Multiple sclerosis (MS) is a demyelinating disease of the central nervous system (CNS) characterized by plaques of infiltrating CD4+ and CD8+ T cells. Studies of MS and experimental autoimmune encephalomyelitis (EAE), an animal model of MS, focus on the contribution of CD4+ myelin-specific T cells. The role of CD8+ myelin-specific T cells in mediating EAE or MS has not been described previously. Here, we demonstrate that myelin-specific CD8+ T cells induce severe CNS autoimmunity in mice. The pathology and clinical symptoms in CD8+ T cell–mediated CNS autoimmunity demonstrate similarities to MS not seen in myelin-specific CD4+ T cell–mediated EAE. These data suggest that myelin-specific CD8+ T cells could function as effector cells in the pathogenesis of MS.
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3 September 2001
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September 04 2001
A Pathogenic Role for Myelin-Specific Cd8+ T Cells in a Model for Multiple Sclerosis
Eric S. Huseby,
Eric S. Huseby
aDepartments of Immunology, University of Washington, Seattle, Washington 98195
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Denny Liggitt,
Denny Liggitt
bComparative Medicine, University of Washington, Seattle, Washington 98195
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Thea Brabb,
Thea Brabb
bComparative Medicine, University of Washington, Seattle, Washington 98195
cMolecular Biotechnology, University of Washington, Seattle, Washington 98195
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Bryan Schnabel,
Bryan Schnabel
cMolecular Biotechnology, University of Washington, Seattle, Washington 98195
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Claes Öhlén,
Claes Öhlén
aDepartments of Immunology, University of Washington, Seattle, Washington 98195
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Joan Goverman
Joan Goverman
aDepartments of Immunology, University of Washington, Seattle, Washington 98195
cMolecular Biotechnology, University of Washington, Seattle, Washington 98195
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Eric S. Huseby
aDepartments of Immunology, University of Washington, Seattle, Washington 98195
Denny Liggitt
bComparative Medicine, University of Washington, Seattle, Washington 98195
Thea Brabb
bComparative Medicine, University of Washington, Seattle, Washington 98195
cMolecular Biotechnology, University of Washington, Seattle, Washington 98195
Bryan Schnabel
cMolecular Biotechnology, University of Washington, Seattle, Washington 98195
Claes Öhlén
aDepartments of Immunology, University of Washington, Seattle, Washington 98195
Joan Goverman
aDepartments of Immunology, University of Washington, Seattle, Washington 98195
cMolecular Biotechnology, University of Washington, Seattle, Washington 98195
E.S. Huseby's current address is Howard Hughes Medical Institute, Dept. of Immunology, National Jewish Medical Center, 1400 Jackson St., Denver, CO 80206.
Abbreviations used in this paper: CNS, central nervous system; EAE, experimental autoimmune encephalomyelitis; H&E, hematoxylin and eosin; LFB, Luxol Fast Blue; MBP, myelin basic protein; MBP–CTL, CD8+ T cells specific for MBP; MS, multiple sclerosis; Vac–CTL, Vaccinia-specific CTLs.
Received:
February 09 2001
Revision Requested:
April 20 2001
Accepted:
June 12 2001
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 2001 The Rockefeller University Press
2001
The Rockefeller University Press
J Exp Med (2001) 194 (5): 669–676.
Article history
Received:
February 09 2001
Revision Requested:
April 20 2001
Accepted:
June 12 2001
Citation
Eric S. Huseby, Denny Liggitt, Thea Brabb, Bryan Schnabel, Claes Öhlén, Joan Goverman; A Pathogenic Role for Myelin-Specific Cd8+ T Cells in a Model for Multiple Sclerosis. J Exp Med 3 September 2001; 194 (5): 669–676. doi: https://doi.org/10.1084/jem.194.5.669
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