Inhibition of vascular smooth muscle cell proliferation with implanted matrix containing vascular endothelial cells

• US 5,766,584 A
• Filed: 06/02/1995
• Issued: 06/16/1998
• Est. Priority Date: 06/02/1995
• Status: Expired due to Term

• Current Assignee: Massachusetts Institute of Technology
• Original Assignee: Massachusetts Institute of Technology
• Inventors: Nathan, Aruna, Nugent, Matthew A., Edelman, Elazer R.
• Primary Examiner(s): Naff, David M.
• Application Number:
  US08/458,978
• Time in Patent Office: 1,110 Days
• Field of Search: 435/174, 435/177, 435/180, 435/182, 435/240.23, 435/395, 435/397, 435/398, 435/402, 424/93.7, 424/422, 424/423, 424/425, 424/426, 514/56
• US Class Current: 424/93.7
• 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: A61L 27/507 for artificial blood vessels apparatus for applying cells on a blood vessel prosthesis A61F2/062
• CPC Class Codes: A61L 31/005 Ingredients of undetermined constitution or reaction products thereof
• CPC Class Codes: A61P 9/10 for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
• CPC Class Codes: C12N 2533/54 Collagen; Gelatin
• CPC Class Codes: C12N 5/069 Vascular Endothelial cells

Abstract

A composition and method are provided for inhibition of vascular smooth muscle cell proliferation following injury to the endothelial cell lining of a blood vessel such as resulting from angioplasty, vascular bypass surgery or organ transplantation. The composition is a matrix such as a biodegradable hydrogel made of a synthetic polymer, protein or polysaccharide seeded with vascular endothelial cells which can be xenografts, allografts or autografts, or genetically engineered cells. Attachment of cells to the matrix can be enhanced by coating with collagen, laminin, fibronectin, fibrin, basement membrane components or attachment peptides. Biologically active compounds such as anti-inflammatory agents may also be contained in the matrix. In the method, the matrix containing endothelial cells is implanted in a patient at a site adjacent the injury such as by wrapping the matrix around the blood vessel. The endothelial cells secrete products that diffuse into surrounding tissue but do not migrate to the endothelial cell lining of the blood vessel. The endothelial cells may be obtained by biopsy of the patient into which the matrix is implanted and the cells can be cultured in the matrix in vitro and then implanted in vivo.

Claims

1. A method of inhibiting mechanisms involved in restenosis of a blood vessel having an endothelial cell lining following injury to the endothelial cell lining of the blood vessel of a patient in need of treatment thereof comprising:

implanting a biocompatible matrix having seeded therein or thereon dissociated vascular endothelial cells at a site adjacent to the injury to the endothelial cell lining, wherein the vascular endothelial cells are provided in an amount effective to inhibit smooth muscle cell proliferation at the site of the injury without migration of the vascular endothelial cells to the endothelial cell lining of the blood vessel.

2. The method of claim 1 wherein the injury arises from angioplasty, coronary artery bypass surgery, peripheral bypass surgery, or organ transplantation.

3. The method of claim 1 wherein the matrix is in a form selected from the group consisting of gels, foams, suspensions, microcapsules, solid polymeric supports, and fibrous structures.

4. The method of claim 1 wherein the cells are obtained by biopsy of the patient into which the matrix is implanted.

5. The method according to claim 1 wherein the matrix is biodegradable.

6. The method of claim 5 wherein the matrix is formed of a material selected from the group consisting of polyhydroxy acids, polyorthoesters, polyanhydrides, proteins, polysaccharides, polyphosphazenes, polyalkylene oxides and combinations thereof.

7. The method of claim 1 wherein the matrix is formed of a material selected from the group consisting of ethylene vinyl acetate, polyvinyl alcohol, silicone, polyurethane, non-biodegradable polyesters, polyethyleneoxide-polypropyleneoxide, tetrafluoroethylene and combinations thereof.

8. The method of claim 1 wherein the matrix further comprises biologically active compounds selected from the group consisting of prostaglandins, prostanoids, tyrosine kinase inhibitors, immunosuppressants, glucocorticoids, anti-oxidants, free radical scavengers, peptide hormones, angiogenic factors, angiogenic inhibitory factors, and combinations thereof.

9. The method of claim 1 wherein the cells are first cultured in the matrix in vitro, then implanted in vivo.

10. The method of claim 1 wherein the matrix is surgically implanted around the blood vessel.

15. The composition according to claim 4 wherein the matrix is biodegradable.

16. The composition of claim 15 wherein the matrix is formed of a material selected from the group consisting of polyhydroxy acids, polyorthoesters, polyanhydrides, proteins, polysaccharides, polyphosphazenes, and combinations thereof.

11. A composition for inhibiting mechanisms involved in restenosis of a blood vessel having an endothelial cell lining following injury to the endothelial cell lining of the blood vessel in a patient in need of treatment thereof, comprising a biocompatible matrix shaped for implantation adjacent to a blood vessel, the matrix having seeded therein or thereon dissociated vascular endothelial cells, wherein the vascular endothelial cells are in an amount effective to inhibit smooth muscle cell proliferation at the site of the injury without migration of the vascular endothelial cells to the endothelial cell lining of the blood vessel.

12. The composition of claim 11 wherein the amount is effective to treat an injury arising from angioplasty, coronary artery bypass surgery, peripheral bypass surgery, or organ transplantation.

13. The composition of claim 11 wherein the matrix is in a form selected from the group consisting of gels, foams, suspensions, microcapsules, solid polymeric supports, and fibrous structures.

14. The composition of claim 11 wherein the cells are selected from the group consisting of autologous cells, allograft cells, and xenograft cells.

17. The composition of claim 11 wherein the matrix is formed of a material selected from the group consisting of ethylene vinyl acetate, polyvinyl alcohol, silicone, polyurethane, non-biodegradable polyesters, polyethyleneoxide-polypropyleneoxide, tetrafluoroethylene, and combinations thereof.

18. The composition of claim 11 wherein the matrix further comprises biologically active compounds selected from the group consisting of prostaglandins, prostanoids, tyrosine kinase inhibitors, immunosuppressants, glucocorticoids, anti-oxidants, free radical scavengers, peptide hormones, angiogenic factors, angiogenic inhibitory factors, and combinations thereof.

19. The composition of claim 14 wherein the cells are genetically engineered.