Abstract |
The expression of beta 2-integrins on gammadelta T cells in naïve mice or those with experimental autoimmune encephalomyelitis (EAE) remains poorly characterized. We compared beta 2-integrin expression and cytokine production between gammadelta and alphabeta T cells over the acute course of EAE. We observed that unlike in alphabeta T cells, beta 2-integrin expression on gammadelta T cells increased significantly from baseline, peaked at Day 10, and remained unchanged in the draining lymph nodes or declined in the spleen and CNS by Day 15. In addition, IFN-gamma- and TNF-alpha-producing gammadelta T cells infiltrated the CNS rapidly and produced significantly more of these cytokines than alphabeta T cells throughout the course of EAE. These results suggest unique roles for beta 2-integrins in the trafficking of gammadelta versus alphabeta T cells during EAE and that gammadelta T cells infiltrate the CNS rapidly, producing cytokines, which modulate acute disease.
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Authors | Sherry S Smith, Scott R Barnum |
Journal | Journal of leukocyte biology
(J Leukoc Biol)
Vol. 83
Issue 1
Pg. 71-9
(Jan 2008)
ISSN: 0741-5400 [Print] United States |
PMID | 17928460
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- CD18 Antigens
- Cytokines
- Receptors, Antigen, T-Cell, alpha-beta
- Receptors, Antigen, T-Cell, gamma-delta
- Tumor Necrosis Factor-alpha
- Interferon-gamma
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Topics |
- Animals
- CD18 Antigens
(biosynthesis, immunology)
- Cytokines
(biosynthesis, immunology)
- Disease Models, Animal
- Encephalomyelitis, Autoimmune, Experimental
(immunology, pathology)
- Female
- Interferon-gamma
(biosynthesis)
- Male
- Mice
- Mice, Inbred C57BL
- Receptors, Antigen, T-Cell, alpha-beta
(immunology)
- Receptors, Antigen, T-Cell, gamma-delta
(immunology)
- Spinal Cord
(immunology)
- Spleen
(immunology)
- T-Lymphocyte Subsets
(immunology)
- Tumor Necrosis Factor-alpha
(biosynthesis)
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