In this issue of Blood, using genetically deficient donor T cells or posttransplant pharmacologic inhibition, Haarberg et al have conclusively demonstrated that protein kinase C (PKC)-u and PKC-a each contribute to alloreactivity after experimental allogeneic bone marrow transplantation (BMT).
CITATION STYLE
Fowler, D. H. (2013, October 3). Doubling down on PKC benefits allogeneic BMT. Blood. American Society of Hematology. https://doi.org/10.1182/blood-2013-08-519900
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