Cytokines and Chemokines at the Crossroads of Neuroinflammation, Neurodegeneration, and Neuropathic Pain

Цитокины и хемокины на стыке нейровоспаления, нейродегенерации и нейропатической боли
Geeta Ramesh, Andrew G. MacLean, Mario T. Philipp
2013-01-01

cytokines and chemokinesmicroglia activationneurodegenerationneuroinflammationneuropathic pain
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.
1
Activated microglia can promote neuronal and glial injury or death by producing proinflammatory cytokines and chemokines that mobilize adaptive immunity.
2
Dysregulated cytokine and chemokine signaling is central to neuroinflammation, neurodegeneration, demyelination, and neuropathic pain in central and peripheral nervous systems.
3
Inflammation can be beneficial through pathogen clearance and apoptotic-cell phagocytosis, but uncontrolled responses generate neurotoxic factors that worsen neurodegenerative pathology.
4
Prolonged inflammation creates a self-perpetuating feedback loop through continual effector-cell activation and recruitment, ultimately causing neuronal injury.
5
The balance between reparative and proinflammatory factors influences disease outcomes across bacterial meningitis, brain abscesses, Lyme neuroborreliosis, HIV encephalitis, and neuropathic pain.

Cytokines and chemokines in the central and peripheral nervous systems during neuroinflammatory, neurodegenerative, demyelinating, and neuropathic pain conditions

Their dysregulation and effects on microglial activation, inflammatory feedback, neuronal and glial injury, and disease pathogenesis

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2013-01-01
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Geeta Ramesh
Andrew G. MacLean
Mario T. Philipp
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