟早会发现其神经退行性状况恶化。我们以小鼠朊病毒病作为慢性神经退行性变的模型,回顾社交隔离、久坐不动的生活方式和病毒感染对疾病进展的影响,重点关注疾病行为以及小胶质细胞和星形胶质细胞的反应。着眼于衰老,我们讨论慢性神经退行性疾病中与免疫衰老相关的细胞和分子机制,以及感染如何加速其进展。