IFN-β differentially regulates the function of T cell subsets in MS and EAE. (August 2016)
- Record Type:
- Journal Article
- Title:
- IFN-β differentially regulates the function of T cell subsets in MS and EAE. (August 2016)
- Main Title:
- IFN-β differentially regulates the function of T cell subsets in MS and EAE
- Authors:
- Kavrochorianou, Nadia
Markogiannaki, Melina
Haralambous, Sylva - Abstract:
- Highlights: T cell targeting therapies in MS act either directly or indirectly. Endogenous and exogenous IFN-β regulate pro- and anti-inflammatory responses. IFN-β differentially affects T cell subsets involved in MS and EAE. Homeostatic functions of IFN-β are disease staging and setting context-dependent. Abstract: Multiple sclerosis (MS) is considered as a T cell mediated autoimmune disease of the CNS, although a pathogenic role has also been attributed to other immune cell types as well as to environmental and genetic factors. Considering that T cells are interesting from an immunopathogenic point of view and consequently from a therapeutic perspective, various T cell targeted therapies have been approved for MS. Interferon beta (IFN-β) is widely used as first-line intervention for modulating T cell responses, although its pleiotropic and multifaceted activities influence its effectiveness on the disease development, with mechanisms that are not yet fully understood. Since different T cell populations, including pro-inflammatory and regulatory T cells, might affect the course of MS, the effects of IFN-β become even more complex. This review will summarize recent findings regarding the T cell targeted effect of IFN-β in MS and its animal model EAE, with emphasis on the direct actions of endogenous and exogenous IFN-β on each T cell subpopulation involved in CNS autoimmunity. Delineating how IFN-β exerts its action on different T cell types may eventually contribute to theHighlights: T cell targeting therapies in MS act either directly or indirectly. Endogenous and exogenous IFN-β regulate pro- and anti-inflammatory responses. IFN-β differentially affects T cell subsets involved in MS and EAE. Homeostatic functions of IFN-β are disease staging and setting context-dependent. Abstract: Multiple sclerosis (MS) is considered as a T cell mediated autoimmune disease of the CNS, although a pathogenic role has also been attributed to other immune cell types as well as to environmental and genetic factors. Considering that T cells are interesting from an immunopathogenic point of view and consequently from a therapeutic perspective, various T cell targeted therapies have been approved for MS. Interferon beta (IFN-β) is widely used as first-line intervention for modulating T cell responses, although its pleiotropic and multifaceted activities influence its effectiveness on the disease development, with mechanisms that are not yet fully understood. Since different T cell populations, including pro-inflammatory and regulatory T cells, might affect the course of MS, the effects of IFN-β become even more complex. This review will summarize recent findings regarding the T cell targeted effect of IFN-β in MS and its animal model EAE, with emphasis on the direct actions of endogenous and exogenous IFN-β on each T cell subpopulation involved in CNS autoimmunity. Delineating how IFN-β exerts its action on different T cell types may eventually contribute to the designing of therapeutic strategies aiming to improve the effectiveness of this drug for MS treatment. … (more)
- Is Part Of:
- Cytokine & growth factor reviews. Volume 30(2016)
- Journal:
- Cytokine & growth factor reviews
- Issue:
- Volume 30(2016)
- Issue Display:
- Volume 30, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 30
- Issue:
- 2016
- Issue Sort Value:
- 2016-0030-2016-0000
- Page Start:
- 47
- Page End:
- 54
- Publication Date:
- 2016-08
- Subjects:
- APC antigen-presenting cell -- BBB blood-brain barrier -- CCR C-C chemokine receptor -- CNS central nervous system -- CSF cerebrospinal fluid -- CXCR C-X-C chemokine receptor -- EAE experimental autoimmune encephalomyelitis -- FoxA forkhead box protein A -- FOXP3 forkhead box P3 -- GITRL glucocorticoid-induced TNF receptor-related protein -- IFN interferon -- IFNAR interferon receptor -- IL interleukin -- IRF interferon regulatory factor -- LN lymph nodes -- MBP myelin basic protein -- MIP macrophage inflammatory protein -- MMP9 metalloproteinase-9 -- MOG myelin oligodendrocyte glycoprotein -- MS multiple sclerosis -- NAb neutralizing antibody -- NMO neuromyelitis optica -- PAMP pathogen-associated molecular pattern -- PBMC peripheral blood mononuclear cell -- pDC plasmacytoid dendritic cell -- PD-L programmed death-ligand -- PLP proteolipid protein -- PRR pathogen recognition receptor -- SOCS suppressor of cytokine signaling -- STAT signal transducer and activator of transcription -- Tfh T follicular helper cell -- Tfr T follicular regulatory cell -- Th T helper cell -- TNF tumor necrosis factor -- Tr1 type 1 regulatory cells -- Treg T regulatory cell -- USP18 Ubiquitin specific peptidase 18 -- VLA4 very late antigen 4
Multiple sclerosis -- Interferon beta -- T cell subsets -- Inflammation -- Experimental Autoimmune Encephalomyelitis
Cytokines -- Periodicals
571.84 - Journal URLs:
- http://www.sciencedirect.com/science/journal/13596101 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.cytogfr.2016.03.013 ↗
- Languages:
- English
- ISSNs:
- 1359-6101
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3506.778500
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