IP Library Granted Patent US 10,793,909
Granted Patent B2
US 10,793,909 · App. 15/775,092 · Granted Oct 6, 2020

Methods for predicting the survival time of patients with decompensated alcoholic cirrhosis

Inventors: Richard Moreau (Paris, FR); Emmanuel Weiss (Paris, FR); Pierre-Emmanuel Rautou (Paris, FR)
Assignees: INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE); UNIVERSITE PARIS DESCARTES; ASSISTANCE PUBLIQUE—HOPITAUX DE PARIS (APHP); UNIVERSITE PARIS DIDEROT—PARIS 7
C12Q1/6883C12Q2600/118C12Q2600/158
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,793,909
App. No.
15/775,092
Granted
Oct 6, 2020
Kind
B2
Abstract

The present invention relates to methods for predicting the survival time of patients with decompensated alcoholic cirrhosis. In particular, the present invention relates to a method for predicting the survival time of a patient with decompensated alcoholic cirrhosis comprising i) determining the expression level of OAS2 or MX2 in a sample of peripheral blood mononuclear cells obtained from the patient, ii) comparing the level determined at step i) with a predetermined reference value and iii) and concluding that the patient will have a short survival time when the level determined at step i) is higher than its predetermined reference value or concluding that the patient will have a long survival time when the level determined at step i) is lower than the predetermined reference value.

Claims (11)

1. A method of treating a patient with decompensated alcoholic cirrhosis having a decreased survival time comprising

i) determining the mRNA expression level of OAS2 or MX2 in a sample of peripheral blood mononuclear cells obtained from the patient,

ii) comparing the level determined at step i) with the mRNA expression level of OAS2 or MX2 in healthy subjects,

iii) determining that the patient will have a decreased survival time when the level determined at step i) is higher than the mRNA expression level of OAS2 or MX2 in healthy subjects, and

iv) performing liver transplantation on the patient determined to have a decreased survival time.

2. The method of claim 1 wherein the expression levels of OAS2 and MX2 are determined at step i).

3. The method of claim 1 wherein the expression level of at least one further gene is determined and compared to its corresponding expression level in healthy subjects.

4. The method of claim 3 wherein the gene for which the expression is further determined is selected from the group consisting of IFIT1, CXCL10, IFIH1, DDX58, TRIM22 and GBP4.

5. The method of claim 4 wherein the expression levels of 2, 3, 4, 5, 6, 7 or 8 genes are determined.

6. The method of claim 4 wherein the expression levels of OAS2, MX2, IFIT1, CXCL10, IFIH1, DDX58, TRIM22 and GBP4 are determined in the sample.

7. The method of claim 1 wherein the expression level of the gene is determined by RT-PCR.

Assignments (3)
MERGER AND CHANGE OF NAME Recorded May 3, 2022
From: UNIVERSITE PARIS DESCARTES; UNIVERSITÉ PARIS DIDEROT - PARIS 7; UNIVERSITE DE PARIS
To: UNIVERSITE DE PARIS
Reel/Frame 059795/0703 →
CHANGE OF NAME Recorded May 3, 2022
From: UNIVERSITE DE PARIS
To: UNIVERSITÉ PARIS CITÉ
Reel/Frame 059925/0756 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2020
From: MOREAU, RICHARD; WEISS, EMMANUEL; RAUTOU, PIERRE-EMMANUEL
To: INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE); UNIVERSITE PARIS DESCARTES; ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (APHP); UNIVERSITE PARIS DIDEROT - PARIS 7
Reel/Frame 052879/0482 →
Priority Claims (1)
EP 15306785 · Nov 10, 2015 · regional
Continuity (1)
Related Publication 20180320232A1 · Nov 8, 2018