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Survival of syngeneic and allogeneic iPSC-derived neural precursors after spinal grafting in minipigs
J. Strnadel, C. Carromeu, C. Bardy, M. Navarro, O. Platoshyn, AN. Glud, S. Marsala, J. Kafka, A. Miyanohara, T. Kato, T. Tadokoro, MP. Hefferan, K. Kamizato, T. Yoshizumi, S. Juhas, J. Juhasova, CS. Ho, T. Kheradmand, P. Chen, D. Bohaciakova, M....
Language English Country United States
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
P01 HL066941
NHLBI NIH HHS - United States
R21 MH107771
NIMH NIH HHS - United States
R01 MH094753
NIMH NIH HHS - United States
U19 MH107367
NIMH NIH HHS - United States
R01 OD018272
NIH HHS - United States
- MeSH
- Survival Analysis MeSH
- Cell Differentiation MeSH
- Chronic Disease MeSH
- Fibroblasts cytology MeSH
- Transplantation, Homologous MeSH
- Immunity, Humoral MeSH
- Immune Tolerance MeSH
- Immunosuppression Therapy MeSH
- Induced Pluripotent Stem Cells cytology MeSH
- Rats MeSH
- Skin cytology MeSH
- Spinal Cord transplantation MeSH
- Swine, Miniature MeSH
- Neostriatum pathology MeSH
- Neural Stem Cells cytology transplantation MeSH
- Neurons cytology MeSH
- Spinal Cord Injuries pathology therapy MeSH
- Swine MeSH
- Cellular Reprogramming MeSH
- Gene Expression Regulation MeSH
- Aging MeSH
- Transplantation, Isogeneic MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
The use of autologous (or syngeneic) cells derived from induced pluripotent stem cells (iPSCs) holds great promise for future clinical use in a wide range of diseases and injuries. It is expected that cell replacement therapies using autologous cells would forego the need for immunosuppression, otherwise required in allogeneic transplantations. However, recent studies have shown the unexpected immune rejection of undifferentiated autologous mouse iPSCs after transplantation. Whether similar immunogenic properties are maintained in iPSC-derived lineage-committed cells (such as neural precursors) is relatively unknown. We demonstrate that syngeneic porcine iPSC-derived neural precursor cell (NPC) transplantation to the spinal cord in the absence of immunosuppression is associated with long-term survival and neuronal and glial differentiation. 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 data demonstrate that iPSC-NPCs can be grafted into syngeneic recipients in the absence of immunosuppression and that temporary immunosuppression is sufficient to induce long-term immune tolerance after NPC engraftment into spinally injured allogeneic recipients. Collectively, our results show that iPSC-NPCs represent 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.
Center for iPS Cell Research and Application Kyoto University Kyoto Japan
Columbia University Medical Center Campus New York NY 10032 USA
Department of Neurosurgery UCSD La Jolla CA 92103 USA
Department of Pathology UCSD La Jolla CA 92093 USA
Department of Pediatrics UCSD La Jolla CA 92037 USA
Histocompatibility Laboratory Gift of Life Michigan Ann Arbor MI 48108 USA
Laboratory of Genetics The Salk Institute for Biological Studies La Jolla CA 92037 USA
References provided by Crossref.org
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