IP Library Granted Patent US 7,803,981
Granted Patent B2
US 7,803,981 · App. 11/820,768 · Granted Sep 28, 2010

Transgenic ungulates capable of human antibody production

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Quick Facts
Patent No.
US 7,803,981
App. No.
11/820,768
Granted
Sep 28, 2010
Kind
B2
Abstract

The invention features novel methods for the production of large quantities of xenogenous antibodies, such as human antibodies. Preferably, this result is effected by inactivation of IgM heavy chain expression and, optionally, by inactivation of Ig light chain expression, and by the further introduction of an artificial chromosome which results in the expression of xenogenous antibodies (e.g., non-bovine antibodies), preferably human antibodies.

Claims (20)

1. A transgenic ungulate whose genome comprises a mutation in an endogenous immunoglobulin (Ig) heavy chain or Ig light chain locus, said mutation reducing the expression of said Ig heavy chain or Ig light chain.

2. The ungulate of claim 1 , wherein said mutation reduces the expression of functional IgM heavy chain.

3. The ungulate of claim 1 , wherein said mutation substantially eliminates the expression of said Ig heavy chain or said Ig light chain.

4. The ungulate of claim 1 , wherein said mutation is hemizygous.

5. The ungulate of claim 1 , wherein said mutation is homozygous.

6. The ungulate of claim 1 , wherein said mutation is an insertion of a positive selection marker into said endogenous locus.

7. The ungulate of claim 6 , wherein said positive selection marker is an antibiotic resistance gene.

8. The ungulate of claim 7 , wherein each allele comprises the same antibiotic resistance gene.

9. The ungulate of claim 7 , wherein each allele comprises a different antibiotic resistance gene.

10. The ungulate of claim 6 , wherein said positive selection marker is operably linked to a xenogenous promoter.

11. The ungulate of claim 1 , wherein said mutation is an insertion of a transcription termination sequence into said endogenous loci.

12. The ungulate of claim 11 , wherein said transcription termination sequence is inserted downstream of the initial ATG codon in exon 2 of an endogenous mu heavy chain locus.

13. The ungulate of claim 1 , comprising one or more nucleic acids comprising one or more transgenes and expressing an mRNA or protein encoded by said transgene(s).

14. The ungulate of claim 1 , wherein said ungulate is a pig.

15. An isolated ungulate somatic cell comprising a mutation in an endogenous immunoglobulin (Ig) heavy chain or Ig light chain locus, said mutation reducing the expression of said Ig heavy chain or Ig light chain.

16. The cell of claim 15 , comprising a mutation in both alleles of said IgM heavy chain or said light chain.

17. The cell of claim 15 , wherein said mutation is a transcription termination sequence.

18. The cell of claim 17 , wherein said transcription termination sequence is inserted downstream of the initial ATG codon in exon 2 of an endogenous mu heavy chain locus.

19. The cell of claim 15 , wherein said cell is a fetal fibroblast or a B-cell.

20. The cell of claim 15 , wherein said ungulate is a pig.

Assignments (6)
CHANGE OF NAME Recorded Jan 12, 2015
From: SANFORD APPLIED BIOSCIENCES, L.L.C.
To: SAB, LLC
Reel/Frame 034751/0027 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 8, 2013
From: KYOWA HAKKO KIRIN CO., LTD.
To: SANFORD APPLIED BIOSCIENCES, L.L.C.
Reel/Frame 029951/0691 →
CHANGE OF NAME Recorded Dec 19, 2012
From: KIRIN PHARMA KABUSHIKI KAISHA
To: KYOWA HAKKO KIRIN CO., LTD.
Reel/Frame 029500/0933 →
MERGER Recorded Mar 26, 2009
From: KIRIN PHARMA KABUSHIKI KAISHA
To: KYOWA HAKKO KIRIN CO., LTD.
Reel/Frame 022455/0852 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 20, 2009
From: GOLDSBY, RICHARD A.; OSBORNE, BARBARA
To: KIRIN PHARMA KABUSHIKI KAISHA
Reel/Frame 022428/0439 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2007
From: ROBL, JAMES M.; COLLAS, PHILIPPE; SULLIVAN, EDDIE; KASINATHAN, POOTHAPPILLAI; KUROIWA, YOSHIMI; TOMIZUKA, KAZUMA; ISHIDA, ISAO
To: KIRIN PHARMA KABUSHIKI KAISHA
Reel/Frame 020007/0968 →