In vivo bioreactors

• US 20050079159A1
• Filed: 06/13/2002
• Published: 04/14/2005
• Est. Priority Date: 06/13/2001
• Status: Abandoned Application

• Current Assignee: Massachusetts Institute of Technology
• Original Assignee: Massachusetts Institute of Technology
• Inventors: Shastri, Venkatram Prasad, Langer, Robert S, Stevens, Molly M
• Application Number:
  US10/480,682
• Publication Number:
  US 20050079159A1
• Time in Patent Office: Days
• US Class Current: 424/93.700
• CPC Class Codes: A01K 67/0271 Chimeric vertebrates, e.g. comprising exogenous cells
• CPC Class Codes: A61K 31/70 Carbohydrates; Sugars; Derivatives thereof sorbitol A61K31/047
• CPC Class Codes: A61K 35/12 Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells vaccines or medicinal preparations containing antigens or antibodies A61K39/00
• CPC Class Codes: A61P 43/00 Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• CPC Class Codes: C12N 2501/115 Basic fibroblast growth factor (bFGF, FGF-2)
• CPC Class Codes: C12N 2501/15 Transforming growth factor beta (TGF-β)
• CPC Class Codes: C12N 2533/40 Polyhydroxyacids, e.g. polymers of glycolic or lactic acid (PGA, PLA, PLGA); Bioresorbable polymers
• CPC Class Codes: C12N 2533/74 Alginate
• CPC Class Codes: C12N 5/0068 General culture methods using substrates for specific animal cell type C12N5/06
• CPC Class Codes: C12N 5/0654 Osteocytes, Osteoblasts, Odontocytes; Bones, Teeth
• CPC Class Codes: C12N 5/0655 Chondrocytes; Cartilage

Abstract

The present invention relates to an in vivo method of promoting the growth of autologous tissue and its use to form corrective structures, including tissue that can be explanted to other locations in the animal. In particular, the invention relates to methods and systems for (a) the site-specific regeneration of tissue, and (b) the synthesis of neotissue for transplantation.

Claims

1. A method for promoting generation of soft tissue, or precursor cells for soft tissue, comprising the steps of:

i. creating an artificial space or environment in an organ or cavity of an animal; and

ii. introducing into the artificial space a matrix which is conducive to infiltration by, and growth and/or differentiation of pluripotent cells from the tissue surrounding the artificial space.

2. The method of claim 1, including the further step of harvesting the pluripotent cells, or tissue derived therefrom, from the artificial space.

3. The method of claim 2, wherein the harvested cells are reimplanted in the animal.

4. The method of claim 1, wherein the artificial space is created in or adjacent periosteum tissue.

5. The method of claim 1, wherein the artificial space is created between a mesenchymal portion of a soft tissue organ and an adjacent epithelium or compact mesenchymal layer of the organ.

6. The method of claim 1, wherein the tissue is selected from the group consisting of liver, pancreas, kidney, muscle, spleen, teeth, dentin, mucosa and bone.

7. The method of claim 1, wherein the artificial space is created with retractor having a fluid-operated portion, such as a balloon or bladder, to retract a portion of the soft tissue.

8. The method of claim 1, wherein the area in which the artificial space is to be created is treated with an agent to partially degrade the connective tissue at the site, freeing cells to promote formation of the space and/or promote migration of cells into the space.

9. The method of claim 7, wherein the agent is selected from the group consisting of trypsin, chymotrypsin, collagenase, elastase, hyaluronidase, pronase and chondroitinase.

10. The method of claim 1, wherein the matrix is a porous, biodegradable polymer.

11. The method of claim 1, wherein the matrix is a solution at the time of injection into the artificial space or environment, but which gains dimensional stability in situ.

12. The method of claim 1, wherein the matrix is a hydrogel.

13. The method of claim 12, wherein the hydrogels is selected from the group consisting of a Pluronics hyrgogel, an alginates, a hydrogel formed from polyethylene glycol polylactic acid copolymers, and a Tetronics hydrogel.

14. The method of claim 1, wherein the matrix includes appropriate nutrients for promoting growth of said infiltrating cells.

15. The method of claim 1, wherein the matrix includes one or more growth factors for promoting growth and/or differentiation of said infiltrating cells.

16. The method of claim 15, wherein said one or more growth factors are selected from the group consisting of basic fibroblast growth factor (bFGF, or FGF-2), acid fibroblast growth factor (aFGF), epidermal growth factor (EGF), heparin binding growth factor (HBGF), fibroblast growth factor (FGF), vascular endothelium growth factor (VEGF), transforming growth factor (including TGF-α

, TGF-β

, and bone morphogenic proteins such as BMP-2, -3, -4, -7), Wnts, hedgehogs (including sonic, indian and desert hedgehogs), transforming growth factor-(x (TGF-α

), noggin, activins, inhibins, insulin-like growth factor (such as IGF-I and IGF-II), growth and differentiation factors 5, 6, or 7 (GDF 5, 6,

     7), leukemia inhibitory factor (LIF/HILDA/DIA), Wnt proteins, platelet-derived growth factors (PDGF), vitronectin (VN), laminin (LN), bone sialoprotein (BSP), and osteopontin (OPN), parathyroid hormone related polypeptide (PTHrP), and the like.

17. The method of claim 1, wherein the matrix includes one or more anti-angiogenic agents.

18. The method of claim 1, wherein the matrix includes one or more extracellular matrix proteins selected from the group consisting of collagen, chondronectin, fibronectin, vitronectin, proteoglycans, and glycoasminoglycans chains.

19. The method of claim 1, wherein the matrix includes is a composite of naturally and artificial polymers.

20. The method of claim 1, wherein the biodegradable matrix includes a chemotactic substance for promoting migration of said infiltrating cells into said artificial space.

21. The method of claim 1, wherein the shields and/or spacers are placed in the artificial space.

32. A method of conducting a regenerative medicine business, comprising:

a. providing instruction for carrying out the method of claim 1 or 22 to isolate cells or tissue from a patient; and

b. providing a cell banking services for preserving the isolated cells or tissue.

33. A method of conducting a regenerative medicine business, comprising:

a. providing instruction for carrying out the method of claim 1 or 22 to isolate cells or tissue from a patient; and

b. providing a services for further processing the isolated cells or tissue, as for example, to expand the cell population or differentiate the cells.

22. A method for promoting generation of cartilage or bone tissue, comprising the steps of:

i. creating an artificial space in or adjacent periosteum tissue of an animal; and

ii. introducing into the artificial space a porous, biodegradable polymer matrix which is compatible with growth of chondrocytes from the periosteum surrounding the artificial space.

23. The method of claim 22, wherein the biodegradable matrix includes appropriate nutrients for promoting growth of said chondrocytes.

24. The method of claim 22, wherein the biodegradable matrix includes one or more growth factors for promoting growth of said chondrocytes.

25. The method of claim 24, wherein said growth factors are selected from the group consisting of a somatomedin, a hedgehog protein, parathyroid related hormone, a basic fibroblast growth factor, a transforming growth factor-β

, a cartilage growth factor, and combinations thereof.

26. The method of claim 25, wherein the biodegradable matrix includes one or more anti-angiogenic agents.

27. The method of claim 22, wherein the artificial space is treated with an agent to partially degrade the connective tissue at the site, freeing cells to promote formation of the space and/or promote migration of cells into the space.

28. The method of claim 27, wherein the agent is selected from the group consisting of trypsin, chymotrypsin, collagenase, elastase, hyaluronidase, pronase and chondroitinase.

29. A kit for promoting generation of tissue in vivo, comprising:

a. a tissue retractor for generating the artificial space;

b. a matrix which is conducive to infiltration by, and growth and/or differentiation of pluripotent cells; and

c. (optionally) an agent to partially degrade the connective tissue at the site, freeing cells to promote formation of the space and/or promote migration of cells into the space.

31. A method of conducting a regenerative medicine business, comprising:

a. marketing a kit of claim 29 or 30, and

b. providing instruction to customers purchasing the kit on how to use the kit for generating tissue in vivo.

30. A kit for promoting generation of tissue in vivo, comprising:

a. a matrix precursor(s) capable of forming a dimensionally stable matrix in vivo, which matrix is conducive to infiltration by, and growth and/or differentiation of pluripotent cells, which matrix precursor(s) is in the form of a solution;

b. a TGF-β and

b-FGF, admixed with said matrix precursor(s) or in a form which is amenable to mixture with said matrix precursor(s); and

c. instructions (written or pictorial) associated with said kit, said instructions describing the preparation of the matrix precursor(s), TGF-β and

b-FGF for injection into an artificial space or environment in vivo.