http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2875535-T3

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filingDate 2013-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1f9538c69107d618678f4a12eadbefc
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publicationDate 2021-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2875535-T3
titleOfInvention Biomarkers for use in Integrin Therapy Applications
abstract A method of predicting whether a human subject having an αvβ6-mediated disorder will respond to treatment with an αvβ6 integrin inhibitor, the method comprising: a) providing a biological sample that has been obtained from the human subject after administration of the integrin inhibitor αvβ6; and b) measuring the expression level of one or more genes or proteins selected from the group consisting of arachidonate 5-lipoxygenase 5 (ALOX5), fibronectin (FN1), oxidized low-density lipoprotein receptor 1 (OLR1), inhibitor of activator of plasminogen 1 (PAI-1 or SERPINE1), transglutaminase 2 (TGM2), and trigger receptor expressed in myeloid cells 1 (TREM1) in the biological sample, in which a decrease in the expression level of one or more genes or proteins relative to a control expression level predicts that the human subject will respond, or is more likely to respond, to treatment with the αvβ6 integrin inhibitor, wherein the αvβ6-mediated disorder is selected from the group consisting of pulmonary fibrosis, pulmonary fibrosis idiopathic, radiation-induced fibrosis, bleomycin-induced fibrosis, asbestos-induced fibrosis, lung cancer and acute lung injury, scleroderma, in which αvβ6 integrin inhibitor is an an αvβ6 anti-integrin antibody, and wherein the biological sample is bronchoalveolar lavage fluid.
priorityDate 2012-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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