Abstract |
Systemic administration of interferon (IFN)-beta has been recently approved for the treatment of relapsing-remitting multiple sclerosis (RRMS). The immunological mechanism by which IFN-beta ameliorates MS is still partially unknown. We measured the number of blood circulating CD4(+), CD4(-), CD8(+), and CD8(-) T cells secreting IFN-gamma and IL-4 in 26 RRMS patients followed for up to 9 months of an alternate day s.c. treatment with 8x16 IU of IFN-beta1b. Compared to pre-treatment values, a significant (P<0.05) reduction of CD4(+), CD4(-), CD8(+) and CD8(-) cells producing IFN-gamma and of CD4(+) and CD4(-) cells producing IL-4 was observed in MS patients. The IFN-beta-associated effect was evident soon after the beginning of the treatment and persisted for the entire follow-up period. We did not observe any effect of IFN-beta treatment on the percentage of IL-4-producing CD8(+) and CD8(-) cells nor in that of natural killer (NK) cells producing IFN-gamma. Our results show that IFN-beta treatment in MS patients induces a profound and persistent down-regulation of the number of circulating T cells secreting IFN-gamma and IL-4 thus suggesting a broader rather than a specific immunomodulatory effect of IFN-beta in MS.
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Authors | R Furlan, A Bergami, R Lang, E Brambilla, D Franciotta, V Martinelli, G Comi, P Panina, G Martino |
Journal | Journal of neuroimmunology
(J Neuroimmunol)
Vol. 111
Issue 1-2
Pg. 86-92
(Nov 01 2000)
ISSN: 0165-5728 [Print] Netherlands |
PMID | 11063825
(Publication Type: Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Adjuvants, Immunologic
- Receptors, IgG
- Interleukin-4
- Interferon-beta
- Interferon-gamma
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Topics |
- Adjuvants, Immunologic
(administration & dosage)
- Adult
- CD8-Positive T-Lymphocytes
(drug effects, immunology, metabolism)
- Female
- Humans
- Interferon-beta
(administration & dosage)
- Interferon-gamma
(biosynthesis, immunology)
- Interleukin-4
(biosynthesis, immunology)
- Killer Cells, Natural
(drug effects, immunology, metabolism)
- Male
- Middle Aged
- Multiple Sclerosis, Relapsing-Remitting
(drug therapy, immunology)
- Receptors, IgG
(analysis)
- T-Lymphocytes, Helper-Inducer
(drug effects, immunology, metabolism)
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