Primed cell therapy
The subject invention is directed to a composition comprising primed connective tissue cells and a pharmaceutically acceptable carrier thereof.
1. A method of stimulating fibroblastic chondrocyte to gain chondrocytic characteristics in vitro comprising incubating the fibroblastic chondrocyte in a two-dimensional monolayer in a container coated with collagen with a composition consisting essentially of an active agent, which is TGF-β1 to create a primed cell, wherein the composition consists essentially of about 50 ng/ml TGF-β1.
2. The method of claim 1 , further comprising TGF-β3.
3. The method of claim 1 , further comprising BMP-2.
4. The method of claim 1 , further comprising fibroblast growth factor (FGF).
5. The method of claim 3 , further comprising insulin.
6. The method of claim 5 , further comprising T3.
7. A method of stimulating regeneration of cartilage at a target site in a mammal comprising injecting a therapeutically effective amount of the primed cell obtained in claim 1 into a target joint site where cartilage is desired to be generated, wherein endogenously existing forms of the connective tissue cells are decreased at the target site, and wherein the presence of the primed cells at the target site stimulates regeneration of cartilage.
8. The method according to claim 7 , wherein the subject suffers from degenerative arthritis.
9. The method according to claim 7 , wherein the target site is spinal column.
10. A method of stimulating regeneration of cartilage at a target site in a mammal comprising:
incubating a fibroblastic chondrocyte in a two-dimensional monolayer in a container coated with collagen with a composition consisting essentially of an active agent, which is TGF-β1 to create a primed cell, wherein the composition consists essentially of about 50 ng/ml TGF-β1; and
injecting a therapeutically effective amount of the obtained primed cell into a target joint site where cartilage is desired to be generated, wherein endogenously existing forms of the connective tissue cells are decreased at the target site, and wherein the presence of the primed cells at the target site stimulates regeneration of cartilage.
11. The method of claim 3 , wherein BMP-2 is about 200 ng/ml.
12. The method of claim 4 , wherein FGF is about 10 ng/ml.
13. The method of claim 5 , wherein insulin is about 15 pg/ml.
14. A method of stimulating fibroblastic chondrocyte to gain chondrocytic characteristics in vitro comprising incubating the fibroblastic chondrocyte in a two-dimensional monolayer in a container coated with collagen with a composition consisting essentially of an active agent, which is BMP-2 to create a primed cell, wherein the composition consists essentially of about 200 ng/ml BMP-2 and about 15 pg/ml insulin.
15. The method of claim 14 , wherein the composition further comprises TGF-β1.
16. The method of claim 14 , wherein the composition further comprises FGF.
17. The method of claim 14 , wherein the composition further comprises TGF-β3.
18. A method of stimulating regeneration of cartilage at a target site in a mammal comprising injecting a therapeutically effective amount of the primed cell obtained in claim 14 into a target joint site where cartilage is desired to be generated, wherein endogenously existing forms of the connective tissue cells are decreased at the target site, and wherein the presence of the primed cells at the target site stimulates regeneration of cartilage.
19. The method according to claim 18 , wherein the subject suffers from degenerative arthritis.
20. The method according to claim 18 , wherein the target site is spinal column.
21. A method of stimulating regeneration of cartilage at a target site in a mammal comprising:
incubating a fibroblastic chondrocyte in a two-dimensional monolayer in a container coated with collagen with a composition consisting essentially of an active agent, which is BMP-2 to create a primed cell, wherein the composition consists essentially of about 200 ng/ml BMP-2 and about 15 pg/ml insulin; and
injecting a therapeutically effective amount of the obtained primed cell into a target joint site where cartilage is desired to be generated, wherein endogenously existing forms of the connective tissue cells are decreased at the target site, and wherein the presence of the primed cells at the target site stimulates regeneration of cartilage.
22. The method of claim 14 , wherein the composition further comprises TGF-β1.
23. The method of claim 14 , wherein the composition further comprises FGF.
24. The method of claim 14 , wherein the composition further comprises TGF-β3.