The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jun. 29, 2021

Filed:

Jun. 16, 2017
Applicant:

Dongguk University Industry-academic Cooperation Foundation, Seoul, KR;

Inventors:

Gun Il Im, Anyang-si, KR;

Jong Min Lee, Goyang-si, KR;

Ji Yun Ko, Goyang-si, KR;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 35/28 (2015.01); C07K 14/47 (2006.01); C12N 15/85 (2006.01); A61K 48/00 (2006.01); A61K 35/00 (2006.01); A61K 38/00 (2006.01); C12N 15/90 (2006.01);
U.S. Cl.
CPC ...
A61K 35/28 (2013.01); A61K 48/0066 (2013.01); C07K 14/47 (2013.01); C12N 15/85 (2013.01); A61K 35/00 (2013.01); A61K 38/00 (2013.01); C12N 15/907 (2013.01); C12N 2840/20 (2013.01); C12Y 301/22001 (2013.01); Y02A 50/30 (2018.01);
Abstract

The present invention relates to a non-viral minicircle vector expressing a SOX gene, a stem cell into which the vector is introduced, a pharmaceutical composition for preventing or treating a cartilage disease, including the stem cell, and a method for constructing the vector. The transformation of mesenchymal stem cells with MC/SOX-Trio or MC/SOX-Duo, which is a non-viral minicircle vector according to the present invention, can completely exclude the necessity of expensive growth factors that have been indispensably used in inducing the differentiation of mesenchymal stem cells into chondrocytes. Accordingly, the mesenchymal stem cells transformed therewith, when implanted in vivo, can differentiate into chondrocytes by themselves, and thus have an advantage capable of simplifying the existing complicated steps of culturing cells to induce differentiation and then transplanting the cells. Further, unlike existing vector systems in which antibiotic-resistant genes and other bacteria-derived exogenous genes are simultaneously transferred to cells even after transformation, the vector of the present invention minimizes transfer of unnecessary genes into target cells by allowing two or three SOX genes necessary only for differentiation into chondrocytes to be regulated under one promoter, and thus can be utilized as a non-viral vector system in the most advantageous form for use in clinical application of stem cell-gene therapeutic agents.


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