Babkina Anastasiya S, Yadgarov Mikhail Ya, Lyubomudrov Maxim A, Ostrova Irina V, Volkov Alexey V, Kuzovlev Artem N, Grechko Andrey V, Golubev Arkady M
Federal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, Moscow 107031, Russia.
Department of Pathological Anatomy, Institute of Medicine, Peoples' Friendship University of Russia, Moscow 117198, Russia.
Biomedicines. 2023 May 9;11(5):1407. doi: 10.3390/biomedicines11051407.
Despite the enormous interest in COVID-19, there is no clear understanding of the mechanisms underlying the neurological symptoms in COVID-19. Microglia have been hypothesized to be a potential mediator of the neurological manifestations associated with COVID-19. In most existing studies to date, morphological changes in internal organs, including the brain, are considered in isolation from clinical data and defined as a consequence of COVID-19. We performed histological immunohistochemical (IHC) studies of brain autopsy materials of 18 patients who had died from COVID-19. We evaluated the relationship of microglial changes with the clinical and demographic characteristics of the patients. The results revealed neuronal alterations and circulatory disturbances. We found an inverse correlation between the integral density Iba-1 (microglia/macrophage-specific marker) IHC staining and the duration of the disease (R = -0.81, = 0.001), which may indicate a reduced activity of microglia and do not exclude their damage in the long-term course of COVID-19. The integral density of Iba-1 IHC staining was not associated with other clinical and demographic factors. We observed a significantly higher number of microglial cells in close contact with neurons in female patients, which confirms gender differences in the course of the disease, indicating the need to study the disease from the standpoint of personalized medicine.
尽管对新冠病毒(COVID-19)有着极大的关注,但对于COVID-19神经症状背后的机制仍缺乏清晰的认识。小胶质细胞被认为是与COVID-19相关神经表现的潜在介导者。在迄今为止的大多数现有研究中,包括大脑在内的内脏器官的形态变化是与临床数据分开考虑的,并被定义为COVID-19的结果。我们对18例死于COVID-19患者的脑尸检材料进行了组织学免疫组织化学(IHC)研究。我们评估了小胶质细胞变化与患者临床和人口统计学特征之间的关系。结果显示存在神经元改变和循环系统紊乱。我们发现Iba-1(小胶质细胞/巨噬细胞特异性标志物)免疫组化染色的积分密度与疾病持续时间呈负相关(R = -0.81,P = 0.001),这可能表明小胶质细胞活性降低,并且不排除它们在COVID-19的长期病程中受到损伤。Iba-1免疫组化染色的积分密度与其他临床和人口统计学因素无关。我们观察到女性患者中与神经元紧密接触的小胶质细胞数量明显更多,这证实了疾病过程中的性别差异,表明有必要从个性化医学的角度研究该疾病。