Treatment of mice with the suppressor of cytokine signaling-1 mimetic peptide, tyrosine kinase inhibitor peptide, prevents development of the acute form of …

MG Mujtaba, LO Flowers, CB Patel… - The Journal of …, 2005 - journals.aai.org
MG Mujtaba, LO Flowers, CB Patel, RA Patel, MI Haider, HM Johnson
The Journal of Immunology, 2005journals.aai.org
We have previously characterized a novel tyrosine kinase inhibitor peptide (Tkip) that is a
mimetic of suppressor of cytokine signaling 1 (SOCS-1) and inhibits JAK2 phosphorylation
of the transcription factor STAT1α. We show in this study that Tkip protects mice against
experimental allergic encephalomyelitis (EAE), an animal model for multiple sclerosis. Mice
are immunized with myelin basic protein (MBP) for induction of disease. Tkip (63 μg)
administered every other day suppressed the development of acute EAE in 75% of New …
Abstract
We have previously characterized a novel tyrosine kinase inhibitor peptide (Tkip) that is a mimetic of suppressor of cytokine signaling 1 (SOCS-1) and inhibits JAK2 phosphorylation of the transcription factor STAT1α. We show in this study that Tkip protects mice against experimental allergic encephalomyelitis (EAE), an animal model for multiple sclerosis. Mice are immunized with myelin basic protein (MBP) for induction of disease. Tkip (63 μg) administered every other day suppressed the development of acute EAE in 75% of New Zealand White (NZW) mice. Furthermore, Tkip completely protected SJL/J mice, which where induced to get the relapsing/remitting form of EAE, against relapses compared with control groups in which> 70% of the mice relapsed after primary incidence of disease. Protection of mice by Tkip was similar to that seen with the type I IFN, IFN-τ. Protection of mice correlated with lower MBP Ab titers in Tkip-treated groups as well as suppression of MBP-induced proliferation of splenocytes taken from EAE-afflicted mice. Cessation of Tkip and IFN-τ administration resulted in SJL/J mice relapsing back into disease. Prolonged treatment of mice with Tkip produced no evidence of cellular toxicity or weight loss. Consistent with its JAK2 inhibitory function, Tkip also inhibited the activity of the inflammatory cytokine TNF-α, which uses the STAT1α transcription factor. The data presented in this study show that Tkip, like the type I IFN, IFN-τ, inhibits both the autoreactive cellular and humoral responses in EAE and ameliorates both the acute and chronic relapsing/remitting forms of EAE.
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