Abstract |
The expression of chemokine receptors on lymphocytes in the blood and CSF of multiple sclerosis (MS) patients was analyzed at relapse and remission. Both CD4+ and CD8+ cells in CSF at relapse were enriched for Th1-type receptors CXCR3 and CCR5 expression, and were reduced for Th2-type receptors CCR3 and CCR4 expression compared with those of the blood. CCR1 and CCR2 expressions on T cells were increased in CSF and blood, respectively. At remission, CCR5 expression, but not CXCR3 expression, was reduced in CSF CD4+ cells. A biased Th1/Th2 balance may play a critical role in active inflammation and CCR5 on CSF CD4+ cells is a good marker of the disease activity.
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Authors | T Misu, H Onodera, K Fujihara, K Matsushima, O Yoshie, N Okita, S Takase, Y Itoyama |
Journal | Journal of neuroimmunology
(J Neuroimmunol)
Vol. 114
Issue 1-2
Pg. 207-12
(Mar 01 2001)
ISSN: 0165-5728 [Print] Netherlands |
PMID | 11240033
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Biomarkers
- CCR1 protein, human
- CCR2 protein, human
- CCR4 protein, human
- CXCR3 protein, human
- Receptors, CCR1
- Receptors, CCR2
- Receptors, CCR4
- Receptors, CCR5
- Receptors, CXCR3
- Receptors, Chemokine
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Topics |
- Adult
- Biomarkers
- CD4-Positive T-Lymphocytes
(immunology, metabolism)
- CD8-Positive T-Lymphocytes
(immunology, metabolism)
- Female
- Humans
- Male
- Multiple Sclerosis, Relapsing-Remitting
(blood, cerebrospinal fluid, immunology)
- Receptors, CCR1
- Receptors, CCR2
- Receptors, CCR4
- Receptors, CCR5
(immunology, metabolism)
- Receptors, CXCR3
- Receptors, Chemokine
(immunology, metabolism)
- Recurrence
- Remission, Spontaneous
- Signal Transduction
(immunology)
- Th1 Cells
(immunology, metabolism)
- Th2 Cells
(immunology, metabolism)
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