IP Library Granted Patent US 7,794,958
Granted Patent B2
US 7,794,958 · App. 12/018,010 · Granted Sep 14, 2010

Methods for diagnosing endometriosis

Assignee: The Board of Trustees of the University of Illinois
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Quick Facts
Patent No.
US 7,794,958
App. No.
12/018,010
Granted
Sep 14, 2010
Kind
B2
Abstract

Provided herein is a method for diagnosing and monitoring endometriosis in a subject by measuring levels of the β-subunit of fibrinogen.

Claims (18)

1. A method for diagnosing endometriosis in a subject, comprising:

(a) providing a sample isolated from the subject; and

(b) measuring the level of fibrinogen β-subunit in the sample;

wherein a level of fibrinogen β-subunit lower than the level of a control is indicative of endometriosis.

2. The method of claim 1 , wherein the level of fibrinogen β-subunit is between 0 and 95% of the level of the control.

3. The method of claim 2 , wherein the level of fibrinogen β-subunit is between 0 and 70% lower than the control.

4. The method of claim 1 , wherein measuring the level of fibrinogen β-subunit comprises contacting fibrinogen β-subunit with a fibrinogen β-subunit binding partner.

5. The method of claim 4 , wherein the binding partner is an antibody.

6. The method of claim 5 , wherein the antibody is monoclonal.

7. The method of claim 6 , wherein the antibody is selected from the group consisting of: rabbit polyclonal fibrinogen anti-human antibody (Dako Cat. No. A0080), F4639 monoclonal anti-fibrinogen antibody produced in mouse (Sigma-Aldrich clone FG-21, ascites fluid), F9902 monoclonal anti-fibrinogen antibody produce in mouse (Sigma-Aldrich clone 85D4, ascites fluid), and anti-fibrinogen antibody produced in goat (Sigma-Aldrich clone F8512, whole antiserum).

8. The method of claim 4 , wherein the binding partner further comprises a label.

9. The method of claim 1 , wherein the level of fibrinogen β-subunit is measured using a detection method selected from the group consisting of: Western blot, two-dimensional gel electrophoresis, mass spectrometry (MS), tandem mass spectrometry, and multiple rounds of mass spectrometry.

10. The method of claim 9 , wherein the mass spectrometry comprises using a mass analyzer.

11. The method of claim 10 , wherein the mass analyzer is selected from the group consisting of: ion trap, triple quadrupole, time-of-flight, quadrupole-time-of-flight mass spectrometry, and Fourier transform ion cyclotron mass spectrometry (FT-ICR-MS).

12. The method of claim 10 , wherein the mass spectrometry further comprises a matrix-assisted laser desorption (MALDI) or electrospray ionization (ESI) ion source.

13. The method of claim 1 , wherein the subject is a mammal.

14. The method of claim 13 , wherein the mammal is a human.

15. The method of claim 1 , wherein the sample is selected from the group consisting of: blood, lymph fluid, ascetic fluid, gynecological fluid, urine, peritoneal fluid, cerebrospinal fluid, a fluid collected by vaginal rinsing, and a fluid collected by vaginal flushing.

Assignments (3)
CONFIRMATORY LICENSE Recorded Aug 15, 2010
From: UNIVERSITY OF ILLINOIS AT CHICAGO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024837/0634 →
CONFIRMATORY LICENSE Recorded Sep 23, 2009
From: UNIVERSITY OF ILLINOIS AT CHICAGO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 023270/0151 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2008
From: FAZLEABAS, ASGERALLY T.
To: THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS
Reel/Frame 020625/0392 →
Continuity (2)
Provisional Application 6088130000 · Jan 19, 2007
Related Publication 20080299676A1 · Dec 4, 2008