Methods for treating adult respiratory distress syndrome
We have discovered that the activated phosphorylated form of focal adhesion kinase (hereafter “FAKp”) strengthens the microvascular endothelial cell (EC) junctions that form a barrier in pulmonary endothelia, and the increased barrier helps to prevent acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). Thus certain embodiments of the invention are directed to prevention and treatment of ALI and ARDS by administering a therapeutically effective amount of FAKp to subjects at risk of developing or diagnosed as having either ALI or ARDS.
1. A method for treating or preventing acute lung injury and acute respiratory distress syndrome in an animal, comprising administering a therapeutically effective amount of activated phosphorylated focal adhesion kinase wherein the tyrosine at position 397 is phosphorylated or a biologically active fragment, derivative or variant thereof.
2. The method of claim 1 , wherein the activated focal adhesion kinase is human activated phosphorylated focal adhesion kinase.
3. The method of claim 2 , wherein the human activated phosphorylated focal adhesion kinase is a recombinant protein.
4. The method of claim 1 , further comprising administering a therapeutically effective amount of high osmolar sucrose.
5. The method of claim 4 , wherein the activated phosphorylated focal adhesion kinase and high osmolar sucrose are administered on the same day.
6. The method of claim 1 , wherein the activated phosphorylated focal adhesion kinase is administered intravenously or by inhalation.
7. The method as in claim 1 , wherein the therapeutically effective amount of activated phosphorylated focal adhesion kinase is an amount of from about 0.1-20 micrograms/kilogram body weight.
8. The method of claim 1 , wherein the activated focal adhesion kinase is bound to a transport protein that is a member selected from the group comprising Chariot™, pepetratin, TAT fragment, a signal sequence-based peptide, and transportan.