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Scientists reprogram so-called MHC molecules, responsible for displaying antigens, to match donor to receipient for Transplantation surgery, using CRISPR/Cas9. After breakthroughs in allogenic iPSC treatment of AMD in Japan, this technique could help prevent GvHD in allogeneic transplantation.
Scientists reprogram so-called MHC molecules, responsible for displaying antigens, to match donor to receipient for Transplantation surgery, using CRISPR/Cas9. After breakthroughs in allogenic iPSC treatment of AMD in Japan, this technique could help prevent GvHD in allogeneic transplantation.
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