Method for treatment of GM1 gangliosidosis

Patent metadata

Field	Value
Publication number	US-10035830-B2
Application number	US-201514820348-A
Country	US
Kind code	B2
Filing date	Aug 6, 2015
Priority date	Sep 5, 2014
Publication date	Jul 31, 2018
Grant date	Jul 31, 2018

Abstract

The present invention relates to a method for preparing a GM1 gangliosidosis human cell model based on induced pluripotent stem cells (iPSCs) and iPSCs originated neural progenitor cells, and a use of the GM1 model above for the development of a GM1 gangliosidosis treating agent. The iPSCs originated from GM1 patient fibroblasts can be differentiated into neural progenitor cells (NPCs) and neurosphere cells that can emulate the characteristics shown in GM1 patient, so that the said cells can be efficiently used for the investigation of intracellular GM1 symptoms such as the GM1 gangliosidosis and lysosome accumulation and the gene expression pattern change. So, the GM1 cell model of the present invention can be efficiently used for the study of GM1 development mechanism and the study for the development of a therapeutic agent for the disease. The present inventors also established the inflammasome inhibitor rhIL1RA or Z-YVAD-FMK by using the above GM1 cell model and further confirmed that it can be efficiently used as a relieving/treating agent of GM1 gangliosidosis.

First claim

What is claimed is:

1. A method for treatment of GM1 gangliosidosis comprising:
selecting a subject with GM1 gangliosidosis; and
administering a pharmaceutically effective dose of Z-YVAD-FMK (methyl (3S)-3-[(2S)-2-[(2S)-2-(2-{[(benzyloxy)carbonyl]amino}-3-(4-hydroxyphenyl)propanamido)-3-methylbutanamido]propanamido]-5-fluoro-4-oxopentanoate) to the subject, thereby treating the GM1 gangliosidosis.

2. The method for treatment of GM1 gangliosidosis according to claim 1 , wherein the Z-YVAD-FMK recovers GM1 patient-specific neuronal progenitor cell morphology to a normal shape.

3. A method for altering expression of neuronal genes in neuronal cells in a subject with GM1 gangliosidosis, comprising:
selecting a subject with GM1 gangliosidosis; and
administering a pharmaceutically effective dose of Z-YVAD-FMK (methyl (3S)-3-[(2S)-2-[(2S)-2-(2-{[(benzyloxy)car bonyl]amino}-3-(4-hydroxyphenyl)propanamido)-3-methylbutanamido]propanamido]-5-fluoro-4-oxopentanoate) to the subject, thereby altering the expression of neuronal marker genes in neuronal cells in the subject with GM1 gangliosidosis.

4. The method of claim 3 , wherein the neuronal genes comprise a gene encoding GLB1 and a gene encoding B4GALNT.

5. The method of claim 4 , wherein expression of the gene encoding GLB1 is reduced and expression of the gene encoding B4GALNT is increased by the pharmaceutically effective dose of Z-YVAD-FMK (methyl (3S)-3-[(2S)-2-[(2S)-2-(2-{[(benzyloxy)car bonyl]amino}-3-(4-hydroxyphenyl)propanamido)-3-methylbutanamido]propanamido]-5-fluoro-4-oxopentanoate).

6. The method of claim 1 , wherein treating the GM1 gangliosidosis comprises altering expression of neuronal genes in neuronal cells in the subject.

Assignees

• Korea Res Inst Bioscience & Biotechnology

Inventors

• Cho Yee Sook
• Son Mi Young
• Kwak Jae Eun
• Seol Binna
• Jeon Hye Jin

Classifications

• C12N2510/00

  Genetically modified cells · CPC title

• C12N2506/45

  from artificially induced pluripotent stem cells · CPC title

• C12N2506/1307

  from adult fibroblasts · CPC title

• C12N2501/999

  Small molecules not provided for elsewhere · CPC title

• C12N2501/70

  Enzymes · CPC title