Use of cell-permeable peptide inhibitors of the JNK signal transduction pathway for the treatment of chronic or non-chronic inflammatory eye diseases
The present invention refers to the use of protein kinase inhibitors and more specifically to the use of inhibitors of the protein kinase c-Jun amino terminal kinase, JNK inhibitor (poly-)peptides, chimeric peptides, or of nucleic acids encoding same as well as pharmaceutical compositions containing same, for the treatment of non-chronic or chronic inflammatory eye diseases, such as inflammatory diseases of the blephara, conjunctiva, cornea, sclera, the vitreous body, uvea, ciliary body, choroid, orbital bone, lacrimal gland, or iris, in particular wherein the inflammatory disease is selected from hordeolum, chalazion, conjunktivitis, keratitis, scleritis, episcleritis, endophthalmitis, panophtalmitis, irititis, uveitis, cyclitis, chorioiditis, orbital phlegmon, and myositis of the eye muscle etc.
1. A method of treating anterior uveitis in a subject in need of treatment thereof, the method comprising administering to the subject a pharmaceutical composition, the pharmaceutical composition comprising a polypeptide having at least 90% sequence identity to SEQ ID NO: 11, wherein the polypeptide comprises a first domain that specifically binds to a c-jun amino terminal kinase (JNK) to inhibit JNK activity, and a second domain, which is covalently linked to the first domain and augments cellular uptake of the peptide and augments nuclear localization of the peptide within the cell.
2. The method of claim 1 , wherein the first domain of the polypeptide sequence comprises SEQ ID NO: 2.
3. The method of claim 1 , wherein the second domain of the polypeptide comprises SEQ ID NO: 6.
4. The method of claim 1 , wherein the polypeptide comprises SEQ ID NO: 11.
5. The method of claim 1 , wherein the pharmaceutical composition is administered by a route selected from the group consisting of intravenous, intramuscular, subcutaneous, intradermal, transdermal, oral, rectal, nasal, intranasal, epidermal and topical.
6. The method of claim 1 , wherein the pharmaceutical composition delivers the peptide to the subject in a dose (per kg bodyweight) selected from the group consisting of from about 1 pmol/kg to about 1 mmol/kg, from about 10 pmol/kg to about 0.1 mmol/kg, from about 10 pmol/kg to about 0.01 mmol/kg, from about 50 pmol/kg to about 1 pmol/kg, from about 100 pmol/kg to about 500 nmol/kg, from about 200 pmol/kg to about 300 nmol/kg, from about 300 pmol/kg to about 100 nmol/kg, from about 500 pmol/kg to about 50 nmol/kg, from about 750 pmol/kg to about 30 nmol/kg, from about 250 pmol/kg to about 5 nmol/kg and from about 1 nmol/kg to about 10 nmol/kg.
7. The method of claim 1 , wherein the polypeptide consists of SEQ ID NO: 11.
8. The method of claim 1 , wherein the anterior uveitis is chronic anterior uveitis or non-chronic anterior uveitis.
9. The method of claim 1 , wherein the pharmaceutical composition comprises a polypeptide having at least 95% sequence identity to SEQ ID NO: 11.