AsiaIPEX is a one-stop-shop for players in the IP industry, facilitating IP trade and connection to the IP world. Whether you are a patent owner interested in selling your IP, or a manufacturer looking to buy technologies to upgrade your operation, you will find the portal a useful resource.

Matrix metalloproteinase inhibitors to treat tuberculosis

Summary
Tuberculosis is an airborne bacterial infection that capitalizes on enzymes produced by the body’s immune system to destroy lung tissue. In particular, the bacteria take advantage of the natural secretion of matrix metalloproteinases (MMPs), which degrade lung tissue and inadvertently facilitate bacterial proliferation. Current tuberculosis treatments consist primarily of antibiotic administration, but are often ineffective in the long term. This technology is an MMP inhibitor that aims to treat tuberculosis by preventing the degradation of lung tissue and subsequent growth of bacteria.
Technology Benefits
Reduces lung damage due to tuberculosisHinders proliferation of tuberculosis-causing bacteria in infected tissuePatent Information:Patent Pending (US 20140199289)Tech Ventures Reference: IR 2910
Technology Application
Tuberculosis therapyTherapy for patients with antibiotic-resistant tuberculosisTherapy for other diseases in which MMPs are implicated in tissue degradation
Detailed Technology Description
None
*Abstract
None
*Inquiry
Sara GusikColumbia Technology VenturesTel: (212) 854-8444Email: TechTransfer@columbia.edu
*IR
2910
*Principal Investigator
*Publications
Elkington P.T., D’Armiento J.M., Friedland J.S. “Tuberculosis Immunopathology: The Neglected Role of Extracellular Matrix Destruction.” Sci Translational Med. 2011 Feb 23;3(71):71ps6Elkington P.T., Shiomi T., Nuttall R.K, Ugarte-Gil C.A., Walker N.F., Saraiva L., Mauri F., Lipman M., Edwards D.R., Robertson B.D., D’Armiento J.M., Friedland J.S. “MMP-1 Drives Immunopathology in Human Tuberculosis and Transgenic Mice.” J Clin Invest. 2011 May 2;121(5):1827-1833
Country/Region
USA

For more information, please click Here
Mobile Device