IP Library Granted Patent US 8,105,594
Granted Patent B2
US 8,105,594 · App. 12/693,085 · Granted Jan 31, 2012

Methods for amyloid removal using anti-amyloid antibodies

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Quick Facts
Patent No.
US 8,105,594
App. No.
12/693,085
Granted
Jan 31, 2012
Kind
B2
Abstract

Methods and related immunoglobulin peptides and fragments thereof are disclosed that enhance the cell-mediated immune response of a patient to deposits of amyloid fibrils. These methods exploit the opsonizing effect of antibodies directed toward amyloid material or its component parts.

Claims (14)

1. A method of treating an amyloid deposition disease in a patient comprising administering to the patient at least one antibody or immunoglobulin polypeptide or fragment thereof which binds to human IgLC amyloid fibrils in an amount effective to enhance the cellular immune response of said patient to remove disease associated amyloid fibril deposits from said patient.

2. The method of claim 1 , wherein the antibody or immunoglobulin polypeptide or fragment thereof opsonizes said amyloid fibrils and induces removal of amyloid fibril deposits.

3. The method of claim 1 , wherein the antibody or immunoglobulin polypeptide or fragment thereof is a monoclonal antibody or fragment thereof.

4. The method of claim 3 , wherein the monoclonal antibody is selected from the group consisting of a humanized antibody, a chimeric antibody and a completely human antibody.

5. The method of claim 3 , wherein the monoclonal antibody is selected from the group consisting of κ1 (57-8H12), κ4 (11-1F4), λ8 (31-8C7) and combinations thereof.

6. The method of claim 3 , wherein the monoclonal antibody is selected from the group consisting of κ1 (57-8H12), κ4 (11-1F4), λ8 (31-8C7) and combinations thereof or a humanized or chimeric version of said monoclonal antibodies.

7. The method of claim 6 , wherein the monoclonal antibody is selected from the group consisting of a humanized antibody or a chimeric antibody.

8. The method of claim 1 , wherein the antibody is a labeled antibody.

9. The method of claim 1 , wherein the antibody or the immunoglobulin polypeptide or fragment thereof has been raised against an immunoglobulin light-chain.

10. The method of claim 1 , wherein the antibody or the immunoglobulin polypeptide or fragment thereof has been raised against synthetic amyloid fibrils.

11. The method of claim 1 , wherein the antibody or immunoglobulin polypeptide fragment is selected from the group consisting of a Fv fragment, Fab fragment, F(ab') fragment, F(ab') 2 fragment and ScFv fragment.

12. The method of claim 1 , wherein the antibody or the immunoglobulin polypeptide or fragment is a single chain antibody.

13. The method of claim 1 , wherein the antibody or the immunoglobulin polypeptide or fragment has cross-isotype reactivity.

14. The method of claim 1 , wherein the antibody or the immunoglobulin polypeptide or fragment is contained in a pharmaceutical composition further comprising a carrier.

Assignments (3)
CONFIRMATORY LICENSE Recorded Oct 19, 2016
From: UNIVERSITY OF TENNESSEE HEALTH SCI CTR
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 040417/0213 →
CHANGE OF NAME Recorded Apr 21, 2011
From: THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION
To: UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION
Reel/Frame 026160/0541 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2011
From: SOLOMON, ALAN; HRNCIC, RUDI; WALL, JONATHAN STUART
To: THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION
Reel/Frame 026143/0076 →
Continuity (3)
Continuation 09316387 · May 21, 1999
Provisional Application 60086198 · May 21, 1998
Related Publication 20100322932A1 · Dec 23, 2010