Specific immunosuppressive role of nanodrugs targeting calcineurin in innate myeloid cells

Calcineurin (CN) inhibitors currently used to avoid transplant rejection block the activation of adaptive immune responses but also prevent the development of tolerance toward the graft, by directly inhibiting T cells. CN, through the transcription factors of the NFAT family, plays an important role also in the differentiation dendritic cells (DCs), the main cells responsible for the activation of T lymphocytes. Therefore, we hypothesized that the inhibition of CN only in DCs and not in T cells could be sufficient to prevent T cell responses, while allowing for the development of tolerance. Here, we show that inhibition of CN/NFAT pathway in innate myeloid cells, using a new nanoconjugate capable of selectively targeting phagocytes in vivo, protects against graft rejection and induces a longer graft acceptance compared to common CN inhibitors. We propose a new generation of nanoparticles-based selective immune suppressive agents for a better control of transplant acceptance.

Automated summary

Calcineurin inhibitors can prevent transplant rejection but also hinder graft tolerance. Inhibiting calcineurin only in dendritic cells instead of T cells can prevent T cell responses while allowing for tolerance development. A new generation of selective immune suppressive agents based on nanoparticles shows promise for better control of transplant acceptance.