Gene transfer using transformed, neodetermined, embryonic cells

• US 5,032,407 A
• Filed: 01/16/1987
• Issued: 07/16/1991
• Est. Priority Date: 01/16/1987
• Status: Expired due to Fees

• Current Assignee: Ohio University Edison Animal Biotechnology Center A Branch of The State of Government of The State of Oh
• Original Assignee: Ohio University/Edison Animal Biotechnolgy Center
• Inventors: Reed, Michael A., Corn, Barbara J., Wagner, Thomas E.
• Primary Examiner(s): Weimar, Elizabeth C.
• Assistant Examiner(s): Chambers, Jasemine C.
• Application Number:
  US07/004,077
• Time in Patent Office: 1,642 Days
• Field of Search: 435/172.3, 435/240.2, 800/1, 800/2, 800/DIG. 2, 424/520, 424/582, 424/93, 935/62
• US Class Current: 800/23
• CPC Class Codes: A61K 48/00 Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
• CPC Class Codes: C12N 2510/00 Genetically modified cells
• CPC Class Codes: C12N 5/0603 Embryonic cells production of embryos, nuclear transfer A01K67/027; Embryoid bodies
• CPC Class Codes: C12N 5/0605 Cells from extra-embryonic tissues, e.g. placenta, amnion, yolk sac, Wharton's jelly

Abstract

This invention is directed to a method for the preparation of carrier cells capable of delivering exogenous genetic material to a particular tissue of the body by means of embryonic cells competent to develop into that tissue, and essentially only that tissue, said cells bearing the exogenous genetic material. The preferred carrier cells are mesodermal cells of the yolk sac or embryonic forebrain or midbrain cells, and the desired genetic material is preferably introduced into the cells by in vitro transformation with an amphotrophic retroviral vector.

Claims

1. A method of providing tissue-specific expression of exogenous genetic material is selected tissues of a recipient mammal which comprises:

(a) providing carrier cells capable of selectively delivering said exogenous genetic material to said tissues, said cells selected from the group consisting of embryonic yolk sac cells, embryonic midbrain cells and embryonic forebrain cells, all of which are derived from a donor mammal of the same species, said cells also having been transformed in vitro with said exogenous genetic material and

(b) introducing said cells into said recipient mammal in a manner permitting them to differentiate into said tissues.

2. The method of claim 1, where the carrier cells are mesodermal cells of the yolk sac which are competent to develop into hematopoietic stem cells, and the cells are introduced intravenously.

3. The method of claim 1, where the carrier cells are embryonic forebrain or midbrain cells.

4. The method of claim 1, where the cells are transformed with a retroviral vector carrying the genetic material.

5. The method of claim 4, where the retroviral vector is amphotrophic.

6. The method of claim 1 where the animal is immunocompetent and the introduction of the carrier cells does not result in an immune response.

7. The method of claim 1, said cells being essentially histocompatible with a host of the same species as the mammal from which the embryonic cells were derived.

8. The method of claim 1 in which the embryonic cells provided have been immortalized.

9. The method of claim 1, wherein the cells of the tissue are deficient in said genetic material.

10. The method of claim 1, where the cells are transformed by microinjecting them with the genetic material.

11. The method of claim 1 wherein the carrier cells are at a sufficiently early stage of development so that introduction of the carrier cells into an immunocompetent mammal does not result in an immune response to said carrier cells.

12. The method of claim 11 wherein the mammal is immunocompetent.

13. The method of claim 1 wherein the carrier cells are yolk sac cells derived from yolk sacs extracted from an embryonic donor mammal prior to the formation of blood islands visible at 12X magnification.

14. A process for producing a chimeric mammal characterized by the presence of heterologous genetic material in selected tissues of said mammal, which comprises introducing heterologous genetic material into said tissues by the method of claim 1.

15. The method of claim 1 wherein the carrier cells are provided in a non-enzymatically disaggregated form.