Tolerogenic dendritic cells, method for their production and uses therof
The present invention relates to a tolerogenic dendritic cell population (Tr-DC) capable of generating a population of T cells having regulatory activity, method of production and uses thereof. Furthermore, soluble HLA-G promotes the differentiation of a population of T cells with regulatory activity.
1. An in vitro method for generating a population of human tolerogenic dendritic cells (Tr-DC) comprising the steps of:
a) collecting peripheral blood mononuclear cells (PBMCs) from a subject;
b) isolating adherent cells from collected PBMCs; and
c) exposing said isolated adherent cells at the start of culture on day 0 to an effective amount of GM-CSF, IL-4 and IL-10 to generate human Tr-DC,
wherein the generated human Tr-DC have a mature myeloid phenotype and have a marker phenotype comprising: CD14 + , CD11c + , CD11 b + , CD83 + , CD80 + , CD86 + , HLA-DR + , CD71 + and CD1a − ; wherein at least about 92% of the generated human Tr-DC are CD86 + positive.
2. The in vitro method according to claim 1 wherein said adherent cells are CD14 + monocytes.
3. The in vitro method according to claim 1 wherein the steps of isolating adherent cells and exposing said isolated adherent cells are performed in the presence of fetal calf serum (FCS) or of human serum (HS).
4. The in vitro method according to claim 1 wherein the effective amount of GM-CSF is between 1-1000 ng/ml.
5. The in vitro method according to claim 1 wherein the effective amount of IL-4 is between 1-1000 ng/ml.
6. The in vitro method according to claim 1 wherein the effective amount of IL-10 is between 1-1000 ng/ml.
7. The in vitro method of claim 1 , wherein the marker phenotype of the generated population of human tolerogenic Tr-DC further comprises: ILT-2 + and/or ILT-3 + and/or ILT-4 + and/or HLA-G + .
8. The in vitro method of claim 1 , wherein the generated population of human tolerogenic Tr-DC are capable of stimulating naive allogeneic CD4 + T cells, wherein the stimulated allogeneic CD4 + T cells, when activated, become Tr1 cells.
9. An in vitro method for generating a population of human tolerogenic dendritic cells (Tr-DC) comprising the steps of:
a) collecting peripheral blood mononuclear cells (PBMCs) from a subject;
b) isolating CD14 + cells from collected PBMCs; and
c) exposing said isolated CD14 + cells at the start of culture on day 0 to an effective amount of GM-CSF, IL-4 and IL-10 to generate human Tr-DC,
wherein the generated human Tr-DC have a marker phenotype comprising: CD14 + , CD11c + , CD11b + , CD80 + , and CD1a − ; and wherein at least about 92% of the generated human Tr-DC are CD86 + .
10. The in vitro method of claim 1 wherein the GM-CSF of step (c) is rhGM-CSF in a concentration of 100 ng/ml, the IL-4 of step (c) is rhIL-4 in a concentration of 10 ng/ml and the IL-10 of step (c) is rhIL-10 in a concentration of 10 ng/ml.
11. The in vitro method of claim 9 wherein the GM-CSF of step (c) is rhGM-CSF in a concentration of 100 ng/ml, the IL-4 of step (c) is rhIL-4 in a concentration of 10 ng/ml and the IL-10 of step (c) is rhIL-10 in a concentration of 10 ng/ml.
12. The in vitro method of claim 1 wherein the step of exposing said isolated adherent cells to an effective amount of GM-CSF, IL-4 and IL-10 is conducted for 7 days in the presence of DC medium.
13. The in vitro method of claim 9 wherein the step of exposing said isolated CD14 + cells to an effective amount of GM-CSF, IL-4 and IL-10 is conducted for 7 days in the presence of DC medium.
14. The in vitro method of claim 12 wherein the DC medium comprises RPMI 1640 supplemented with 10% FCS or 5% human serum, 100 U/ml penicillin/streptomycin and 50 μM 2 mercaptoethanol.
15. The in vitro method of claim 13 wherein the DC medium comprises RPMI 1640 supplemented with 10% FCS or 5% human serum, 100 U/ml penicillin/streptomycin and 50 μM 2 mercaptoethanol.