Neural Cells Repair Spinal Cord Damage without Triggering Rejection

No tumor formation was noted. Similar cell engraftment and differentiation were shown in spinally injured transiently immunosuppressed swine leukocyte antigen (SLA)–mismatched allogeneic pigs.

These findings demonstrated that iPSC-NPCs could be grafted into syngeneic recipients in the absence of immunosuppression and that temporary immunosuppression was sufficient to induce long-term immune tolerance after NPC engraftment into spinally injured allogeneic recipients. Thus, it was shown that iPSC-NPCs represented an alternative source of transplantable NPCs for the treatment of a variety of disorders affecting the spinal cord, including trauma, ischemia, or amyotrophic lateral sclerosis.

“The promise of iPSCs is huge, but so too have been the challenges. In this study, we have demonstrated an alternate approach,” said senior author Dr. Martin Marsala, professor of anesthesiology at the University of California, San Diego. “We took skin cells from an adult pig, an animal species with strong similarities to humans in spinal cord and central nervous system anatomy and function, reprogrammed them back to stem cells, then induced them to become neural precursor cells (NPCs), destined to become nerve cells. Because they are syngeneic - genetically identical with the cell-graft recipient pig - they are immunologically compatible. They grow and differentiate with no immunosuppression required.”

“Our current experiments are focusing on generation and testing of clinical grade human iPSCs, which is the ultimate source of cells to be used in future clinical trials for treatment of spinal cord and central nervous system injuries in a syngeneic or allogeneic setting,” said Dr. Marsala. “Because long-term post-grafting periods - one to two years - are required to achieve a full grafted cells-induced treatment effect, the elimination of immunosuppressive treatment will substantially increase our chances in achieving more robust functional improvement in spinal trauma patients receiving iPSC-derived NPCs.”

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University of California, San Diego