Neurotrophic cross‐talk between the nervous and immune systems: implications for neurological diseases

M Kerschensteiner, C Stadelmann… - Annals of Neurology …, 2003 - Wiley Online Library
M Kerschensteiner, C Stadelmann, G Dechant, H Wekerle, R Hohlfeld
Annals of Neurology: Official Journal of the American Neurological …, 2003Wiley Online Library
Inflammatory reactions in the central nervous system usually are considered detrimental, but
recent evidence suggests that they also can be beneficial and even have neuroprotective
effects. Intriguingly, immune cells can produce various neurotrophic factors of various
molecular families. The concept of “neuroprotective immunity” will have profound
consequences for the pathogenesis and treatment of neuroinflammatory diseases such as
multiple sclerosis. It also will prove important for neurodegenerative disorders, in which …
Abstract
Inflammatory reactions in the central nervous system usually are considered detrimental, but recent evidence suggests that they also can be beneficial and even have neuroprotective effects. Intriguingly, immune cells can produce various neurotrophic factors of various molecular families. The concept of “neuroprotective immunity” will have profound consequences for the pathogenesis and treatment of neuroinflammatory diseases such as multiple sclerosis. It also will prove important for neurodegenerative disorders, in which inflammatory reactions often occur. This review focuses on recent findings that immune cells produce brain‐derived neurotrophic factor in multiple sclerosis lesions, whereas neurons and astrocytes express the appropriate tyrosine kinase receptor TrkB. Together with functional evidence for the neuroprotective effects of immune cells, these observations support the concept of “neuroprotective immunity.” We next examine current and future therapeutic strategies for multiple sclerosis and experimental autoimmune encephalomyelitis in light of neuroprotective immunity and finally address the broader implications of this new concept for other neuroinflammatory and neurodegenerative diseases. Ann Neurol 2003
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