Hyperglycemia and increased insulin requirements are indicators of ongoing islet allograft rejection, but there are no methods to predict or confirm rejection. Elevation of cytotoxic lymphocyte (CL) gene expression in peripheral blood (PB) has been correlated with renal allograft rejection in humans, but no published study has assessed the utility of monitoring these markers as predictors of rejection before the onset of clinical symptoms. We have established quantitative real-time PCR methods to determine the levels of mRNA transcripts for the CL genes granzyme B (GB), perforin, and fas ligand in blood samples from rhesus and cynomolgus monkeys. Four rhesus monkeys with long-term islet allograft function were studied. Antirejection (anti-CD154) therapy was discontinued, and weekly PB samples were obtained to determine whether the levels of mRNA transcripts for CL genes correlated with and/or were predictive of islet allograft rejection, defined as a loss of C-peptide production. For all monkeys, elevation of CL gene expression preceded rejection by 83--197 days, with GB as the best predictor. Elevated mRNA levels were sustained for 2--2.5 months in three of four animals and 1 month in the other, thus suggesting that the testing of these parameters may have practical applications in clinical islet cell transplantation.

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http://dx.doi.org/10.2337/diabetes.51.3.562DOI Listing

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Article Synopsis
  • - The research focuses on developing small-molecule inhibitors (SMIs) targeting the CD40-CD40L interaction to improve islet transplantation outcomes and prevent type 1 diabetes (T1D) in mice.
  • - Promising SMIs DRI-C21041 and DRI-C21095 demonstrated the ability to prolong islet allograft survival and functionality while reducing T1D incidence in NOD mice during trials.
  • - These findings suggest that CD40L-targeting SMIs could provide a safer and more effective alternative to traditional antibody treatments, offering better control and ease of administration for transplant recipients and autoimmune disease prevention.
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As an effective treatment for diabetes, islet transplantation has garnered significant attention and research in recent years. However, immune rejection and the toxicity of immunosuppressive drugs remain critical factors influencing the success of islet transplantation. While immunosuppressants are essential in reducing immune rejection reactions and can significantly improve the survival rate of islet transplants, improper use of these drugs can markedly increase mortality rates following transplantation.

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