Cardiac Stem Cell Population With CD105 Selection for Low-Inflammation Therapy

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Solution Overview

Problem

Existing cardiac stem cells used for regenerative medicine have limitations in therapeutic efficacy and may cause side effects during transplantation, necessitating the development of improved stem cells with enhanced production abilities and immunoregulatory functions.

Innovation Solution

A cell population comprising human-derived cardiac stem cells with a high proportion of CD105 expression and no αMHC gene, exhibiting enhanced ADM, MMP1, and HGF production abilities, along with specific surface antigen profiles, is developed to improve therapeutic efficacy and minimize side effects.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional cardiac stem cells are used for transplantation, then regenerative treatment for cardiac diseases can be achieved, but therapeutic efficacy is limited and side effects may occur

Engineering Contradiction:
Improvetherapeutic efficacyVSAvoidside effects
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent applies parameter changes by selecting and expanding cardiac stem cells with specific surface antigen expression profiles (CD105≥70%, CD90≥30%, CD45≤10%, CD34≤10%). This parameter-based selection optimizes the cellular composition to enhance therapeutic efficacy while minimizing side effects through controlled differentiation potential and reduced immunogenicity.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent implements local quality by creating a heterogeneous cell population with distinct functional subpopulations. The cell population includes cells with different surface antigen profiles that contribute to various functions: some cells differentiate into cardiomyocytes while others provide paracrine support, creating localized functional zones within the transplant that address multiple therapeutic needs simultaneously.

Inventive Principle:
Principle #3Local quality

2Productivity

If stem cells are selected based on sphere formation in suspension culture, then pluripotent stem cells can be obtained, but production ability and immunoregulatory function are insufficient

Engineering Contradiction:
Improveproduction abilityVSAvoidimmunoregulatory ability
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The patent fundamentally changes the selection parameters from morphology-based (sphere formation) to surface antigen expression-based selection. By using flow cytometry to identify cells with specific antigen profiles (CD105≥70%, CD90≥30%, CD45≤10%, CD34≤10%), the method enriches for cells with enhanced production ability and immunoregulatory function, overcoming the limitations of conventional sphere-based selection.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent replaces the mechanical/morphological selection method (sphere formation in suspension) with a biochemical identification method (surface antigen expression analysis via flow cytometry). This substitution enables more precise selection of cells based on molecular markers that correlate with desired functional properties, thereby improving both productivity and immunoregulatory ability.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

Data Source

PatentEP4671364A1Cell population containing cardiac stem cells
Publication Date: 2025.12.31 METCELA INC
  • EP4671364A1 patent drawingFigure 1
  • EP4671364A1 patent drawingFigure 2A~2H
  • EP4671364A1 patent drawingFigure 3A~3H

AI summary

By expressing specific factors in cardiac stem cells, it was found that their ADM production ability, MMP1 production ability, and/or HGF production ability could be enhanced. Additionally, it was found that such cardiac stem cells exhibit excellent immune-regulatory and/or anti-inflammatory capabilities. Therefore, a cell population comprising such cardiac stem cells can be provided.