Abstract |
Relapsing-remitting experimental autoimmune encephalomyelitis (EAE), a multiple sclerosis model, is induced in mice by injection of myelin proteolipid protein (PLP) encephalitogenic peptide, PLP139-151, in adjuvant. In this study, prior to EAE induction, mice were vaccinated with a bacterial plasmid encoding a PLP- ubiquitin fusion (pCMVUPLP). During the relapse phase of EAE, clinical signs, histopathologic changes, in vitro lymphoproliferation to PLP139-151 and interferon-gamma levels were reduced in pCMVUPLP-vaccinated mice, compared to mock-vaccinated mice (controls). Lymphocytes from pCMVUPLP-vaccinated mice produced interleukin-4, a cytokine lacking in controls. Thus, pCMVUPLP vaccination can modulate the relapse after EAE induction.
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Authors | Diethilde J Theil, Jane E Libbey, Fernando Rodriguez, J Lindsay Whitton, Ikuo Tsunoda, Tobias J Derfuss, Robert S Fujinami |
Journal | Journal of neuroimmunology
(J Neuroimmunol)
Vol. 204
Issue 1-2
Pg. 92-100
(Nov 15 2008)
ISSN: 0165-5728 [Print] Netherlands |
PMID | 18706703
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Cytokines
- Histocompatibility Antigens Class I
- Myelin Proteolipid Protein
- Peptide Fragments
- myelin proteolipid protein (139-151)
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Topics |
- Analysis of Variance
- Animals
- Body Weight
- Cell Proliferation
(drug effects)
- Cytokines
(metabolism)
- Disease Models, Animal
- Encephalomyelitis, Autoimmune, Experimental
(chemically induced, immunology, physiopathology, prevention & control)
- Histocompatibility Antigens Class I
(genetics, metabolism)
- Lymphocyte Activation
(drug effects, immunology)
- Mice
- Molecular Sequence Data
- Myelin Proteolipid Protein
(genetics, immunology)
- Peptide Fragments
- Severity of Illness Index
- Signal Transduction
(drug effects, physiology)
- Spinal Cord
(metabolism, pathology)
- T-Lymphocytes
(drug effects, immunology, metabolism)
- Time Factors
- Ubiquitination
(drug effects, physiology)
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