Red blood cell arginase suppresses Jurkat (T cell) proliferation by depleting arginine

Andrew Bernard, Michael Kasten, Cindy Meier, Erin Manning, Stephanie Freeman, Will Adams, Phillip Chang, Bernard Boulanger, Paul Kearney

Research output: Contribution to journalArticlepeer-review

18 Scopus citations


Background: Transfusion of packed red blood cells (PRBC) suppresses immunity, but the mechanisms are incompletely understood. PRBCs contain arginase, an enzyme which converts arginine to ornithine and depletes arginine in vitro. Arginine depletion suppresses proliferation of Jurkat T cells in other models. We hypothesize that PRBC arginase-mediated arginine depletion will suppress proliferation of T cells. Methods: A transfusion model was designed adding PRBC to culture RPMI media with or without an irreversible arginase blocker (nor-NOHA), incubating for 6-48 hours and then removing the PRBCs. Amino acid concentrations in the media were measured using liquid chromatography mass spectrometry. T cells were then added to the pre-conditioned media, cultured for 24 hours, and proliferation was measured. Results: PRBC depleted arginine significantly and increased ornithine in media compared to baseline PRBC treated wells and significantly decreased T cell proliferation. These effects were enhanced with volume of PRBC exposure. Nor-NOHA inhibition of arginase restored T cell proliferation in PRBC treated cultures. Conclusions: Jurkat T cell proliferation was impaired by PRBC in clinically relevant volumes. The mechanism influencing T cell impairment appears to result from arginine depletion by arginase. Arginine depletion by PRBC arginase may be a novel mechanism for immunosuppression after transfusion.

Original languageEnglish
Pages (from-to)286-291
Number of pages6
Issue number2
StatePublished - Feb 2008

ASJC Scopus subject areas

  • Surgery


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