Division of Bacteriology and Parasitology, Tulane National Primate Research Center, Tulane University, 18703 Three Rivers Road, Covington, LA 70433, USA.
Mediators Inflamm. 2013;2013:480739. doi: 10.1155/2013/480739. Epub 2013 Aug 12.
Cytokines and chemokines are proteins that coordinate the immune response throughout the body. The dysregulation of cytokines and chemokines is a central feature in the development of neuroinflammation, neurodegeneration, and demyelination both in the central and peripheral nervous systems and in conditions of neuropathic pain. Pathological states within the nervous system can lead to activation of microglia. The latter may mediate neuronal and glial cell injury and death through production of proinflammatory factors such as cytokines and chemokines. These then help to mobilize the adaptive immune response. Although inflammation may induce beneficial effects such as pathogen clearance and phagocytosis of apoptotic cells, uncontrolled inflammation can result in detrimental outcomes via the production of neurotoxic factors that exacerbate neurodegenerative pathology. In states of prolonged inflammation, continual activation and recruitment of effector cells can establish a feedback loop that perpetuates inflammation and ultimately results in neuronal injury. A critical balance between repair and proinflammatory factors determines the outcome of a neurodegenerative process. This review will focus on how cytokines and chemokines affect neuroinflammation and disease pathogenesis in bacterial meningitis and brain abscesses, Lyme neuroborreliosis, human immunodeficiency virus encephalitis, and neuropathic pain.
细胞因子和趋化因子是协调全身免疫反应的蛋白质。细胞因子和趋化因子的失调是中枢和周围神经系统中神经炎症、神经退行性变和脱髓鞘形成以及神经病理性疼痛发展的一个核心特征。神经系统内的病理状态可导致小胶质细胞的激活。后者可通过产生促炎因子(如细胞因子和趋化因子)来介导神经元和神经胶质细胞的损伤和死亡。这些因子有助于动员适应性免疫反应。尽管炎症可能诱导有益的效果,如病原体清除和凋亡细胞的吞噬作用,但不受控制的炎症可能会通过产生加剧神经退行性病理的神经毒性因子而产生有害的后果。在持续炎症的状态下,效应细胞的持续激活和募集可建立一个反馈回路,使炎症持续存在,最终导致神经元损伤。修复和促炎因子之间的关键平衡决定了神经退行性过程的结果。本综述将重点关注细胞因子和趋化因子如何影响细菌性脑膜炎和脑脓肿、莱姆神经Borreliosis、人类免疫缺陷病毒脑炎和神经病理性疼痛中的神经炎症和疾病发病机制。