Imagine a world in which it is possible to replace dead cardiomyocytes after a heart attack, missing dopaminergic neurons in patients with Parkinson’s Disease, or hepatocytes in patients with damaged livers.
Differentiating stem cells into clinically needed cell types has the potential to transform the way we treat a host of diseases. Cell replacement therapy offers the opportunity to turn this vision into a reality.
The key challenges in the field are making the appropriate cells at scale and then having them engraft, function, and persist. Making impactful medicines in this field requires success in all of these components.
Engraft = developing the right delivery system, understanding the underlying microenvironment, and ensuring cells have the right features to succeed
Function = understand and reproducibly manufacture the exact cell needed
Persist = overcome immune rejection and cell death
We view the most challenging barrier to be overcoming immune rejection from transplanting a ‘non-self’ cell. Sana has assembled a team of leaders in this area, and successful development of this capability will make cellular therapy products widely accessible.Next