IP Library › Granted Patent US 11,406,280
Granted Patent B2
US 11,406,280 · App. 15/761,520 · Granted Aug 9, 2022

Method for the diagnosis of airway disease inflammatory subtype

Inventors: Florence Schleich (Liege, BE); Renaud Louis (Liege, BE); Kyrylo Bessonov (Liege, BE); Kristel Van Steen (Liege, BE); Frederik-Jan Van Schooten (Maastricht, NL); Jan Dallinga (Maastricht, NL)
Assignees: UNIVERSITE DE LIEGE; CENTRE HOSPITALIER UNIVERSITAIRE DE LIEGE
A61B5/082A61B5/097G01N30/7206G01N33/497
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Quick Facts
Patent No.
US 11,406,280
App. No.
15/761,520
Granted
Aug 9, 2022
Kind
B2
Abstract

In vitro methods for diagnosing, prognosing and/or monitoring and treating neutrophilic or eosinophilic airway inflammation in a subject, including determining the amount of one or more volatile organic compounds (VOCs) in exhaled breath from said subject. The invention also provides devices for use in said methods.

Claims (26)

1. A method of treatment of neutrophilic airway inflammation in a subject, wherein the airway inflammation is asthma, comprising the steps of:

a) determining whether the subject is in need of receiving neutrophilic asthma treatment by performing an in vitro procedure of diagnosing, prognosing and/or monitoring neutrophilic asthma in the subject, comprising the sub-steps of:

a1) determining an amount of one or more volatile organic compounds (VOCs) in a sample of exhaled breath from the subject;

a2) comparing the amount of the one or more VOCs with a reference value, the reference value representing a known diagnosis, prognosis and/or monitoring status of neutrophilic asthma;

a3) finding a deviation or no deviation of the amount of said one or more VOCs from the reference value; and

a4) attributing said finding of deviation or no deviation to a particular diagnosis, prognosis and/or monitoring status of neutrophilic asthma in the subject;

b) treating the subject diagnosed, prognosed and/or monitored in step a) as being in need of neutrophilic asthma treatment with a treatment selected from the group consisting of macrolides, anti-leukotriene agents, bronchodilators, and combinations thereof;

wherein the one or more volatile organic compounds (VOCs) is/are selected from the group consisting of:

3-tetradecene, and

1-pentadecene; and the method discriminates neutrophilic asthma from paucigranulocytic asthma in the subject; and

wherein:

the reference value is the amount of the same one or more VOCs in a sample of exhaled breath from the subject suffering from paucigranulocytic asthma; and wherein

an elevated amount of said one or more VOCs from said reference value is diagnostic or prognostic of neutrophilic asthma and/or of absence of paucigranulocytic asthma in the subject.

2. A method of treatment of neutrophilic airway inflammation in a subject, wherein the airway inflammation is asthma, comprising the steps of:

a) determining whether the subject is in need of receiving neutrophilic asthma treatment by performing an in vitro procedure of diagnosing, prognosing and/or monitoring neutrophilic asthma in the subject, comprising the sub-steps of:

a1) determining an amount of one or more volatile organic compounds (VOCs) in a sample of exhaled breath from the subject;

a2) comparing the amount of the one or more VOCs with a reference value, the reference value representing a known diagnosis, prognosis and/or monitoring status of neutrophilic asthma;

a3) finding a deviation or no deviation of the amount of said one or more VOCs from the reference value; and

a4) attributing said finding of deviation or no deviation to a particular diagnosis, prognosis and/or monitoring status of neutrophilic asthma in the subject;

b) treating the subject diagnosed, prognosed and/or monitored in step a) as being in need of neutrophilic asthma treatment with a treatment selected from the group consisting of macrolides, anti-leukotriene agents, bronchodilators, and combinations thereof;

wherein the one or more volatile organic compounds (VOCs) is/are selected from the group consisting of:

3-tetradecene, and

1-pentadecene; and the method discriminates neutrophilic asthma from paucigranulocytic asthma in the subject; and

wherein:

the reference value is the amount of the same one or more VOCs in a sample of exhaled breath from the subject suffering from neutrophilic asthma; and wherein

no deviation of the amount of said one or more VOCs from said reference value is diagnostic or prognostic of neutrophilic asthma and/or of absence of paucigranulocytic asthma in the subject.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2018
From: SCHLEICH, FLORENCE; LOUIS, RENAUD; BESSONOV, KYRYLO; VAN STEEN, KRISTEL; VAN SCHOOTEN, FREDERIK-JAN; DALLINGA, JAN
To: UNIVERSITE DE LIEGE
Reel/Frame 045713/0859 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2018
From: SCHLEICH, FLORENCE; LOUIS, RENAUD; BESSONOV, KYRYLO; VAN STEEN, KRISTEL; VAN SCHOOTEN, FREDERIK-JAN; DALLINGA, JAN
To: CENTRE HOSPITALIER UNIVERSITAIRE DE LIEGE
Reel/Frame 045713/0935 →
Priority Claims (1)
EP 15185986 · Sep 21, 2015 · regional
Continuity (1)
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