IP Library › Granted Patent US 9,023,355
Granted Patent B2
US 9,023,355 · App. 13/404,725 · Granted May 5, 2015

Compositions and methods for treating renal disease

Inventors: David J. Friedman (Boston, MA); Martin R. Pollak (Boston, MA)
Assignee: Beth Israel Deaconess Medical Center, Inc.
G01N33/92G01N33/6893G01N2333/16G01N2800/347G01N2800/50C12Q1/6883C12Q2600/156C07K16/18
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Quick Facts
Patent No.
US 9,023,355
App. No.
13/404,725
Granted
May 5, 2015
Kind
B2
Abstract

Compositions and methods are disclosed herein for treating or reducing the symptoms of a renal disease, such as focal segmental glomerulosclerosis (FSGS), hypertensive end-stage kidney disease (ESKD), and HIV-associated nephropathy (a distinct form of FSGS, also termed collapsing glomerulopathy). The compositions include the common variant of APOL1 and fragments thereof, as well as antibodies and fragments thereof that bind and neutralize pathogenic APOL1, nucleic acid molecules that encode the common variant of APOL1 and fragments thereof, and other compounds that bind and neutralize pathogenic APOL1. The methods of the invention include administering one or more of the compositions of the invention to a subject having or at risk of developing renal disease.

Claims (9)

1. A method of treating or reducing the likelihood of development of a renal disease comprising administering to a human subject expressing at least one pathogenic human APOL1 polypeptide comprising an S342G substitution, an I384M substitution, or a deletion removing amino acids N388 and Y389 a composition comprising an anti-APOL1 antibody or fragment thereof that specifically binds to the pathogenic APOL1 polypeptide, but does not specifically bind, or binds at a substantially greater dissociation constant, to a non-pathogenic APOL1 polypeptide, wherein said composition decreases a deleterious effect of the pathogenic APOL1 polypeptide.

2. The method of claim 1 , wherein said anti-APOL1 antibody or fragment thereof neutralizes said human pathogenic APOL1 polypeptide.

3. The method of claim 1 , wherein said composition treats or substantially inhibits development of said renal disease or treats or reduces one or more symptoms associated with said renal disease.

4. The method of claim 1 , wherein said renal disease glomerulosclerosis.

5. The method of claim 1 further comprising, prior to administering said inhibitor, determining the expression of at least one pathogenic APOL1 polypeptide in said subject.

6. The method of claim 5 , wherein the subject is homozygous or heterozygous for at least one or more APOL1 alleles that encode said pathogenic APOL1 polypeptide.

7. The method of claim 1 , wherein the subject is an African-American subject.

8. The method of claim 1 further comprising administering to said subject a therapeutic agent selected from the group consisting of a blood pressure medication and a cholesterol-lowering medication.

9. The method of claim 1 , wherein said renal disease is selected from the group consisting of focal segmental glomerulosclerosis (FSGS), end-stage kidney disease (ESKD), hypertensive ESKD, idiopathic nephritic syndrome, and human immunodeficiency virus (HIV)-associated nephropathy.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 16, 2012
From: FRIEDMAN, DAVID J.; POLLAK, MARTIN R.
To: BETH ISRAEL DEACONESS MEDICAL CENTER, INC.
Reel/Frame 028217/0470 →
Continuity (6)
Continuation In Part PCTUS2011032924 · Apr 18, 2011
Continuation In Part PCTEP2010062065 · Aug 18, 2010
Provisional Application 61489140 · May 23, 2011
Provisional Application 61325343 · Apr 18, 2010
Provisional Application 61323727 · Apr 13, 2010
Related Publication 20120195902A1 · Aug 2, 2012