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Rogers, S.A., Chen, F., Talcott, M., Liapis, H. and Hammerman M.R. (2006) Glucose tolerance normalization following transplantation of pig pancreatic primordia into non-immunosuppressed diabetic ZDF rats. Transplant Immunology, 16, 176-184. doi:10.1016/j.trim.2006.08.007

has been cited by the following article:

• TITLE: Xenotransplantation of embryonic pig pancreas for treatment of diabetes mellitus in non-human primates

  AUTHORS: Marc R. Hammerman

  KEYWORDS: Beta Cell; Diabetes Mellitus; Non-Human Primates; Transplantation; Xenotransplantation

  JOURNAL NAME: Journal of Biomedical Science and Engineering, Vol.6 No.5A, May 22, 2013

  ABSTRACT: Transplantation therapy for diabetes in humans is limited by the low availability of human donor whole pancreas or islets. Outcomes are complicated by immunosuppressive drug toxicity. Xenotransplantation is a strategy to overcome supply problems. Implantation of tissue obtained early during embryogenesis is a way to reduce transplant immunogenicity. Pig insulin is biologically active in humans. In that regard the pig is an appropriate xenogeneic organ donor. Insulin-producing cells originating from embryonic pig pancreas obtained very early following pancreatic primordium formation [embryonic day 28 (E28)] engraft long-term in rhesus macaques. Endocrine cells originating from embryonic pig pancreas transplanted in host mesentery migrate to mesenteric lymph nodes, engraft, differentiate and improve glucose tolerance in rhesus macaques without the need for immune suppression. Transplantation of embryonic pig pancreas is a novel approach towards beta cell replacement therapy that could be applicable to humans.