US2014315205A1PendingUtilityA1
Treatment and diagnosis of immune disorders
Est. expiryJul 15, 2029(~3 yrs left)· nominal 20-yr term from priority
A61P 37/00A61P 29/00A61P 31/00A61P 11/00C12Q 2600/158C12Q 1/68C12N 2310/14C12Q 2600/106C12N 15/113C12Q 1/6883C12Q 2600/178A61K 31/7105
59
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Disclosed are composition and methods for treating immune disorders. Also disclosed are diagnosis methods and prognosis methods.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for managing patient treatment comprising
identifying a patient under, or in need of, a treatment for a condition, obtaining a biological sample from the patient, and determining the expression level of a gene encoding a polypeptide containing SEQ ID NO: 1 in the sample,
wherein the patient is determined to be suitable for the treatment if the level is at or above a predetermined value.
2 . The method of claim 1 , wherein the method further comprises communicating the expression level to the patient or to a physician or a caretaker of the patient.
3 . The method of claim 1 , wherein the condition is a cellular proliferative disorder.
4 . The method of claim 1 , wherein the condition is an inflammatory or autoimmune disorder.
5 . A kit for diagnosing an immune disorder or for managing patient treatment, comprising one or more reagents selected from the group consisting of
an antibody specific for a polypeptide having the sequence of SEQ ID NO: 1, a polypeptide having the sequence of SEQ ID NO: 1, a pair of PCR primers for amplifying a fragment of SEQ ID NO:2 or 3, and a nucleic acid that, under a stringent condition, hybridizes to the compliment of a reference nucleic acid, wherein the reference nucleic acid consists of SEQ ID NO:2 or 3.
6 . The method of claim 5 , wherein the disorder is ALL, CLL, AML, MDS, SLE, IBD, RA, or transplant rejection.
7 . A method of diagnosing an immune disorder in a subject, the method comprising obtaining a biological sample from the subject; and determining the expression level of a gene encoding a polypeptide containing SEQ ID NO:1 in the sample.
8 . The method of claim 7 , wherein the disorder is a cellular proliferative disorder and the subject is determined to have or be prone to develop the cellular proliferative disorder if the expression level is below a first predetermined level or absent.
9 . The method of claim 7 , wherein the disorder is an inflammatory or autoimmune disorder and the subject is determined to have or be prone to develop the disorder if the expression level is above a second predetermined level.
10 . The method of claim 7 , wherein the determining step is carried out with a pair of PCR primers for amplifying a fragment of SEQ ID NO:2 or 3.
11 . The method of claim 7 , wherein the determining step is carried out with an oligonucleotide that, under a stringent condition, hybridizes to the compliment of a reference nucleic acid, wherein the reference nucleic acid is the sequence of SEQ ID NO:2 or 3.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.