IP Library Granted Patent US 10,214,747
Granted Patent B2
US 10,214,747 · App. 15/110,200 · Granted Feb 26, 2019

Method of purifying monoclonal antibodies

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 10,214,747
App. No.
15/110,200
Granted
Feb 26, 2019
Kind
B2
Abstract

A new platform method to purify plant-based monoclonal antibodies is provided. Such a method includes an antibody purification platform that involves a standardized procedure for the production of a wide array of different antibodies within a simplified context. The versatility of the overall purification process accords a one-size-fits-all approach for myriad antibody products and includes plant tissue harvesting, extraction and clarification, filtrate generation, a succession of column chromatography procedures, and buffer exposure to provide the desired monoclonal antibodies in proper filtered and purified form for further incorporation and/or use within medicaments and other formulations. Thus, the purified monoclonal antibodies produced thereby such a method are also encompassed within this invention.

Claims (18)

1. A method of purifying monoclonal antibodies, following their production in a source organism, said method including the steps of:

a) harvesting monoclonal antibody sources from the source organism;

b) extracting said antibodies from said source organism and clarifying the antibodies;

c) processing said extracted and clarified antibodies through a series of chromatography separation procedures, i) wherein a first procedure includes an affinity column from which the target antibody is eluted with an arginine-containing acidic buffer to form an eluent containing full-length monomeric antibody structures, ii) wherein a second procedure includes an ion-exchange column for separating and collecting the full-length antibody monomeric structures from the eluent of step “c(i)”, and iii) wherein a third procedure includes a multimodal column from which the target antibody is eluted over a gradient established between at least one salt, during which the monomeric antibody structures are collected;

d) subjecting the collected antibody structures from step “c(iii)” to a buffer extraction step;

e) filtering said collected antibody structure fraction through a multiple filter press operation; and

f) collecting the resultant filtered monoclonal antibody formulations and storing the same for utilization as a bulk drug substance;

wherein extracting antibodies from said source organism in step “b” is performed with an extraction formulation comprising an alkaline buffer, an antioxidant and a chelating agent, and wherein before performing step “c(ii)” the antibody eluent of step “c(i)” is neutralized to a pH that is at least 0.2 units below the isoelectric point for the antibody.

2. The method of wherein said source organism is a plant.

3. The method of claim 2 wherein said harvesting step includes seed production and plant germination sub-steps followed by the inducement of transient gene expressions to form a specific protein associated with a desired monoclonal antibody, and then the growth of the resultant plant including the desired monoclonal source.

4. The method of claim 1 wherein the said monoclonal antibodies are immunoglobulin (IgG) antibodies.

5. The method of claim 1 wherein said method does not require any centrifugation steps for mAb extraction.

6. The method of claim 1 wherein step involves direct loading onto said affinity column and also wherein the gradient in step “c(iii)” is established between Sodium Phosphate-Sodium Chloride and the gradient is held once an absorbance reading exceeds 100 mAU.

7. The method of claim 1 , wherein monoclonal antibodies are generated from plants infiltrated with Agrobacterium lines separately containing expression constructs for each monoclonal antibody, one for heavy chain and the other for light chain production and wherein the method further comprises

incubating said infiltrated plants from 5 to 10 days post-infiltration to generate monoclonal antibody sources within source organisms present within said subject plants.

8. The method of claim 7 wherein said monoclonal antibodies are not subject to centrifugation for processing, clarifying, and/or extracting.

9. The method of claim 8 wherein said subject plants are provided from a master seed bank.

10. The method of claim 8 wherein said subject plants include Nicotiana benthamiana plants.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 4, 2026
From: KBIO HOLDINGS LIMITED
To: RP3 INC.
Reel/Frame 075523/0190 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 13, 2021
From: KENTUCKY BIOPROCESSING, INC.
To: KBIO HOLDINGS LIMITED
Reel/Frame 058372/0339 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 13, 2016
From: MORTON, JOSH; BRATCHER, BARRY; SWOPE, KELSI; HIATT, EMMETT ERNEST, III; HUME, STEVEN D.; ZEITLIN, LARRY
To: KENTUCKY BIOPROCESSING, INC.
Reel/Frame 039148/0825 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 13, 2016
From: MORTON, JOSH; BRATCHER, BARRY; SWOPE, KELSI; HIATT, ERNIE; HUME, STEVEN D.; ZEITLIN, LARRY
To: KENTUCKY BIOPROCESSING, INC.
Reel/Frame 039148/0858 →