IP Library Granted Patent US 9,394,517
Granted Patent B2
US 9,394,517 · App. 14/135,630 · Granted Jul 19, 2016

CD4+ T-cells with cytolytic properties

Inventor: Jean-Marie Saint-Remy (Grez-Doiceau, BE)
Assignee: IMCYSE SA
C12N5/0636A61K2035/124A61K2039/57A61K2039/627C12N2501/23
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Quick Facts
Patent No.
US 9,394,517
App. No.
14/135,630
Granted
Jul 19, 2016
Kind
B2
Abstract

The present invention relates to CD4+ T cells, more specifically cytolytic or cytotoxic CD4+ T-cells and methods of obtaining and identifying them.

Claims (17)

1. A method of identifying a population of cytolytic CD4+ T-cells, said method comprising the steps of:

(i) providing isolated natural CD4+ regulatory T-cells;

(ii) providing isolated CD4+ T cells suspected of being cytolytic; wherein the CD4+ T cells suspected of being cytolytic are obtained by a method comprising contacting natural naive or memory CD4+ T cells with an immunogenic peptide comprising an MHC class II T cell epitope and adjacent to said T cell epitope or separated therefrom by at most 7 amino acids a C-(X)2-[CST] or [CST]-(X)2-C motif,

or wherein the CD4+ T cells suspected of being cytolytic are obtained by a method comprising administering an immunogenic peptide comprising an MHC class II T cell epitope and adjacent to said T cell epitope or separated therefrom by at most 7 amino acids a C-(X)2-[CST] or [CST]-(X)2-C motif to a subject, and collecting of CD4+ T cells generated in vivo from said subject; and

(iii) measuring that the CD4+ T-cells suspected of being cytolytic provided in (ii) display, compared to the isolated natural CD4+ regulatory T-cells provided in (i), undetectable expression of the transcription repressor Foxp3, and increased activity of serine-threonine kinase AKT.

2. The method according to claim 1 , said method further comprising determining in step (iii) that the T-cells provided in (ii) display, compared to the T-cells provided in (i), undetectable production of TGF-beta and undetectable or very low production of IL-10.

3. The method according to claim 1 , said method further comprising determining in step (iii) that the T-cells provided in (ii) display, compared to the T-cells provided in (i), production of high concentrations of IFN-gamma.

4. The method according to claim 1 , said method further comprising determining in step (iii) that the T-cells provided in (ii) display, compared to the T-cells provided in (i), production of high concentrations of soluble Fas ligand (FasL).

5. A method of identifying a population of cytolytic CD4+ T-cells, said method comprising the steps of:

(i) providing isolated natural CD4+ regulatory T-cells;

(ii) providing isolated natural naïve or memory CD4+ T-cells;

(iii) contacting said isolated natural naïve or memory CD4+ T-cells with an immunogenic peptide comprising a T-cell epitope and, adjacent to said T-cell epitope or separated therefrom by a linker of at most 7 amino acids, a C-(X)2-[CST] or [CST]-(X)2-C motif; and

(iv) measuring that the cells obtained in step (iii) display, compared to the isolated natural CD4+ regulatory T-cells provided in (i), undetectable expression of the transcription repressor Foxp3, and an increased activity of serine-threonine kinase AKT.

6. A method of identifying a population of cytolytic CD4+ T-cells, said method comprising the steps of:

(i) providing isolated natural CD4+ regulatory T-cells;

(ii) providing isolated CD4+ T-cells suspected of being cytolytic, wherein the CD4+ T cells suspected of being cytolytic are obtained by a method comprising administering an immunogenic peptide comprising an MHC class II T cell epitope and adjacent to said T cell epitope or separated therefrom by at most 7 amino acids a C-(X)2-[CST] or [CST]-(X)2-C motif to a subject, and collecting of CD4+ T cells generated in vivo from said subject; and

(iii) measuring that the CD4+ T-cells suspected of being cytolytic provided in (ii) display, compared to the isolated natural CD4+ regulatory T-cells provided in (i), undetectable expression of the transcription repressor Foxp3, and increased activity of serine-threonine kinase AKT.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 8, 2021
From: LIFE SCIENCES RESEARCH PARTNERS; KATHOLIEKE UNIVERSITEIT LEUVEN
To: IMCYSE SA
Reel/Frame 058330/0536 →
LICENSE Recorded Aug 11, 2015
From: KATHOLIEKE UNIVERSITEIT LEUVEN; LIFE SCIENCES RESEARCH PARTNERS VZW
To: IMCYSE SA
Reel/Frame 036297/0237 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 28, 2015
From: LIFE SCIENCES RESEARCH PARTNERS VZW
To: LIFE SCIENCES RESEARCH PARTNERS VZW; KATHOLIEKE UNIVERSITEIT LEUVEN
Reel/Frame 034830/0775 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 14, 2014
From: SAINT-REMY, JEAN-MARIE
To: LIFE SCIENCES RESEARCH PARTNERS VZW
Reel/Frame 032437/0730 →
Priority Claims (1)
EP 08447006 · Feb 14, 2008 · regional
Continuity (3)
Continuation 12735741
Provisional Application 61035908
Related Publication 20140186297A1 · Jul 3, 2014