C3

C3: Treatment of type 1 diabetes with porcine islet cells: transplantation of multi-transgenic islets expressing immunomodulatory molecules

The aim of the project is to cure type 1 diabetes by transplantation (Tx) of transgenic porcine beta cells. In previous studies we provide the proof-of-principle that overexpression of the immunomodulatory molecule LEA29Y in porcine islets prevents T cell-meditated xenorejection in humanized NOD-scid-IL2 receptor gammanull (NSG) mice. Since protection from rejection was not observed in animals carrying a fully matured immune system, it is planned to knockout major porcine xenoantigens, to overexpress multiple transgenes targeting T cells, B cells and innate immune cells and to study their effects in several mouse models with and without addition of low-dose immunosuppressive drugs. When rejection of transplanted beta cells is inhibited, efficiency of the method will be confirmed by Tx in non-human primates to provide the preclinical studies for the transfer of this novel approach to the clinic.

 Immunhistologische Färbung von isolierten neonatalen porcinen Inselzellclustern: Färbung mit Cytokeratin-Antikörper (rot) und Insulin (Grün)
 Immunhistologie einer transplantierten  INSLEA29Y transgenen Langerhans´schen Insel. Insulin (rot), Glukagon (braun)
 Hemmung der Abstoßungsreaktion durch Expression von LEA29Y in porzinen Inselzellen. LEA29Ytg Inseln sind nach Transplantation in diabetische  NSG Mäuse, die ein humanes Immunsystem tragen, über 6  Monate vor der Abstoßung geschützt ohne zusätzliche Gabe von Immunsuppressiva. Färbung mit Insulinantikörper (rot) und Antikörper gegen CD45 auf humanen Leukozyten (braun)