Bioengineered Allogeneic Blood Vessel via Decellularization and Recellularization
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Solution Overview
Problem
Current sources for vascular grafts, such as allogeneic, animal, and artificial blood vessels, face issues like scarcity, poor patency, transplant rejection, and immunosuppression complications, necessitating a more effective and safer method for producing allogeneic blood vessels.
Innovation Solution
A method involving decellularization of blood vessels followed by recellularization using autologous cells, where cells from the patient are introduced to a decellularized blood vessel and cultured to differentiate into functional endothelial and smooth muscle cells, creating a bioengineered vessel suitable for implantation.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Quantity of substance
If allogeneic blood vessels are used for vascular grafts, then graft availability is improved, but transplant rejection and immunosuppression complications occur
Solution Approach 1:
The patent extracts and removes cellular components (nuclei, cell membranes) from donor blood vessels through decellularization processes, retaining only the extracellular matrix scaffold. This eliminates donor-specific antigens that cause rejection while preserving the vessel structure for implantation.
Solution Approach 2:
The patent fundamentally changes the biological state of the graft by transitioning from a cellular-containing state to a decellularized state, then recellularizing with recipient-derived cells. This parameter change eliminates immunogenicity while maintaining structural integrity.
2Quantity of substance
If decellularization is performed on blood vessels, then graft availability and non-immunogenicity are improved, but manufacturing complexity increases
Solution Approach 1:
The patent performs decellularization as a preliminary processing step on donor vessels before implantation. By pre-processing the vessels in this manner, the complex multi-step process is consolidated into a preparatory phase, simplifying the overall manufacturing workflow.
3Reliability
If autologous cells are used for recellularization, then graft compatibility is improved, but cell source availability and processing time are worsened
Solution Approach 1:
The patent employs the recipient's own cells (autologous cells) to recellularize the decellularized vessel scaffold. The cells are derived from the recipient's bone marrow or peripheral blood, ensuring perfect compatibility and eliminating rejection risks while using the patient's self-resources.
4Loss of time
If conventional blood vessel sources are used, then immediate availability is improved, but long-term patency and durability are worsened
Solution Approach 1:
The patent creates a composite structure combining the decellularized donor vessel scaffold (providing immediate structural availability) with autologous recipient cells (providing long-term durability and patency). This composite approach merges the advantages of both immediate availability and long-term survival.
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
This approach provides a non-immunogenic, longer-lasting, and more readily available vascular graft with preserved angiogenic growth factors and biomechanical integrity, reducing the need for immunosuppression and minimizing graft rejection risks.
Implementation Method 1
preserved angiogenic growth factors
Implementation Method 2
cells from the patient are introduced to a decellularized blood vessel and cultured to differentiate into functional endothelial and smooth muscle cells
Data Source
AI summary
The present invention relates to methods for recellurization of blood vessels. This method is particularly useful for producing an allogeneic vein, wherein a donor vein is decellularized and then recellularized using whole blood or bone marrow stem cells. The allogeneic veins produced by the methods disclosed herein are particularly advantageous for implantation or transplantation into patients with vascular diseases.


