Brain-immune interactions: implication for cognitive impairments in Alzheimer's disease and autoimmune disorders.

IF 3.6 3区 医学 Q3 CELL BIOLOGY
Rashmi Kadam, Muskan Gupta, Orly Lazarov, Bellur S Prabhakar
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引用次数: 0

Abstract

Progressive memory loss and cognitive dysfunction, encompassing deficits in learning, memory, problem solving, spatial reasoning, and verbal expression, are characteristics of Alzheimer's disease and related dementia. A wealth of studies has described multiple roles of the immune system in the development or exacerbation of dementia. Individuals with autoimmune disorders can also develop cognitive dysfunction, a phenomenon termed "autoimmune dementia." Together, these findings underscore the pivotal role of the neuroimmune axis in both Alzheimer's disease and related dementia and autoimmune dementia. The dynamic interplay between adaptive and innate immunity, both in and outside the brain, significantly affects the etiology and progression of these conditions. Multidisciplinary research shows that cognitive dysfunction arises from a bidirectional relationship between the nervous and immune systems, though the specific mechanisms that drive cognitive impairments are not fully understood. Intriguingly, this reciprocal regulation occurs at multiple levels, where neuronal signals can modulate immune responses, and immune system-related processes can influence neuronal viability and function. In this review, we consider the implications of autoimmune responses in various autoimmune disorders and Alzheimer's disease and explore their effects on brain function. We also discuss the diverse cellular and molecular crosstalk between the brain and the immune system, as they may shed light on potential triggers of peripheral inflammation, their effect on the integrity of the blood-brain barrier, and brain function. Additionally, we assess challenges and possibilities associated with developing immune-based therapies for the treatment of cognitive decline.

大脑与免疫的相互作用:对阿尔茨海默病和自身免疫性疾病认知障碍的影响。
渐进性记忆丧失和认知功能障碍,包括学习、记忆、解决问题、空间推理和语言表达等方面的缺陷,是阿尔茨海默病和相关痴呆症(ADRD)的特征。大量研究表明,免疫系统在痴呆症的发生或加重过程中扮演着多重角色。自身免疫性疾病患者也会出现认知功能障碍,这种现象被称为自身免疫性痴呆。这些发现共同强调了神经免疫轴在 ADRD 和自身免疫性痴呆症中的关键作用。大脑内外的适应性免疫和先天性免疫之间的动态相互作用,对这些疾病的病因和进展产生了重大影响。多学科研究表明,认知功能障碍源于神经系统和免疫系统之间的双向关系,但驱动认知障碍的具体机制尚不完全清楚。有趣的是,这种相互调节发生在多个层面,神经元信号可以调节免疫反应,而与免疫系统相关的过程可以影响神经元的活力和功能。在这篇综述中,我们探讨了自身免疫反应在各种自身免疫性疾病和阿尔茨海默病中的影响,并探讨了它们对大脑功能的影响。我们还讨论了大脑与免疫系统之间多种多样的细胞和分子交叉对话,因为它们可能会揭示外周炎症的潜在诱因及其对血脑屏障(BBB)完整性和大脑功能的影响。此外,我们还评估了开发用于治疗认知功能衰退的免疫疗法所面临的挑战和可能性。
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来源期刊
Journal of Leukocyte Biology
Journal of Leukocyte Biology 医学-免疫学
CiteScore
11.50
自引率
0.00%
发文量
358
审稿时长
2 months
期刊介绍: JLB is a peer-reviewed, academic journal published by the Society for Leukocyte Biology for its members and the community of immunobiologists. The journal publishes papers devoted to the exploration of the cellular and molecular biology of granulocytes, mononuclear phagocytes, lymphocytes, NK cells, and other cells involved in host physiology and defense/resistance against disease. Since all cells in the body can directly or indirectly contribute to the maintenance of the integrity of the organism and restoration of homeostasis through repair, JLB also considers articles involving epithelial, endothelial, fibroblastic, neural, and other somatic cell types participating in host defense. Studies covering pathophysiology, cell development, differentiation and trafficking; fundamental, translational and clinical immunology, inflammation, extracellular mediators and effector molecules; receptors, signal transduction and genes are considered relevant. Research articles and reviews that provide a novel understanding in any of these fields are given priority as well as technical advances related to leukocyte research methods.
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