The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Oct. 31, 2017

Filed:

Feb. 16, 2016
Applicants:

Moleculera Labs, Inc., Oklahoma City, OK (US);

The Board of Regents of the University of Oklahoma, Norman, OK (US);

National Institutes of Health, Bethesda, MD (US);

Inventors:

Phina Madeleine Cunningham, Oklahoma City, OK (US);

Craig David Shimasaki, Edmond, OK (US);

Susan E. Swedo, McLean, VA (US);

Christine Kirvan, Lincoln, CA (US);

Assignees:

The Board of Regents of the University of Oklahoma, Norman, OK (US);

Moleculera Labs, Inc., Oklahoma City, OK (US);

National Institutes of Health, Bethsesda, MD (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 38/00 (2006.01); G01N 33/53 (2006.01); G01N 33/68 (2006.01); G01N 33/564 (2006.01); G01N 33/569 (2006.01);
U.S. Cl.
CPC ...
G01N 33/686 (2013.01); G01N 33/564 (2013.01); G01N 33/56944 (2013.01); G01N 33/6854 (2013.01); G01N 33/6896 (2013.01); G01N 2333/315 (2013.01); G01N 2333/726 (2013.01); G01N 2333/912 (2013.01); G01N 2405/10 (2013.01); G01N 2469/20 (2013.01); G01N 2800/26 (2013.01); G01N 2800/28 (2013.01); G01N 2800/30 (2013.01); G01N 2800/38 (2013.01);
Abstract

The present invention provides a panel of at least five clinical analyses or tests (using serum samples) to determine the risk of pediatric acute-onset neuropsychiatric syndrome (PANS) and/or pediatric autoimmune neuropsychiatric disorder associated with streptococcal infection (PANDAS) in an individual. These include enzyme linked immunosorbent assays (ELISAs) to measure antibody titers against neuronal antigens present in the brain; the neuronal antigens include lysoganglioside, tubulin, dopamine receptor D1, dopamine receptor D2, serotonin receptor 5HT2A, and serotonin receptor 5HT2C. Antibody titers against at least four of these neuronal antigens are required in the present methods; preferably antibody tiers against all of these neuronal antigens are measured. A final assay is used to quantify calcium/calmodulin-dependent protein kinase activity using a neuronal cell line. The results of these analyses or tests are then combined using an algorithm to determine whether a PANS or PANDAS diagnosis is appropriate for the individual. Depending on the diagnosis, an appropriate treatment can be determined.


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