A revised view of the central nervous system microenvironment and major histocompatibility complex class II antigen presentation
A revised view of the central nervous system microenvironment and major histocompatibility complex class II antigen presentation
There are numerous observations reporting that phagocytes expressing major histocompatibility complex (MHC) Class II molecules are associated with the central nervous system (CNS) in normal and pathological conditions. Although MHC Class II expression is necessary for antigen presentation to CD4 + T-cells, it is not sufficient and co-stimulatory molecules are also required. We review here recent in vivo studies demonstrating that the microglia and perivascular macrophages are unable to initiate a primary immune response in the CNS microenvironment, but may support secondary immune responses. Although in vitro studies show that microgila do not support a primary immune response leading to T-cell proliferation, they do show that microglia may protect the CNS from the unwanted attentions of autoreactive T- cells by inducing their apoptosis. The lack of cells in the CNS parenchyma with the ability to initiate a primary immune response has a cost, namely that pathogens may persist in the CNS undetected by the immune system.
Central nervous system, MHC class II, T-cell
113-121
Hugh Perry, V.
8f29d36a-8e1f-4082-8700-09483bbaeae4
1 October 1998
Hugh Perry, V.
8f29d36a-8e1f-4082-8700-09483bbaeae4
Hugh Perry, V.
(1998)
A revised view of the central nervous system microenvironment and major histocompatibility complex class II antigen presentation.
Journal of Neuroimmunology, 90 (2), .
(doi:10.1016/S0165-5728(98)00145-3).
Abstract
There are numerous observations reporting that phagocytes expressing major histocompatibility complex (MHC) Class II molecules are associated with the central nervous system (CNS) in normal and pathological conditions. Although MHC Class II expression is necessary for antigen presentation to CD4 + T-cells, it is not sufficient and co-stimulatory molecules are also required. We review here recent in vivo studies demonstrating that the microglia and perivascular macrophages are unable to initiate a primary immune response in the CNS microenvironment, but may support secondary immune responses. Although in vitro studies show that microgila do not support a primary immune response leading to T-cell proliferation, they do show that microglia may protect the CNS from the unwanted attentions of autoreactive T- cells by inducing their apoptosis. The lack of cells in the CNS parenchyma with the ability to initiate a primary immune response has a cost, namely that pathogens may persist in the CNS undetected by the immune system.
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Accepted/In Press date: 26 May 1998
Published date: 1 October 1998
Keywords:
Central nervous system, MHC class II, T-cell
Identifiers
Local EPrints ID: 489607
URI: http://eprints.soton.ac.uk/id/eprint/489607
ISSN: 0165-5728
PURE UUID: 74efc658-2596-42b0-aced-37296605caa6
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Date deposited: 29 Apr 2024 16:46
Last modified: 29 Apr 2024 16:46
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