Simpore Inc. — Department of Health and Human Services STTR Phase I: NHLBI

Description

Abstract The overall goal of this proposal is to develop systems for efficient ex vivo maturation of functional human red blood cells RBCs which holds tremendous potential for addressing supply bottlenecks for delivering new therapeutic options to chronically transfused patients with severe alloimmunization and for novel strategies for delivering therapeutics via engineered RBCs No approaches developed so far have shown the ability to produce both enucleated and mature RBCs that have reliable shelf life in storage or viability upon transfusion Our hypothesis is that in existing culture systems late stage erythroblasts early reticulocytes lose too much surface area during enucleation and membrane remodeling leading to more spherical cells that are susceptible to hemolysis We propose a biomimetic approach wherein cells are passed through microslit filters to recapitulate in vivo mechanical deformations that appropriately constrain cell area volume promote proper biconcave disc morphology and limit potentially harmful extensional stretching This proposal brings together expertise in microfabrication at SiMPore Inc with RBC biology and rheology at the University of Rochester SiMPore will optimize micro slit manufacturing methods and integrate microslit filter membranes into fluidic systems for RBC maturation testing at Rochester Aim Similar efforts will be carried out to test the capability of microslit filters to separate and concentrate mature enucleated RBCs from nucleated precursors Aim Relevant experts will guide developing regulatory and commercialization plans so that the team is positioned to carry out clinical studies during Phase II The developed RBC maturation tools can be married with existing large volume bioreactors for RBC precursor expansion so that final maturation using this approach can be scaled for practical volumes Narrative A limitation on the blood supply is the inability to grow mature red blood cells RBCs using current culturing methods In this project novel filtration technology will be developed for completing the maturation of cultured RBCs into functionally mature forms and for isolating and concentrating these forms for potential use as a transfusion product