The impact of systemic infection on the progression of neurodegenerative disease
The impact of systemic infection on the progression of neurodegenerative disease
In multiple sclerosis — the archetypal inflammatory response in the central nervous system — T cells and macrophages invade the brain and damage the myelin and neurons. In other chronic neurodegenerative diseases, there is an atypical inflammatory response that is characterized by large numbers of activated microglia. These macrophages are primed by components of the neuropathology but might be further activated by systemic infection, which in turn has pronounced effects on inflammation in the brain and perhaps on neurological function. There is emerging evidence to support the idea that nonspecific systemic infection or inflammation in people with existing inflammation in the brain contributes to the rate of disease progression through further activation of these already primed macrophages.
103-112
Perry, V.H.
8f29d36a-8e1f-4082-8700-09483bbaeae4
Newman, T.A.
322290cb-2e9c-445d-a047-00b1bea39a25
Cunningham, C.
6d675038-a4b1-46e2-9e4b-0a5ac27ea2b2
February 2003
Perry, V.H.
8f29d36a-8e1f-4082-8700-09483bbaeae4
Newman, T.A.
322290cb-2e9c-445d-a047-00b1bea39a25
Cunningham, C.
6d675038-a4b1-46e2-9e4b-0a5ac27ea2b2
Perry, V.H., Newman, T.A. and Cunningham, C.
(2003)
The impact of systemic infection on the progression of neurodegenerative disease.
Nature Reviews Neuroscience, 4 (2), .
(doi:10.1038/nrn1032).
Abstract
In multiple sclerosis — the archetypal inflammatory response in the central nervous system — T cells and macrophages invade the brain and damage the myelin and neurons. In other chronic neurodegenerative diseases, there is an atypical inflammatory response that is characterized by large numbers of activated microglia. These macrophages are primed by components of the neuropathology but might be further activated by systemic infection, which in turn has pronounced effects on inflammation in the brain and perhaps on neurological function. There is emerging evidence to support the idea that nonspecific systemic infection or inflammation in people with existing inflammation in the brain contributes to the rate of disease progression through further activation of these already primed macrophages.
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Published date: February 2003
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Local EPrints ID: 56118
URI: http://eprints.soton.ac.uk/id/eprint/56118
ISSN: 1471-0048
PURE UUID: 7fec12cd-cd70-425b-9d50-4c3e0530ee30
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Date deposited: 08 Aug 2008
Last modified: 16 Mar 2024 02:52
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C. Cunningham
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