In vitro micro-organs, and uses related thereto

• US 20030152561A1
• Filed: 12/17/2002
• Published: 08/14/2003
• Est. Priority Date: 01/09/1998
• Status: Active Grant

• Current Assignee: Eduardo N. Mitrani
• Original Assignee: Eduardo N. Mitrani
• Inventors: Mitrani, Eduardo N.
• Granted Patent: US 7,687,057 B2
• Time in Patent Office: Days
• US Class Current: 424/93.21
• CPC Class Codes: A61M 1/1678 intracorporal peritoneal dialysis A61M1/28
• CPC Class Codes: A61M 1/34 Filtering material out of the blood by passing it through a membrane, i.e. hemofiltration or diafiltration
• CPC Class Codes: A61M 1/3489 by biological cells, e.g. bioreactor

Abstract

A method of delivering a gene product to a recipient, the method comprises (a) providing a micro-organ explant expressing at least one recombinant gene product, the micro-organ explant comprising a population of cells, the micro-organ explant maintaining a microarchitecture and a three dimensional structure of an organ from which it is obtained and at the same time having dimensions selected so as to allow diffusion of adequate nutrients and gases to cells in the micro-organ explant and diffusion of cellular waste out of the micro-organ explant so as to minimize cellular toxicity and concomitant death due to insufficient nutrition and accumulation of the waste in the micro-organ explant, at least some of the cells of the population of cells of the micro-organ explant expressing at least one recombinant gene product; and (b) implanting the micro-organ explant in the recipient.

Claims

1. A method of delivering a gene product to a recipient, the method comprising the steps of:

(a) providing a micro-organ explant expressing at least one recombinant gene product, the micro-organ explant comprising a population of cells, the micro-organ explant maintaining a microarchitecture and a three dimensional structure of an organ from which it is obtained and at the same time having dimensions selected so as to allow diffusion of adequate nutrients and gases to cells in the micro-organ explant and diffusion of cellular waste out of the micro-organ explant so as to minimize cellular toxicity and concomitant death due to insufficient nutrition and accumulation of the waste in the micro-organ explant, at least some of the cells of said population of cells of the micro-organ explant expressing at least one recombinant gene product; and

(b) implanting the micro-organ explant in the recipient.

2. The method of claim 1, wherein said micro-organ explant is derived from the recipient.

3. The method of claim 1, wherein said micro-organ explant is derived from a donor subject.

4. The method of claim 1, wherein said micro-organ explant is derived from a human being.

5. The method of claim 1, wherein said micro-organ explant is derived from a non-human animal.

6. The method of claim 1, wherein the recipient is a human being.

7. The method of claim 1, wherein the recipient is a non-human animal.

8. The method of claim 1, wherein said at least one recombinant gene product is selected from the group consisting of a recombinant protein and a recombinant functional RNA molecule.

9. The method of claim 8, wherein said recombinant protein is normally produced by the organ from the micro-organ explant is derived.

10. The method of claim 8, wherein said recombinant protein is normally not produced by the organ from which the micro-organ explant is derived.

11. The method of claim 8, wherein said recombinant protein is selected from the group consisting of a protease, a lipase, a ribonuclease, a deoxyribonuclease, a blood clotting factor, a cytochrome p450 enzyme, a transcription factor and a MHC component.

12. The method of claim 8, wherein said recombinant protein is selected from the group consisting of a peptide, a glycoprotein and a lipoprotein.

13. The method of claim 8, wherein said recombinant protein is selected from the group consisting of insulin, trypsinogen, chymotrypsinogen, carboxypeptidase, triaclyglycerol lipase, phospholipase A₂, elastase, amylase, UDP glucuronyl transferae, ornithine transcarbanoylase, adenosine deaminase, serum thymic factor, thymic humoral factor, thymopoietin, thymosin (α

₁, gastrin, secretin, cholecystokinin, somatostatin, substance P and growth hormone.

14. The method of claim 1, wherein said genetically modified micro-organ transplant is maintainable in culture for at least about twenty-four hours.

15. The method of claim 1, wherein said genetically modified micro-organ transplant has a surface area to volume index characterized by the formula 1/x+1/a>

1.5 mm<sup>−

1</sup>;

wherein ‘

x’

is a tissue thickness and ‘

a’

is a width of said tissue in millimeters.

16. The method of claim 1, wherein said organ is selected from the group consisting of a lymph organ, a pancreas, a liver, a gallbladder, a kidney, a digestive tract organ, a respiratory tract organ, a reproductive organ, skin, a urinary tract organ, a blood-associated organ, a thymus, a spleen.

17. The method of claim 1, wherein said genetically modified micro-organ transplant comprising epithelial and connective tissue cells, arranged in a microarchitecture similar to the microarchitecture of the organ from which the explant was obtained.

18. The method of claim 1, wherein the organ is a pancreas, and the population of cells includes islets of Langerhans.

19. The method of claim 1, wherein the organ is skin, and the explant includes at least one hair follicle and at least one gland.

20. The method of claim 1, wherein the organ is a diseased skin, and the explant includes a population of hyperproliferative or neoproliferative cells from the diseased skin.

21. The method of claim 1, wherein said genetically modified micro-organ transplant is maintainable in a minimal medium.

22. The method of claim 1, wherein the explant is maintainable in an artificial medium.

23. The method of claim 1, wherein the explant is maintainable in a defined medium.

24. The method of claim 1, wherein the retained microarchitecture of the genetically modified micro-organ transplant comprises one or more cell-cell and cell-matrix orientations between two or more tissues of the organ from which the explant is isolated.

25. The method of claim 1, wherein at least a portion of the population of cells is transduced, transformed or transfected with a recombinant construct carrying a recombinant gene encoding said recombinant gene product.

26. The method of claim 25, wherein said recombinant construct is a virus vector selected from the group consisting of a recombinant hepatitis virus, a recombinant adeno virus, a recombinant adeno-associated virus, a recombinant papilloma virus, a recombinant retrovirus, a recombinant cytomegalovirus and a recombinant simian virus.

27. The method of claim 25, wherein said recombinant construct is a naked nucleic acid molecule.

28. The method of claim 1, wherein at least a portion of the population of cells are transformed with a foreign nucleic acid sequence via a transformation method selected from the group consisting of calcium-phosphate mediated transfection, DEAE-dextran mediated transfection, electroporation, liposome-mediated transfection, direct injection, and receptor-mediated uptake.

29. The method of claim 1, further comprising the step of encapsulating said genetically modified micro-organ culture prior to said step (c).

30. The method of claim 1, wherein step (a) is effected by:

(i) isolating from an animal a portion of an organ including the population of cells, the portion of the organ maintaining a microarchitecture and a three dimensional structure of an organ from which it is obtained and at the same time having dimensions selected so as to allow diffusion of adequate nutrients and gases to cells in the micro-organ explant and diffusion of cellular waste out of the micro-organ explant so as to minimize cellular toxicity and concomitant death due to insufficient nutrition and accumulation of the waste in the micro-organ explant; and

(ii) genetically modifying at least some of the cells of said population of cells of the portion of the organ with a recombinant gene to express at least one recombinant gene product.

31. The method of claim 1, wherein said step (a) is effected by obtaining said micro-organ explant from an organ of a transgenic animal expressing said recombinant gene product.