IP Library Patent Application 18512522
Patent Application
App. No. 18/512,522

MODULATING BONE MORPHOGENIC PROTEIN (BMP) SIGNALING IN THE TREATMENT OF ALZHEIMER'S DISEASE

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 None
App. No.
18/512,522
Abstract

Methods and compositions are provided for the treatment of Alzheimer's Disease (AD) by administering to a patient a therapeutically effective amount of an agent that inhibits signaling mediated by a bone morphogenetic protein type 1A receptor (BMPR-1A) or bone morphogenetic protein type 2 receptor (BMPR-2). Also provided are methods and compositions to increase the rate of neural stem cell self-renewal.

Claims (19)

1 . A method of treating a subject having Alzheimer's Disease (AD), the method comprising administering to the subject a therapeutically effective amount of an agent that inhibits signaling by BMPR 1A, BMPR 2, or both BMPR 1A and BMPR 2, wherein the agent is a nucleic acid, a protein, or an aptamer.

2 . A method of increasing a rate of self-renewal of a stem cell, the method comprising contacting the stem cell with an agent that inhibits signaling by BMPR 1A, BMPR 2, or both BMPR 1A and BMPR 2, wherein the agent is a nucleic acid, a protein, or an aptamer.

3 . The method of claim 1 , wherein the method is a method of increasing a rate of neural stem cell self-renewal in the subject.

4 . The method of claim 1 , wherein the agent:

(a) inhibits expression of a BMPR 1A mRNA or protein;

(b) binds a BMPR 1A protein; and/or

(c) inhibits interaction between a BMP protein and a BMPR 1A.

5 . The method of claim 1 , wherein the agent:

(a) inhibits expression of a BMPR 2 mRNA or protein;

(b) binds a BMPR 2 protein; and/or

(c) inhibits interaction between a BMP protein and a BMPR 2.

6 . The method of claim 1 , wherein the agent is the nucleic acid.

7 . The method of claim 6 , wherein the agent is a small interfering RNA (siRNA) or a short hairpin RNA (shRNA) that targets BMPR 1A, BMPR 2A, or both BMPR 1A and BMPR 2.

8 . The method of claim 6 , wherein the agent is an antisense oligonucleotide (ASO) that targets BMPR 1A, BMPR 2A, or both BMPR 1A and BMPR 2.

9 . The method of claim 6 , wherein the agent is a guide RNA (gRNA).

10 . The method of claim 1 , wherein the agent is the protein or the aptamer.

11 . The method of claim 10 , wherein the agent is an antibody.

12 . The method of claim 11 , wherein the agent is a blocking or neutralizing antibody that binds specifically to BMPR 1A, BMPR 2A, or both BMPR 1A and BMPR 2.

13 . The method of claim 2 , wherein the stem cell is a neural stem cell or a neural progenitor cell.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 10, 2024
From: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
To: CZ BIOHUB SF, LLC; THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 067063/0864 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 6, 2023
From: CHEN, ELIZABETH YANG; REINITZ, FELICIA; ANTONY, JANE; CLARKE, MICHAEL F.; JONES, ROBERT C.
To: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 065783/0312 →