Anti-emp2 therapy reduces cancer stem cells
US-2015329621-A1 · Nov 19, 2015 · US
US10385395B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10385395-B2 |
| Application number | US-201314391814-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 11, 2013 |
| Priority date | Apr 11, 2012 |
| Publication date | Aug 20, 2019 |
| Grant date | Aug 20, 2019 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
NK cell licensing predisposes patients to chronic inflammatory disease. Methods and kits to diagnose and treat chronic inflammatory disease based on genetic haplotype and cytokine profile are described herein.
Opening claim text (preview).
We claim: 1. A method for treating a patient having a chronic inflammatory disease, the method comprising administering a 6-thiopurine or 6-thioguanine treatment regimen to the patient having the chronic inflammatory disease, wherein the patient is determined have a KIR/HLA-haplotype of an AA haplotype, homozygous for HLA-C1 and present for Bw6; a non-AA haplotype, present for KIR2DL2 and homozygous for HLA-C1; a non-AA haplotype, present for KIR2DL2 and heterozygous for HLA-C1/HLA-C2; or a non-AA haplotype, absent for KIR2DL2 and homozygous for HLA-C1, based on a KIR/HLA haplotype determination of the patient, and wherein the KIR/HLA-haplotype of the patient is determined by: (a) providing a biological sample from the patient; (b) obtaining nucleic acid from the biological sample; and (c) hybridizing the nucleic acid, to: (i) a first solid support comprising synthetic capture probes selective for KIR2DL3, KIR2DL1, KIR2DL4, KIR3DL1, KIR3DL2, KIR3DL3, KIR2DS4, KIR2DP1, KIR3DP1, KIR2DL5, KIR2DS1, KIR2DS2, KIR2DS3, KIR2DS5, and KIR3DS1; and (ii) a second solid support comprising capture probes selective for HLA-C1, HLA-C2, HLA-Bw4 and HLA-Bw6. 2. The method of claim 1 , wherein the biological sample is a blood sample. 3. The method of claim 1 , wherein the patient is a human. 4. The method of claim 1 , wherein the treatment regimen is a 6-thioguanine treatment regimen.
Antineoplastic agents · CPC title
Pharmacogenomics, i.e. genetic variability in individual responses to drugs and drug metabolism · CPC title
related to diseases not provided for elsewhere · CPC title
Bowel diseases, e.g. Crohn, ulcerative colitis, IBS · CPC title
Haplotypes · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.