US2013330740A1PendingUtilityA1
Novel therapeutic and diagnostic products and methods
Est. expiryJun 13, 2026(expired)· nominal 20-yr term from priority
A61P 43/00A61P 25/18A61P 25/24A61P 25/30A61P 25/00A61P 25/28A61P 25/22A61P 25/20A61P 15/00A61P 15/10A61P 1/00A61P 1/14A61P 1/04C12Q 2600/178G01N 2500/00C12N 2830/003A01K 2227/105G01N 33/942C07K 2319/41Y10T436/143333C12Q 2600/158C12Q 2600/136G01N 2800/30A01K 2217/20G01N 33/68G01N 33/6896G01N 2800/304C12Q 1/6883G01N 2500/04G01N 2333/46A01K 67/0276A61K 49/0008C12N 15/8509G01N 2500/10A01K 2217/052C12Q 1/6876A01K 2267/0356C12Q 2600/106C12Q 1/6886A01K 2217/075C07K 14/4721A01K 67/0275
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Claims
Abstract
The present invention relates to the use of p11 as a drug target as well as a tool for the diagnosis, treatment and development of p11/5-HT receptor related disorders. The invention further relates to p11 knock-out animals as well as p11 transgenic animals and their use as models for the development of novel psychotherapeutic agents, and to methods of diagnosis, prophylaxis and treatment of p11/5-HT receptor related disorders.
Claims
exact text as granted — not AI-modified1 - 39 . (canceled)
40 . A method of diagnosing a p11/5-HT receptor related disorders in a subject comprising determining the level of p11 in a biological sample wherein said sample comprises peripheral blood mononuclear cells from said subject and comparing said p11 level to a reference, wherein an abnormal level of p11 compared to the reference constitutes a positive diagnosis of p11/5-HT receptor related disorder.
41 . The method according to claim 40 , wherein said peripheral blood mononuclear cells are NK cells and/or CD-8+ T-cells.
42 . The method according to claim 40 , wherein said peripheral blood mononuclear cells are NK cells.
43 . The method according to claim 40 , wherein said p11/5-HT receptor related disorder is depression.
44 . The method according to claim 43 , wherein said depression comprises a p11 associated depression.
45 . The method according to claim 40 , wherein said p11/5-HT receptor related disorder is a disorder associated with an abnormally low level of p11, wherein reduced level of p11 in a subject compared to a control subject constitutes a positive diagnosis of such disorders.
46 . The method according to claim 45 , wherein said disorder associated with an abnormally low level of p11 is selected from a group consisting of depression, obsessive compulsive disorder, drug addiction, eating disorders, Alzheimer's disease, attention deficit disorder and attention deficit hyperactive disorder.
47 . The method according to claim 40 , wherein said p11/5-HT receptor related disorders are disorders associated with an abnormally high level of p11, wherein an elevated level of p11 in a subject compared to that in a control subject constitutes a positive diagnosis of such disorders.
48 . The method according to claim 47 , wherein said disorder associated with an abnormally high level of p11 is selected from a group consisting of mania, dipolar disorder, anxiety disorders, aggression, sleep disorders, sexual dysfunction and gastrointestinal disorders.
49 . The method according to claim 40 , wherein said level of p11 is determined by assaying p11 protein level in the monocytes and/or lymphocytes in said biological sample from said subject.
50 . The method according to claim 40 , wherein said level of p11 is determined by assaying p11 mRNA level in a biological sample from said subject.
51 . The method of claim 40 , wherein the level of p11 is determined using a monoclonal antibody specific for p11.
52 . The method of claim 50 , wherein the detection of said monoclonal antibody is achieved by using standard ELISA, FACS analysis, and/or standard imaging techniques.Join the waitlist — get patent alerts
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