Abstract
Multiple sclerosis (MS) is widely accepted as an autoimmune disease with myelin basic protein (MBP) a candidate autoantigen. In the current report, human T cell lines specific for an immunodominant region of MBP were shown to have a functional phenotype similar to T helper 1 (Th1) inflammatory cells of the mouse on the basis of their antigen-specific cytotoxic activity and production of interferon-gamma and lymphotoxin/tumor necrosis factor-alpha, but not interleukin-4. In experimental allergic encephalo-myelitis (EAE), a proposed animal model for MS, MBP-specific T cell lines which mediate disease are of the Th1 subtype. Thus, MBP-specific T cells in humans exist which are phenotypically similar to MBP-specific encephalitogenic T cells in murine EAE.
Original language | English (US) |
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Pages (from-to) | 137-143 |
Number of pages | 7 |
Journal | Autoimmunity |
Volume | 15 |
Issue number | 2 |
DOIs | |
State | Published - 1993 |
Externally published | Yes |
Keywords
- Cytotoxic T lymphocyte
- Interferon-gamma
- Lymphotoxin
- Multiple sclerosis
- Myelin basic protein
- T helper 1 lymphocyte
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology