Method for the identification and separation of non-regulatory T-cells from a mixture of regulatory T-cells
View Patent ↗The present invention relates to a method of identifying and separating non-regulatory T-cells (conventional T-cells) from a mixture comprising regulatory T-cells by using of the CD154 molecule (CD40 ligand) through depletion of CD154+ T-cells from the mixture or in combination with additional positive selection of Treg using markers that are specific for regulatory T-cells, such as for example, CD25, GITR, CTLA4 or markers which are specific for activated regulatory T-cells, such as, for example, CD137, “latent TGF-beta (LAP)”, GARP (LRRC32), CD121a/b, thereby generating a cell composition of activated Treg cells. The invention relates also to a kit comprising an antibody for detecting CD154 and at least one additional antibody for detecting markers for activated or non-activated regulatory T-cells. The antibodies can be coupled to a fluorescent dye or magnetic microparticles.
1. A method of producing a pharmaceutical composition comprising an enriched cell population of activated regulatory T-cells not expressing CD154, the method comprising:
(A) preparing said enriched cell population by a process that comprises:
(1) obtaining a cell mixture comprising activated T-cells, the mixture containing both activated regulatory T-cells and other T-cells;
(2) contacting the cell mixture with a molecule that specifically binds CD154;
(3) separating and recovering cells from the mixture that have not bound to the molecule in step (2); and
(4) further enriching the cells for expression of at least one additional marker that is different from CD154 and is specifically present on regulatory T-cells or activated regulatory T-cells by contacting the cell mixture with a molecule that specifically binds the additional marker and recovering cells that have bound thereto, wherein step (4) is conducted before the contacting of step (2) or during or after the separating step of step (3); and
(B) formulating the enriched cell population prepared according to step (A) as a pharmaceutical composition suitable for administration to a human subject;
thereby producing a pharmaceutical composition comprising an enriched population of activated regulatory T-cells not expressing CD154.
2. The method of claim 1 , wherein the process for preparing the enriched cell population comprises:
(a) contacting the cell mixture comprising activated T-cells with a first molecule that specifically binds CLD154;
(b) depleting CD154 positive T-cells from the mixture by recovering cells that have not bound to the first molecule following step (a);
(c) contacting the cells from step (b) with a second molecule that specifically binds an additional marker that is different from CD154 and is specifically expressed on regulatory T-cells or activated regulatory T-cells;
(d) positively selecting cells that bind to the second molecule in step (c); and
(e) recovering cells that have bound the second molecule but not the first, thereby producing the enriched cell population.
3. The method of claim 1 , wherein the process for preparing the enriched cell population comprises:
(a) contacting the cell mixture comprising activated T-cells with a first molecule that specifically binds an additional marker that is different from CD154 and is specifically expressed on regulatory T-cells or activated regulatory T-cells;
(b) positively selecting cells that bind to the first molecule in step (a);
(c) contacting cells selected in step (b) with a second molecule that specifically binds CD154;
(d) depleting CD154 positive T-cells that have bound the second molecule in step (c); and
(e) recovering cells that have bound the first molecule but not the second, thereby producing the enriched cell population.
4. The method of claim 1 , claim 2 or claim 3 , wherein the additional marker is selected from CD25 and GITR.
5. The method of claim 1 , claim 2 or claim 3 , wherein the additional marker is selected from CD137, latent TGF-beta (LAP), GARP (LRRC32) and CD121a/b.
6. The method of claim 1 , wherein the molecule binding CD154 is an antibody or antibody fragment.
7. The method of claim 2 or claim 3 , wherein the molecule binding the additional marker is an antibody or antibody fragment.
8. The method of claim 1 , wherein the cell mixture has been obtained by stimulating T-cells in vivo.
9. The method of claim 1 , wherein the cell mixture has been obtained by stimulating T-cells in vitro.
10. The method of claim 8 or claim 9 , wherein the T-cells have been stimulated through their specific antigens or by polyclonal stimuli.
11. The method of claim 8 or claim 9 , wherein the activated regulatory T-cells are separated during stimulation of cells in the cell mixture.
12. The method of claim 8 or claim 9 , wherein the activated regulatory T-cells are separated after stimulation of cells in the cell mixture.
13. The method of claim 1 , wherein the separation is performed by flow-cytometry or magnetic cell sorting.
14. The method of claim 1 , wherein the molecule binding CD154 is coupled to a fluorescent dye, a hapten and/or a magnetic particle.
15. The method of claim 2 or claim 3 , wherein the molecule binding the additional marker is coupled to a fluorescent dye, a hapten and/or a magnetic particle.
16. The method of claim 1 , wherein the additional marker is CD25.
17. The method of claim 1 , wherein the additional marker is CD137.
18. The method of claim 1 , wherein the enriched cell population is enriched for cells that are specific for a particular antigen.