Myeloid Suppressor Cells, Methods For Preparing Them, and Methods For Using Them For Treating Autoimmunity
The present invention relates to novel myeloid suppressor cells (MSCs) and to methods of isolating these MSCs are also included. The MSCs of the present invention can be used to treat or prevent autoimmune diseases or alloimmune responses. The MSCs of the present invention may also be used to reduce a T cell response, induce T regulatory cells, and produce T cell tolerance.
1 . A method of treating an autoimmune disease in an individual, which method comprises administering a therapeutically effective amount of myeloid suppressor cells (MSCs) to the individual, wherein the MSCs have a Gr-1 + /CD11b + phenotype.
2 . The method according to claim 1 wherein the autoimmune disease is type I diabetes.
3 . The method according to claim 1 wherein the MSCs are autologous.
4 . The method according to claim 1 wherein the method further comprises administering an inhibitor of MSC terminal differentiation.
5 . The method according to claim 4 , wherein the inhibitor inhibits the activity of GM-CSF, M-CSF, or IL-3.
6 . The method according to claim 1 wherein the method further comprises altering SHIP signaling.
7 . The method according to claim 1 wherein the method further comprises increasing F4/80 expression.
8 . The method according to claim 1 , further comprising the step of administering one or more autoantigens.
9 . The method according to claim 1 wherein the MSCs are genetically modified to express or overexpress one or more autoantigens.
10 . The method according to claim 8 , which method further comprises administering a cytokine.
11 . The method according to claim 10 wherein the cytokine is IFN-γ, IL-10 or TGF-β.
12 . The method according to claim 1 wherein method further comprises administering an immunosuppressive drug.
13 . The method according to claim 12 wherein the immunosuppressive drug is cyclosporin, methotrexate, cyclophosphamide or tacrolimus.
14 . The method according to claim 1 , wherein the MSC phenotype further comprises CD115.
15 . The method according to claim 1 , wherein the MSC phenotype further comprises F4/80.
16 . The method according to claim 1 , wherein the phenotype includes at least one additional marker selected from the group consisting of CD31, c-kit, VEGF-receptor, and CD40.
17 . The method according to claim 1 , wherein the MSCs are genetically modified to overexpress Gr-1.
18 . The method according to claim 1 , wherein the MSCs are genetically modified to overexpress CD115.
19 . The method according to claim 1 , wherein the MSCs are genetically modified to overexpress F4/80.
20 . A method of treating an alloimmune response in an individual, which method comprises administering a therapeutically effective amount of myeloid suppressor cells (MSCs) to the individual, wherein the MSCs have a Gr-1 + /CD11b + phenotype.
21 . The method according to claim 20 wherein the alloimmune response is graft rejection.
22 . The method according to claim 20 wherein the alloimmune response is graft-versus-host disease (GVHD).
23 . The method according to claim 20 wherein the wherein MSCs are autologous.
24 . The method according to claim 20 wherein the method further comprises administering an inhibitor of MSC terminal differentiation.
25 . The method according to claim 24 wherein the inhibitor inhibits the activity of GMCSF, M-CSF, or IL-3.
26 . The method according to claim 20 wherein the method further comprises altering SHIP signaling.
27 . The method according to claim 20 wherein the method further comprises increasing F4/80 expression in MSCs.
28 . The method according to claim 20 , further comprising the step of administering one or more autoantigens.
29 . The method according to claim 20 wherein the MSCs express one or more autoantigens.
30 . The method according to claim 28 wherein method further comprises administering a cytokine.
31 . The method according to claim 30 wherein the cytokine is IFN-γ, IL-10 or TGF-β.
32 . The method according to claim 20 wherein method further comprises administering an immunosuppressive drug.
33 . The method according to claim 32 wherein the immunosuppressive drug is selected from the group consisting of cyclosporin, methotrexate, cyclophosphamide, and tacrolimus.
34 . The method according to claim 20 , wherein the MSC phenotype further comprises CD115.
35 . The method according to claim 20 , wherein the MSC phenotype further comprises F4/80.
36 . The method according to claim 20 , wherein phenotype includes at least one additional marker selected from the group consisting of CD31, c-kit, VEGF-receptor, and CD40.
37 . The method according to claim 20 , wherein the MSCs are genetically modified to overexpress Gr-1.
38 . The method according to claim 20 , wherein the MSCs are genetically modified to overexpress CD115.
39 . The method according to claim 20 , wherein the MSCs are genetically modified to overexpress F4/80.
40 . A method of producing myeloid suppressor cells (MSCs), which method comprises culturing primary hematopoietic stem cells (HSCs) in the presence of stem-cell factor (SCF) in an amount and for a time sufficient to allow HSCs to differentiate into MSCs, wherein the MSCs have a Gr-1 + /CD11b + phenotype.
41 . The method according to claim 40 , wherein the MSC phenotype further comprises CD115.
42 . The method according to claim 40 , wherein the MSC phenotype further comprises F4/80.
43 . The method according to claim 40 , wherein the phenotype includes at least one additional marker selected from the group consisting of CD31, c-kit, VEGF-receptor, and CD40.
44 . The method according to claim 40 , wherein the HSCs are genetically modified to overexpress Gr-1.
45 . The method according to claim 40 , wherein the HSCs are genetically modified to overexpress CD115.
46 . The method according to claim 40 , wherein the HSCs are genetically modified to overexpress F4/80.
47 . The method of claim 40 wherein the HSCs are further cultured in the presence of a factor selected from the group consisting of GM-CSF, M-CSF, G-CSF, Flit-3 ligand and tumor-conditioned medium.
48 . The method according to claim 40 , further comprising the step of isolating the MSCs.
49 . The method according to claim 48 wherein the step of isolating is by gradient centrifugation.