Claims for Patent: 10,378,055

Summary for Patent: 10,378,055

Title:	Methods and compositions for measuring beta cell death
Abstract:	Provided herein are, inter alia, nucleic acids, methods, and kits for detecting unmethylated DNA in body fluid sample of a subject. The disclosure includes compositions, methods, and kits for detecting unmethylation at a CpG site in an insulin gene promoter of a subject.
Inventor(s):	Ferreri; Kevin (Culver City, CA), Husseiny Elsayed; Mohamed I. (Torrance, CA)
Assignee:	City of Hope (Duarte, CA)
Application Number:	15/093,359
Patent Claims:	1. A method of detecting unmethylated deoxyribonucleic acid (DNA) in a subject, the method comprising isolating DNA from a blood sample of said subject; contacting said isolated DNA with bisulfite for modifying unmethylated cytosine at a CpG site in said DNA to uridine; and detecting unmethylation of said CpG site in an insulin gene promoter located at -19 bp, -69 bp, -135 bp, -206 bp, or -357 bp relative to the transcription start site. 2. The method of claim 1, wherein said detecting comprises: amplifying said DNA comprising uridine using quantitative methylation-specific polymerase chain reaction (qMSP) with methylation specific primers; thereby detecting unmethylation at said CpG site. 3. The method of claim 1 or 2, wherein said DNA is from beta cells of said subject. 4. The method of claim 3, wherein said beta cells are undergoing cell death. 5. The method of claim 4, wherein said beta cells are undergoing programmed cell-death. 6. The method of claim 4, wherein said beta cells are undergoing non-programmed cell death. 7. The method of claim 4, wherein said beta cells are undergoing death due to an autoimmune response. 8. The method of claim 2, wherein said methylation specific primer hybridizes to said CpG site. 9. The method of claim 8, wherein said methylation specific primer comprises SEQ ID NO: 1, 2, 3, or 4. 10. The method of claim 8, wherein said detecting unmethylation at said CpG site comprises detecting unmethylation at two or more of said CpG sites on said insulin gene promoter. 11. The method of claim 2, wherein said subject is a human with a family history of type I diabetes (T1D). 12. The method of claim 1, wherein said blood sample is whole blood, plasma, or serum of said subject. 13. A method of treating autoimmunity against beta cells in a subject having unmethylated CpG at -19 bp, -69 bp, -135 bp, -206 bp, or -357 bp relative to the transcription start site of an insulin gene promoter of beta cells, determined by the method as set forth in claim 2, comprising administering to said subject an agent for treating T1D, thereby treating T1D of said subject. 14. The method of claim 13, wherein the autoimmunity results in T1D. 15. The method of claim 13, wherein the agent is insulin. 16. The method of claim 15, wherein the insulin is administered by injection or an insulin pump. 17. The method of claim 13, wherein the agent is cyclosporine, anti-CD3 antibody, or anti-CD20 antibody. 18. The method of claim 13, wherein the agent is a cytokine selected from the group consisting of: human growth hormone, N-methionyl human growth hormone, and bovine growth hormone, parathyroid hormone, thyroxine, insulin, proinsulin, relaxin, prorelaxin, follicle stimulating hormone (FSH), thyroid stimulating hormone (TSH), luteinizing hormone (LH), hepatic growth factor, fibroblast growth factor, prolactin, placental lactogen, tumor necrosis factor .alpha. and/or .beta., mullerian-inhibiting substance, mouse gonadotropin-associated peptide, inhibin, activing, vascular endothelial growth factor, integrin, thrombopoietin (TPO), nerve growth factors such as NGF-.beta., platelet-growth factor, transforming growth factors (TGFs) TGF-.alpha. and/or TGF-.beta., insulin-like growth factor-I and/or -II, erythropoietin (EPO), osteoinductive factors; interferons such as interferon-.alpha., .beta., and .gamma.; colony stimulating factors (CSFs) such as macrophage-CSF (M-CSF), granulocyte-macrophage-CSF (GM-CSF), and granulocyte-CSF (G-CSF), interleukins (ILs) IL-1, IL-1.alpha., IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-11, IL-12, IL-13, IL-16, IL-17, IL-18, IL-22, IL-23, IL-27, IL-35, and/or IL-35; tumor necrosis factor TNF-.alpha. and/or TNF-.beta.; and kit ligand (KL). 19. The method of claim 13, wherein the agent is for immunotherapy to ameliorate autoimmunity against beta cells, and symptoms thereof. 20. The method of claim 13, further comprising transplanting pancreas or islet cells to said subject. 21. A system, comprising: at least one processor; and at least one memory including program code which when executed by the one memory provides operations comprising: collecting deoxyribonucleic acid (DNA) data associated with a subject; contacting isolated DNA from a blood sample of a subject with bisulfite for modifying unmethylated cyctosine at a CpG site in said DNA to uridine detecting unmethylation of DNA at said CpG site in an insulin gene promoter located at -19 bp, -69 bp, -135 bp, -206 bp, or -357 bp relative to the transcription start site; and providing, via a user interface, a prognosis and/or diagnosis for the subject based at least in part on detected unmethylated DNA. 22. The system of claim 21, further configured to provide, via the user interface, a treatment plan determined based at least in part on the prognosis and/or diagnosis. 23. The system of claim 21, wherein the detecting of unmethylation at the CpG site comprises detecting unmethylation at two or more CpG sites on the insulin gene promoter. 24. The system of claim 21, wherein the subject comprises a human having a family history of a type of diabetes. 25. The system of claim 21, wherein the blood sample comprises whole blood, plasma, or serum. 26. The system of claim 21, wherein the DNA data comprises sequencing data corresponding to DNA isolated from a blood sample of the subject. 27. The system of claim 26, wherein the isolated DNA is modified by at least modifying unmethylated cystosine in the isolated DNA to produce DNA that includes uridine. 28. The system of claim 27, wherein the DNA that includes uridine is amplified by quantitative methylation-specific polymerase chain reaction (qMSP) with methylation specific primers. 29. The system of claim 28, wherein the methylation specific primer hybridizes to the CpG site. 30. The system of claim 28, wherein the methylation specific primer comprises SEQ ID NO: 1, 2, 3, or 4. 31. The system of claim 26, wherein the DNA comprises DNA from beta cells of the subject. 32. The system of claim 31, wherein the beta cells comprise cells undergoing programmed or non-programmed cell-death as a result of an autoimmune response.

Details for Patent 10,378,055

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Nps Pharmaceuticals, Inc.	NATPARA	parathyroid hormone	For Injection	125511	01/23/2015		2035-04-08