← Back to Patent Explorer
US4652522A Expired / Lapsed US ⏱️ 0.0 years remaining

Continuous lymphocyte cell lines, their production and use

Assignee: University of Pennsylvania
•
Filing: 1983-07-05
•
Granted: 1987-03-24
•
Expires: 2003-07-05
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract A method for producing continuous B lymphocyte cell lines and monoclonal antibodies by such lines is provided. DNA isolated from neoplastic cells is introduced into stimulated lymphocytes. Individual cells that have been transformed by the added DNA and that produce antibodies are clonally expanded. Cultures of these continuous cells are employed to produce monoclonal antibodies.

Inventors

  • 👤 Roger H. Kennett
  • 👤 Zdenka L. Jonak

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 01:47
CPC Classifications
C; C12; C12N; C12N15/00; C12N15/09; C12N15/87; C07; C07K; C07K16/00; Y; Y10; Y10S; Y10S435/00; Y10S435/8215; Y10S435/948

Claims Analysis

Total Claims: 23
Claim 1
Independent Claim 65 words
A method of producing a continuous lymphocyte cell line comprising: (a) providing normal, stimulated B lymphocytes; (b) transfecting said lymphocytes with exogenous DNA isolated from a neoplastic cell, said DNA having the ability to transform lymphocytes; (c) recovering from said transfected lymphocytes a transformed lymphocyte; and (d) clonally expanding said transformed lymphocyte to a continuous cell line that stably maintains the production of monoclonal antibodies.
Claim 2
Independent Claim 65 words
A method of producing a continuous lymphocyte cell line comprising: (a) providing normal, stimulated B lymphocytes; (b) transfecting said lymphocytes with exogenous DNA isolated from a neoplastic cell, said DNA having the ability to transform lymphocytes; (c) recovering from said transfected lymphocytes a transformed lymphocyte; and (d) clonally expanding said transformed lymphocyte to a continuous cell line that stably maintains the production of monoclonal antibodies.
Claim 3
Dependent Claim 14 words
The method of claim 1 wherein said normal, stimulated B lymphocytes are human lymphocytes.
Claim 4
Dependent Claim 13 words
The method of claim 1 wherein said normal, stimulated lymphocytes are mouse lymphocytes.
Claim 5
Dependent Claim 13 words
The method of claim 1 wherein said neoplastic cell is a malignant lymphocyte.
Claim 6
Dependent Claim 13 words
The method of claim 2 wherein said neoplastic cell is a malignant lymphocyte.
Claim 7
Dependent Claim 13 words
The method of claim 3 wherein said neoplastic cell is a malignant lymphocyte.
Claim 8
Dependent Claim 14 words
The method of claim 1 wherein said neoplastic cell is a malignant B lymphocyte.
Claim 9
Dependent Claim 14 words
The method of claim 2 wherein said neoplastic cell is a malignant B lymphocyte.
Claim 10
Dependent Claim 14 words
The method of claim 3 wherein said neoplastic cell is a malignant B lymphocyte.
Claim 11
Dependent Claim 14 words
The method of claim 1 wherein said neoplastic cell is a Reh leukemia cell.
Claim 12
Dependent Claim 14 words
The method of claim 2 wherein said neoplastic cell is a Reh leukemia cell.
Claim 13
Dependent Claim 14 words
The method of claim 3 wherein said neoplastic cell is a Reh leukemia cell.
Claim 14
Dependent Claim 34 words
The method of claim 1 wherein said transfection comprises treatment of said normal, stimulated B lymphocytes with a calcium phosphate DNA coprecipitate in conjunction with treatment of said lymphocytes with polyethylene glycol and dimethylsulfoxide.
Claim 15
Dependent Claim 34 words
The method of claim 2 wherein said transfection comprises treatment of said normal, stimulated B lymphocytes with a calcium phosphate DNA coprecipitate in conjunction with treatment of said lymphocytes with polyethylene glycol and dimethylsulfoxide.
Claim 16
Dependent Claim 34 words
The method of claim 3 wherein said transfection comprises treatment of said normal, stimulated B lymphocytes with a calcium phosphate DNA coprecipitate in conjunction with treatment of said lymphocytes with polyethylene glycol and dimethylsulfoxide.
Claim 17
Dependent Claim 13 words
A continuous, stable, antibody-producing cell line produced by the method of claim 1.
Claim 18
Dependent Claim 13 words
A continuous, stable, antibody-producing cell line produced by the method of claim 2.
Claim 19
Dependent Claim 13 words
A continuous, stable, antibody-producing cell line produced by the method of claim 3.
Claim 20
Dependent Claim 18 words
A biologically pure culture of the continuous, stable, antibody-producing cell line produced by the method of claim 1.
Claim 21
Dependent Claim 23 words
A method of producing monoclonal antibodies comprising growing the cell line of claim 16 and recovering the antibodies produced by said cell line.
Claim 22
Dependent Claim 23 words
A method of producing monoclonal antibodies comprising growing the cell line of claim 17 and recovering the antibodies produced by said cell line.
Claim 23
Dependent Claim 23 words
A method of producing monoclonal antibodies comprising growing the cell line of claim 18 and recovering the antibodies produced by said cell line.

References Cited (Backward Citations)

US4001080A Cited
US4108983A Cited
US4195074A Cited
US4196265A Cited
US4172124A Cited
US4271145A Cited
US4332893A Cited
US4334016A Cited
EP0057107A2 Cited
US4565687A Cited
US4464465A Cited
US4529694A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-03-23 1990-09-22 1991-03-24 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-03-23 1994-09-22 1995-03-24 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-03-23 1998-09-22 1999-03-24 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag