IP Library Granted Patent US 9,995,756
Granted Patent B2
US 9,995,756 · App. 15/277,609 · Granted Jun 12, 2018

Buccal cell diagnosis of arrhythmogenic cardiomyopathy (ACM)

Inventors: Jeffrey E. Saffitz (Waban, MA); Angeliki Asimaki (Boston, MA)
Assignee: Beth Israel Deaconess Medical Center, Inc.
G01N33/6893G01N2800/325G01N2800/60
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Quick Facts
Patent No.
US 9,995,756
App. No.
15/277,609
Granted
Jun 12, 2018
Kind
B2
Abstract

Described herein are, inter alia, methods for diagnosing and treating arrhythmogenic cardiomyopathy (ACM) by detecting cardiac intercalated disk proteins, e.g., desmosomal proteins, mechanical and gap junction proteins, in buccal cells. Exemplary desmosomal and gap junction proteins that can be evaluated in the methods described herein include plakoglobin, plakophilin 1, desmoplakin, and Cx43. The methods can also include selecting and/or administering a treatment for ACM to the subject.

Claims (50)

1. A method comprising:

obtaining a sample comprising buccal cells from the subject; and

detecting one or both of the level or localization of one or more desmosomal or gap junction proteins selected from the group consisting of plakoglobin, plakophilin 1, desmoplakin, and Cx43 in the subject sample.

2. A method of diagnosing arrhythmogenic cardiomyopathy (ACM) in a subject, the method comprising:

obtaining a sample comprising buccal cells from the subject;

detecting the level or localization of one or more desmosomal or gap junction proteins selected from the group consisting of plakoglobin, plakophilin 1, desmoplakin, and Cx43 in the subject sample;

comparing the level or localization of the one or more cardiac intercalated disk or desmosomal proteins in the subject sample to a reference level or localization; and

diagnosing ACM in the subject when the level in the subject sample is below the reference level, or when the localization differs from the reference localization.

3. The method of claim 2 , where the reference level is a level in a subject who does not have ACM.

4. The method of claim 2 , wherein the reference localization is localization in a subject who does not have ACM, optionally localization to cellular junctions.

5. The method of claim 1 , wherein the buccal cells were obtained by rubbing the inside of the cheek of the subject with a swab, spatula, or scraper.

6. The method of claim 1 , comprising applying the buccal cells onto a surface; optionally fixing the cells; and contacting the cells with an antibody or antigen-binding fragment thereof that binds to a desmosomal or gap junction protein.

7. The method of claim 1 , comprising detecting the level and/or localization of plakoglobin;

plakophilin1;

desmoplakin;

Cx43;

plakoglobin and plakophilin1;

plakophilin1 and desmoplakin;

plakoglobin and desmoplakin;

plakophilin1 and Cx43;

plakoglobin and Cx43;

desmoplakin and Cx43;

plakoglobin, plakophilin 1, and Cx43;

plakoglobin, desmoplakin, and Cx43;

plakoglobin, plakophilin1, and desmoplakin;

plakophilin 1, desmoplakin, and Cx43; or

plakoglobin, plakophilin 1, desmoplakin, and Cx43.

8. The method of claim 1 , comprising detecting the level and/or localization of plakoglobin and Cx43.

9. The method of claim 1 , comprising contacting the subject sample with antibodies to:

plakoglobin;

plakophilin1;

desmoplakin;

Cx43;

plakoglobin and plakophilin1;

plakophilin1 and desmoplakin;

plakoglobin and desmoplakin;

plakophilin1 and Cx43;

plakoglobin and Cx43;

desmoplakin and Cx43;

plakoglobin, plakophilin 1, and Cx43;

plakoglobin, desmoplakin, and Cx43;

plakoglobin, plakophilin1, and desmoplakin;

plakophilin 1, desmoplakin, and Cx43; or

plakoglobin, plakophilin 1, desmoplakin, and Cx43.

10. The method of claim 1 , comprising contacting the subject sample with antibodies to plakoglobin and Cx43.

11. The method of claim 9 , wherein the antibodies are directly or indirectly labeled, and the method comprises detecting the labeled antibodies.

12. The method of claim 1 , wherein the subject is at least 7 years of age.

13. The method of claim 2 , further comprising selecting a subject diagnosed with ACM for treatment.

14. The method of claim 13 , further comprising administering the treatment for ACM to a subject diagnosed with ACM.

15. The method of claim 13 , wherein the treatment comprises one or more of recommending or advising the subject to avoid strenuous or intense physical activity or exercise; recommending or prescribing or administering one or more Singh Vaughan Williams class II antiarryhthmics (beta blockers) such as propranolol, esmolol, timolol, metoprolol, or atenolol; recommending or prescribing or administering one or more class III anti-arrhythmics (K-channel blockers) such as amiodarone, sotalol, ibutilide, dofetilide, dronedarone or E-4031; recommending or performing cardiac ablation; or recommending or implanting an implantable cardiac defibrillator (ICD).

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 2, 2016
From: SAFFITZ, JEFFREY E.; ASIMAKI, ANGELIKI
To: BETH ISRAEL DEACONESS MEDICAL CENTER, INC.
Reel/Frame 040497/0181 →
CONFIRMATORY LICENSE Recorded Nov 8, 2016
From: BETH ISRAEL DEACONESS MEDICAL CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 040576/0082 →
Continuity (2)
Provisional Application 62236006 · Oct 1, 2015
Related Publication 20170097363A1 · Apr 6, 2017