生物材料在退行性疾病中的作用

Seyed-Amirabbas Ahadiat, Z. Hosseinian
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引用次数: 5

摘要

根据证据,神经免疫激活在中风和帕金森病等神经系统疾病中起着至关重要的作用(1)。明确免疫是正确研究神经免疫激活的第一步(2)。免疫系统是一个复杂的信息处理系统,保护身体免受传染病和过敏原的侵害,并维持体内平衡(3)。存在两种类型的免疫:先天和适应性。适应性免疫是特异性的,由抗体和细胞组成,而先天免疫是非特异性的,反应迅速,包括物理因子和化学成分,如细胞因子和炎症细胞(T淋巴细胞和B淋巴细胞)。通常,先天免疫系统和适应性免疫系统协同作用来入侵病原体(4)。过去,中枢神经系统(CNS)通常被视为免疫系统在正常情况下无法存在的独特器官。近年来,神经免疫信号已被确定为记忆、情感和认知的最重要机制之一。在生理和病理条件下,中枢神经系统参与免疫过程,由于先天免疫细胞驻留在中枢神经系统和外周免疫细胞侵入大脑,大脑是一个高度免疫活跃的器官(5)。神经炎症目前被认为是几乎所有神经退行性疾病的一个重要因素。小胶质细胞是大脑抵御病原体、创伤性脑损伤(TBI)和其他压力的第一道防线,它们在神经炎症中的作用至关重要(6)。大脑中的神经免疫反应通常是先天免疫的结果。相反,适应性免疫系统,如t细胞,在疾病期间是优化神经活动、记忆和大脑细胞因子释放所必需的(7)。尽管如此,疾病和创伤被证明是激活神经免疫系统的刺激。在稳态基线下,神经免疫信号与神经元相互作用,调节神经功能和突触可塑性(8)。在神经免疫激活过程中,病理条件激活内皮细胞、小胶质细胞和星形胶质细胞,这些细胞产生细胞因子和趋化因子(9)。因此,免疫机制在免疫细胞不进入受损组织的情况下运作(10)。中枢神经系统疾病,如神经退行性疾病,与神经胶质活化、细胞迁移、抗原表达和细胞因子释放有关。简而言之,当小胶质细胞被激活或免疫分子,特别是细胞因子和趋化因子过度表达时,就会发生神经免疫激活(11)。鉴于免疫系统在神经退行性疾病中的作用,针对大脑内的免疫反应可能是治疗这些疾病的一种很有希望的方法。因此,与先天免疫系统的免疫成分相互作用的生物材料,包括细胞因子、趋化因子、补体、神经胶质细胞和星形胶质细胞,具有治疗神经退行性疾病的潜力(12,13)。生物材料在再生医学中的应用已变得越来越重要,不仅对研究疾病的发病机制,而且对控制治疗药物到给定部位的输送。因此,它们被广泛用于治疗神经系统疾病和/或改善中枢神经系统的功能恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of biomaterials in degenerative diseases
Dear Editor, According to the evidence, neuroimmune activation plays a crucial role in neurological disorders such as stroke and Parkinson’s disease (1). Clarifying immunity is the initial step in properly investigating neuroimmune activation (2). The immune system is a complex information processing system that protects the body against infectious diseases and allergens and maintains homeostasis (3). Two types of immunity exist: innate and adaptive. Adaptive immunity is specific and consists of antibodies and cells, whereas innate immunity is non-specific, has a rapid response, and includes physical agents and chemical components such as cytokines and inflammatory cells (T and B lymphocytes). Typically, innate and adaptive immune systems work in tandem to invade pathogens (4). In the past, the central nervous system (CNS) was commonly viewed as an immunologically unique organ in which the immune system could not exist under normal circumstances. Neuroimmune signaling has recently been identified as one of the most important mechanisms underlying memory, emotion, and cognition. The CNS is involved in immunological processes under physiological and pathological conditions, and the brain is a highly immunologically active organ due to innate immune cells residing in the CNS and peripheral immune cells invading the brain (5). Neuroinflammation is currently recognized as a significant factor in almost all neurodegenerative disorders. Microglia are the first line of defense in the brain against pathogens, traumatic brain injury (TBI), and other stresses, and their role in neuroinflammation is crucial (6). Neuroimmune responses in the brain are typically the results of innate immunity. In contrast, the adaptive immune system, such as T-cells, is required for optimal neural activity, memory, and cytokine release in the brain during illness (7). Nonetheless, illness and trauma are evidenced as stimuli that activate the neuroimmune systems. In the homeostatic baseline, neuroimmune signaling interacts with neurons and regulates the neural function and synaptic plasticity (8). During neuroimmune activation, pathological conditions activate endothelial cells, microglia, and astrocytes, which produce cytokines and chemokines (9). As a result, the immune mechanism operates without immune cells entering damaged tissue (10). CNS diseases, such as neurodegenerative disorders, are linked to glial activation, cell migration, antigen expression, and cytokine release. Briefly, neuroimmune activation occurs when microglia are activated or immune molecules, particularly cytokines and chemokines, are overexpressed (11). Given the role of the immune system in neurodegenerative diseases, targeting immune reactions within the brain may hold great promise as a treatment for these conditions. Consequently, biomaterials that interact with the immune components of the innate immune system, including cytokines, chemokines, complement, neuroglia cells, and astrocytes, have the potential to treat neurodegenerative disorders (12,13). The use of biomaterials in regenerative medicine has become increasingly important not only for studying disease pathogenesis but also for controlling the delivery of therapeutic drugs to a given site. Therefore, they are widely used to treat neurological disorders and/or improve functional recovery in the CNS.
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