IP Library Granted Patent US 10,308,930
Granted Patent B2
US 10,308,930 · App. 15/514,052 · Granted Jun 4, 2019

Methods to accelerate antibody diversification

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,308,930
App. No.
15/514,052
Granted
Jun 4, 2019
Kind
B2
Abstract

Methods for increasing somatic hypermutation of antibodies, especially in vitro expression of an isolated retroviral protein in an isolated mammalian immunoglobulin-producing cell, are provided.

Claims (18)

1. A method of increasing somatic hypermutation of an immunoglobulin loci comprising effecting expression of a Tat protein in (i) an isolated mammalian immunoglobulin-producing cell, or (ii) an isolated immunoglobulin-producing cell of a cell line derived from a mammal, in an amount effective to increase somatic hypermutation of an immunoglobulin loci.

2. The method of claim 1 , wherein expression is effected in an isolated mammalian immunoglobulin-producing B cell.

3. The method of claim 1 , wherein expression is effected in the isolated immunoglobulin-producing cell of a cell line derived from a mammal.

4. The method of claim 3 , wherein the isolated immunoglobulin-producing cell of a cell line derived from a mammal is a cell that does not constitutively express immunoglobulins, but which has been genetically engineered to express immunoglobulins.

5. The method of claim 3 , wherein the isolated immunoglobulin-producing cell of a cell line derived from a mammal is a Ramos cell line.

6. The method of claim 1 , wherein the isolated immunoglobulin-producing cell of a cell line derived from a mammal is a hybridoma.

7. The method of claim 1 , wherein the cell secretes immunoglobulins.

8. The method of claim 1 , wherein the cell expresses immunoglobulins on a cell surface thereof.

9. The method of claim 1 , wherein the expression of the isolated exogenous protein is of a retroviral protein in the cell is effected by contacting the cell with a vector encoding the isolated retroviral protein.

10. The method of claim 1 , wherein the isolated retroviral protein is an HIV-2 Tat protein.

11. The method of claim 9 , wherein the vector is a lentiviral vector.

12. The method of claim 9 , wherein the vector is an adenoviral vector.

13. The method of claim 1 , wherein the expression of the HIV Tat protein in the cell is effected by contacting the cell with a pCDNA-tat eukaryotic expression vector encoding the exogenous HIV Tat protein.

14. The method of claim 1 , further comprising recovering one or more immunoglobulins produced by the cell of (i) or (ii) subsequent to effecting expression of the isolated exogenous protein therein.

15. The method of claim 14 , further comprising screening the one or more immunoglobulins for activity against a predetermined antigen.

16. The method of claim 1 , further comprising reducing expression of Spt5 in the cell of (i) by contacting the cell with a RNAi nucleic acid directed to Spt5.

17. The method of claim 16 , wherein the RNAi nucleic acid directed to Spt5 is a siRNA or an shRNA.

18. The method of claim 17 , wherein the RNAi nucleic acid is an shRNA delivered by a vector.

Assignments (1)
MERGER AND CHANGE OF NAME Recorded Feb 26, 2019
From: ALBERT EINSTEIN COLLEGE OF MEDICINE, INC.; ALBERT EINSTEIN COLLEGE OF MEDICINE
To: ALBERT EINSTEIN COLLEGE OF MEDICINE
Reel/Frame 048438/0275 →