Stem Cell Microparticles for Targeted NK Cell Activation

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Solution Overview

Problem

Existing methods have not effectively utilized exosomes derived from mesenchymal stem cells to control the expression of specific microRNAs for activating NK cells, which are crucial for enhancing their activity, particularly in addressing age-related declines and stress-induced deterioration.

Innovation Solution

Microparticles containing miRNA, specifically hsa-miR-155-5p, derived from the culture supernatant of dental pulp-derived or adipose-derived stem cells, are used to control the expression of proteins and genes related to NK cell activation, promoting the production of granzyme B and regulating SHIP1 expression.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Manufacturing precision

If conventional methods are used to activate NK cells, then general activation occurs, but specific control of miRNA expression and targeted protein regulation is insufficient

Engineering Contradiction:
Improvecontrol precision of miRNA expressionVSAvoidcomplexity of activation system
Core Design Contradiction:
Manufacturing precisionVSDevice complexity

Solution Approach 1:

The patent uses exosomes as intermediary carriers to deliver specific miRNAs (particularly miR-155) to NK cells. These exosomes act as natural delivery vehicles that protect miRNAs from degradation and facilitate their uptake by target cells, enabling precise control of gene expression without complex artificial delivery systems

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent changes the chemical and biological parameters of the activation system by introducing specific miRNAs that target key regulatory proteins (such as SHIP1, PTEN, and SOCS1). This allows precise control of signaling pathways through post-transcriptional regulation, achieving specific activation control without complex multi-component systems

Inventive Principle:
Principle #35Parameter changes

2Reliability

If NK cell activity is enhanced through general stimulation, then overall activation increases, but targeted control of specific activation pathways is limited

Engineering Contradiction:
ImproveNK cell activation effectivenessVSAvoidease of activation method
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The patent extracts and utilizes specific miRNAs (particularly miR-155) from exosomes as the active component for NK cell activation. By isolating and concentrating these specific miRNAs, the method achieves reliable and targeted activation control while simplifying the overall activation approach compared to using complex stimulation mixtures

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

Exosomes serve as natural mediators that deliver specific miRNAs to NK cells, enabling reliable activation through a biologically compatible delivery system. This approach is easier to manufacture than synthetic delivery systems while providing targeted control of activation pathways through specific miRNA-protein interactions

Inventive Principle:
Principle #24Intermediary (Mediator)

3Productivity

If exosomes from mesenchymal stem cells are used to deliver miRNA, then NK cell activation is promoted, but the specific control of miRNA expression and target protein regulation is not fully achieved

Engineering Contradiction:
ImproveNK cell activation efficiencyVSAvoidprecision of gene expression control
Core Design Contradiction:
ProductivityVSManufacturing precision

Solution Approach 1:

The patent applies local quality by introducing specific miRNAs (particularly miR-155) into exosomes at controlled concentrations. This allows different regions or batches of exosomes to have optimized miRNA content tailored for specific activation purposes, achieving both high productivity and precise control of gene expression in NK cells

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The patent optimizes parameters such as miRNA concentration, exosome purification methods, and delivery conditions to achieve both high NK cell activation efficiency and precise control of miRNA expression. By adjusting these parameters, the method simultaneously improves productivity and manufacturing precision

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentUS20260103713A1Microparticle, agent for activating NK cell, method for culturing NK cell, method for producing activated NK cell, and method for activating NK cell
Publication Date: 2026.04.16 DEXON PHARM INC
  • US20260103713A1 patent drawing
  • US20260103713A1 patent drawing

AI summary

Microparticles comprising miRNA with respect to the activation of NK cells and derived from culture supernatant of dental pulp-derived stem cells or culture supernatant of adipose-derived stem cells are new microparticles that enables controlling the expression of proteins and/or genes related to the activation of NK cells; an agent for activating NK cells; a method for culturing NK cells; a method for producing activated NK cells; NK cells; a method for activating NK cells NK cells.