发明名称 Diagnostic method for brain damage-related disorders
摘要 A brain damage-related disorder is diagnosed in a subject by detecting at least one polypeptide, or a variant or mutant thereof, in a sample of body fluid taken from the subject, wherein the polypeptide is one for which the level is either increased or decreased in cerebrospinal fluid from deceased patients compared to cerebrospinal fluid from healthy donors.
申请公布号 US9028825(B2) 申请公布日期 2015.05.12
申请号 US200611995501 申请日期 2006.07.14
申请人 Universite de Geneve 发明人 Hochstrasser Denis Francois;Sanchez Jean-Charles
分类号 A61K39/395;C07K16/40;G01N33/68 主分类号 A61K39/395
代理机构 Arent Fox LLP 代理人 Arent Fox LLP
主权项 1. A method of diagnosis of a brain damage-related disorder selected from stroke and sub-arachnoid hemorrhage in a subject comprising: (a) detecting a level of expression of glutathione S transferase P and at least one polypeptide selected from the group consisting of peroxiredoxin 1, peroxiredoxin 2, peroxiredoxin 5, and peroxiredoxin 6, or variants or mutants thereof in a sample of plasma, serum or cerebrospinal fluid taken from the subject, wherein the variants or mutants have a homology of at least 90% with the polypeptide; (b) detecting a level of expression of the glutathione S transferase P and the polypeptide in a control sample of plasma, serum or cerebrospinal fluid taken from a control subject known not to have suffered from the brain damage-related disorder; and (c) diagnosing the subject as having suffered from the brain damage-related disorder when the level-of expression of glutathione S transferase P and the at least one polypeptide in the sample is higher than the level of expression in the control sample, and wherein detecting the level of expression in the sample (a) and the control sample (b) comprises: immunodepletion of abundant proteins in the sample or the control sample; and assaying the immunodepleted sample or control sample using an antihuman GST-P antibody and an antibody that recognizes, binds to or has affinity for a polypeptide selected from the group consisting of peroxiredoxin 1, peroxiredoxin 2, peroxiredoxin 5 and peroxiredoxin 6 and mutants or variants thereof in the sample or the control sample, wherein the variants or mutants have a homology of at least 90% with the polypeptide.
地址 Geneva CH