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Increased IL-10 mRNA and IL-23 mRNA expression in multiple sclerosis:
interferon-
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| Abstract |
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Background
Interferon (IFN)-
therapy in multiple sclerosis (MS) has been suggested to
promote a deviation from T lymphocyte production of pathogenic Th1 cytokines to less
detrimental Th2 cytokines, but this is still controversial. We studied patterns of
in vivo blood mononuclear cell (MNC) and whole blood cytokine and
transcription factor mRNA expression before and during IFN-
therapy in MS.
Methods
Twenty patients with relapsing–remitting MS were sampled before and after 3
months of treatment with IFN-
along with 15 healthy volunteers. An
additional 39 patients and 50 healthy volunteers served to confirm initial findings.
mRNA was analyzed by real-time reverse transcriptase polymerase chain reaction
(PCR).
Results
We found elevated expression of interleukin (IL)-23 and IL-10 in untreated MS
patients. IFN-
therapy increased IL-10 and decreased IL-23 expression
independently of any Th1 or Th2 cytokines. The largest changes in cytokine mRNA
levels occurred early (~9–12 h) after an IFN-
injection.
Conclusion
We found no evidence of a Th1- or Th2-mRNA-promoting effect of IFN-
therapy. The therapeutic effect of IFN-
is more likely attributable to the
induction of the regulatory cytokine IL-10. The elevated IL-23 mRNA levels in MS
patients are noteworthy in view of the newly discovered IL-23-driven Th17 T-cell
subset, which is crucial in animal models of MS. Since IFN-
therapy
resulted in decreased IL-23 mRNA levels, the Th17 axis could be another target of
IFN-
therapy.
Key Words:
autoimmune diseases, cytokines, immunotherapy, interferon-
treatment, interleukin-10, interleukin-23, multiple sclerosis
First published on April 18, 2008, doi:10.1177/1352458507087136
Multiple Sclerosis 2008;14:622.
A more recent version of this article appeared on June 1, 2008
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V. S. Ramgolam, Y. Sha, J. Jin, X. Zhang, and S. Markovic-Plese IFN-{beta} Inhibits Human Th17 Cell Differentiation J. Immunol., October 15, 2009; 183(8): 5418 - 5427. [Abstract] [Full Text] [PDF] |
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treatment increases IL-10 mRNA expression while reducing IL-23
mRNA expression
