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- URN to cite this document:
- urn:nbn:de:bvb:355-epub-583453
- DOI to cite this document:
- 10.5283/epub.58345
Abstract
The adoptive transfer of regulatory T cells is a promising strategy to prevent graft-versus-host disease after allogeneic bone marrow transplantation. Here, we use a major histocompatibility complex-mismatched mouse model to follow the fate of in vitro expanded donor regulatory T cells upon migration to target organs. Employing comprehensive gene expression and repertoire profiling, we show that ...

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