IP Library Granted Patent US 8,790,666
Granted Patent B2
US 8,790,666 · App. 11/429,201 · Granted Jul 29, 2014

Nerve construct containing living stretch-grown nervous tissue

Inventor: Douglas H. Smith (Boothwyn, PA)
Assignee: The Trustees of the University of Pennsylvania
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Quick Facts
Patent No.
US 8,790,666
App. No.
11/429,201
Granted
Jul 29, 2014
Kind
B2
Abstract

The present invention relates to mechanically elongated neurons and provides useful compositions, devices and methods for treating a nerve lesion using such mechanically elongated neurons.

Claims (31)

1. A composition comprising:

a plurality of integrated neuronal cells, and

a biocompatible matrix,

wherein said plurality of integrated neuronal cells comprises two populations of cell bodies of mechanically elongated neurons, said two populations connected to each other by elongated fascicular axon tracts, and

wherein said mechanically elongated neurons are coated in said biocompatible matrix to form a sheet of matrix-coated integrated neuronal cells, such that said biocompatible matrix physically supports said mechanically elongated neurons and prevents damage to said axon tracts and wherein said sheet is rolled into a cylindrical shape.

2. The composition of claim 1 , wherein the mechanically elongated neurons are selected from the group consisting of a dorsal root ganglion (DRG) neuron, a sympathetic ganglion neuron, and a cortical neuron.

3. The composition of claim 2 , wherein the neurons are human neurons.

4. The composition of claim 1 , wherein the axons of the mechanically elongated neurons are elongated to at least 1 centimeter.

5. The composition of claim 4 , wherein the axons are elongated to at least 5 centimeters.

6. The composition of claim 1 , wherein the biocompatible matrix comprises a collagen hydrogel.

7. The composition of claim 1 , wherein the biocompatible matrix further comprises one or more neurotrophic factors.

8. The composition of claim 7 , wherein the one or more neurotrophic factors is selected from the group consisting of nerve growth factor (NGF), brain derived neurotrophic factor (BDNF), neurotrophin 3 (NT-3), neurotrophin 4/5 (NT-4/5), neurotrophin 6 (NT-6), neurotrophin 7 (NT-7), ciliary neurotrophic factor (CNTF), neurturin (NTN), persephin, artemin, basic fibroblastic growth factor (bFGF), glial-cell-derived neurotrophic factor (GDNF), purpurin and a synthetic neurotrophin.

9. The composition of claim 8 , wherein the one or more neurotrophic factor is nerve growth factor.

10. The composition of claim 1 , further comprising a sheath, wherein said sheath at least partially enfolds said composition.

11. A method of treating a nerve lesion in a subject, the method comprising administering to the subject a therapeutically effective amount of a composition comprising a plurality of integrated neuronal cells, and

a biocompatible matrix,

wherein said plurality of integrated neuronal cells comprises two populations of cell bodies of mechanically elongated neurons, said two populations connected to each other by elongated fascicular axon tracts, and

wherein said mechanically elongated neurons are coated in said biocompatible matrix to form a sheet of matrix-coated integrated neuronal cells, such that said biocompatible matrix physically supports said mechanically elongated neurons and prevents damage to said axon tracts and wherein said sheet is rolled into a cylindrical shape.

12. The method of claim 11 , wherein the mechanically elongated neurons are synapsed prior to administering the composition to the subject.

13. The method of claim 11 , wherein the mechanically elongated neurons are selected from the group consisting of a DRG neuron, a sympathetic ganglion neuron, and a cortical neuron.

14. The method of claim 13 , wherein the neurons are human neurons.

15. The method of claim 11 , wherein the mechanically elongated neurons are elongated to at least 1 centimeter.

16. The method of claim 11 , wherein the mechanically elongated neurons are is elongated to at least 5 centimeters.

17. The method of claim 11 , wherein the biocompatible matrix comprises a collagen hydrogel.

18. The method of claim 11 , wherein the biocompatible matrix further comprises one or more neurotrophic factors.

19. The method of claim 18 , wherein the one or more neurotrophic factors is selected from the group consisting of nerve growth factor (NGF), brain derived neurotrophic factor (BDNF), neurotrophin 3 (NT-3), neurotrophin 4/5 (NT-4/5), neurotrophin 6 (NT-6), neurotrophin 7 (NT-7), ciliary neurotrophic factor (CNTF), neurturin (NTN), persephin, artemin, basic fibroblastic growth factor (bFGF), glial-cell-derived neurotrophic factor (GDNF), purpurin and a synthetic neurotrophin.

20. The method of claim 19 , wherein the one or more neurotrophic factor is nerve growth factor.

21. The method of claim 11 , wherein the composition further comprises a sheath, wherein said sheath at least partially enfolds said composition.

22. The method of claim 11 , wherein the nerve lesion is in the central nervous system of the subject.

23. The method of claim 22 , wherein the nerve lesion is a spinal cord injury.

24. The method of claim 11 , wherein the subject is a human.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2013
From: SMITH, DOUGLAS H.
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 031790/0843 →
CONFIRMATORY LICENSE Recorded Jan 26, 2011
From: UNIVERSITY OF PENNSYLVANIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 025696/0649 →
Continuity (4)
Continuation In Part 10496476
Provisional Application 60336975 · Dec 4, 2001
Provisional Application 60386982 · Jun 6, 2002
Related Publication 20060292187A1 · Dec 28, 2006