Acute myeloid leukemia creates an arginase-dependent immunosuppressive microenvironment

Research output: Contribution to journalArticle

Authors

  • Issa Abu-Dayyeh
  • Lynn Quek
  • Rosanna M McEwen-Smith
  • Amrana Qureshi
  • Francesco Dazzi
  • Paresh Vyas
  • Vincenzo Cerundolo

Colleges, School and Institutes

Abstract

Acute myeloid leukemia (AML) is the most common acute leukemia in adults and the second most common frequent leukemia of childhood. Patients may present with lymphopenia or pancytopenia at diagnosis. We investigated the mechanisms by which AML causes pancytopenia and suppresses patients' immune response. This study identified for the first time that AML blasts alter the immune microenvironment through enhanced arginine metabolism. Arginase II is expressed and released from AML blasts and is present at high concentrations in the plasma of patients with AML, resulting in suppression of T-cell proliferation. We extended these results by demonstrating an arginase-dependent ability of AML blasts to polarize surrounding monocytes into a suppressive M2-like phenotype in vitro and in engrafted nonobese diabetic-severe combined immunodeficiency mice. In addition, AML blasts can suppress the proliferation and differentiation of murine granulocyte-monocyte progenitors and human CD34(+) progenitors. Finally, the study showed that the immunosuppressive activity of AML blasts can be modulated through small-molecule inhibitors of arginase and inducible nitric oxide synthase, suggesting a novel therapeutic target in AML. The results strongly support the hypothesis that AML creates an immunosuppressive microenvironment that contributes to the pancytopenia observed at diagnosis.

Details

Original languageEnglish
Pages (from-to)749-58
Number of pages10
JournalBlood
Volume122
Issue number5
Publication statusPublished - 1 Aug 2013

Keywords

  • Animals, Arginase, Cell Proliferation, Cells, Cultured, Humans, Immune Tolerance, Leukemia, Myeloid, Acute, Mice, Mice, Inbred C57BL, Mice, Inbred NOD, Mice, SCID, Mice, Transgenic, T-Lymphocytes, Transplantation, Heterologous, Tumor Escape, Tumor Microenvironment