PSG1 Tendon Injection to Enhance MSC-Driven Healing

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current treatments for tendon injuries, such as tendonitis and tendinopathy, are inadequate in promoting effective healing and regeneration, particularly in enhancing the migration of mesenchymal stem cells to the injury site.

Innovation Solution

The use of pregnancy-specific glycoproteins (PSG1) and mesenchymal stem cells (MSCs), either co-administered or separately, to enhance tendon healing by promoting MSC migration and regeneration. Administration methods include intra-tendon or peri-tendon injection, topical formulations, and transfection of MSCs with PSG1 expression vectors.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional treatments are used for tendon injuries, then current standard care is provided, but effective healing and regeneration is not promoted

Engineering Contradiction:
Improvehealing effectivenessVSAvoidregeneration rate
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The patent combines PSG1 protein therapy with mesenchymal stem cell (MSC) therapy to treat tendon injuries. The PSG1 protein enhances MSC migration to the injury site and promotes tendon regeneration, creating a synergistic effect that improves healing effectiveness beyond what either treatment achieves alone.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

PSG1 acts as a mediator protein that facilitates the interaction between MSCs and the tendon injury site. It enhances MSC migration, survival, and differentiation into tendon-specific cells, thereby promoting effective healing and regeneration.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If PSG1 and MSCs are co-administered, then tendon healing is enhanced, but treatment complexity increases

Engineering Contradiction:
Improvehealing enhancementVSAvoidtreatment protocol
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The treatment can be segmented into separate administration of PSG1 protein and MSCs, or combined administration depending on clinical needs. The PSG1 protein can be administered alone as a preliminary treatment to prepare the injury site, followed by MSC injection, or both can be administered together in a single procedure.

Inventive Principle:
Principle #1Segmentation

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

Enhances tendon healing by improving MSC migration to the injury site, potentially halting, slowing, or reversing tendon degeneration, and providing symptomatic relief for tendon pain and stiffness.

Implementation Method 1

The Applicant has discovered that a pregnancy-specific glycoprotein (for example PSG1) enhances the migration of mesenchymal stem cells (MSCs).

Methodology Applied
Scientific EffectCell migration:

Implementation Method 2

PSG1 is involved in activation of transforming growth factor-β 1 (TGFß1), a cytokine essential to suppression of inflammatory T-cells

Methodology Applied
Scientific EffectCytokine activation:

Implementation Method 3

important for differentiation of tolerance inducing CD4+CD25+FoxP3+ regulatory T cells (Tregs), a cell population shown to be important in the prevention of Graft versus Host Disease (GvHD)

Methodology Applied
Scientific EffectCell differentiation:

Data Source

PatentUS20260022147A1Placenta expressed proteins for use in the treatment of tendon injury
Publication Date: 2026.01.22 UNIV COLLEGE CORK NAT UNIV OF IRELAND CORK
  • US20260022147A1 patent drawing

AI summary

The use of Fc-tagged Pregnancy-specific glycoprotein 1 (PSG1-Fc) in a method of treatment of a tendon injury in a human, in which the PSG1 is administered by intra-tendon or peri-tendon injection, is described. Also described is the use of CC49 in a method of treatment of tendonitis, tendinosis, tendinopathy, or tendon damage in an equine mammal, in which the CC49 is administered by intra-tendon or peri-tendon injection.