Lin Chih-Chung 'Jerry', Tian Yuyao, Tanzi Rudolph E, Jorfi Mehdi
Genetics and Aging Research Unit, McCance Center for Brain Health, Mass General Institute for Neurodegenerative Disease, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, USA.
Genetics and Aging Research Unit, McCance Center for Brain Health, Mass General Institute for Neurodegenerative Disease, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, USA.
Trends Immunol. 2024 Dec;45(12):971-986. doi: 10.1016/j.it.2024.10.002. Epub 2024 Nov 12.
Peripheral immune cells play an important role in the pathology of Alzheimer's disease (AD), impacting processes such as amyloid and tau protein aggregation, glial activation, neuronal integrity, and cognitive decline. Here, we examine cutting-edge strategies - encompassing animal and cellular models - used to investigate the roles of peripheral immune cells in AD. Approaches such as antibody-mediated depletion, genetic ablation, and bone marrow chimeras in mouse models have been instrumental in uncovering T, B, and innate immune cell disease-modifying functions. However, challenges such as specificity, off-target effects, and differences between human and mouse immune systems underscore the need for more human-relevant models. Emerging multicellular models replicating critical aspects of human brain tissue and neuroimmune interactions increasingly offer fresh insights into the role of immune cells in AD pathogenesis. Refining these methodologies can deepen our understanding of immune cell contributions to AD and support the development of novel immune-related therapeutic interventions.
外周免疫细胞在阿尔茨海默病(AD)的病理过程中发挥着重要作用,影响着淀粉样蛋白和tau蛋白聚集、胶质细胞活化、神经元完整性和认知衰退等过程。在此,我们研究了用于探究外周免疫细胞在AD中作用的前沿策略,包括动物和细胞模型。诸如抗体介导的清除、基因消融以及小鼠模型中的骨髓嵌合体等方法,对于揭示T细胞、B细胞和固有免疫细胞的疾病修饰功能起到了重要作用。然而,特异性、脱靶效应以及人类和小鼠免疫系统之间的差异等挑战,凸显了对更具人类相关性模型的需求。新兴的多细胞模型复制了人类脑组织和神经免疫相互作用的关键方面,越来越多地为免疫细胞在AD发病机制中的作用提供了新的见解。完善这些方法可以加深我们对免疫细胞在AD中作用的理解,并支持新型免疫相关治疗干预措施的开发。