Glutamine protects mice from acute graft-versus-host disease (aGVHD)

Biochem Biophys Res Commun. 2013 May 24;435(1):94-9. doi: 10.1016/j.bbrc.2013.04.047. Epub 2013 Apr 24.

Abstract

Despite current immunosuppressive therapies, acute graft-versus-host disease (aGVHD) is a major cause of morbidity and mortality in allogeneic hematopoietic stem cell transplantation (HSCT). In the present study, therapeutic effects of intraperitoneal glutamine (Gln) administration (1g/kg/day) in a mouse aGVHD model were evaluated. Gln administration significantly inhibited the GVHD-induced inflammation and tissue injury in the intestine, liver, skin and spleen. Gln therapy improved the score of clinical evidence of aGVHD and prolonged the median survival of aGVHD mice. Gln administration in aGVHD mice increased the fraction of Foxp3+/CD4+/CD25+ cells in the blood measured on day 7, and decreased the serum levels of tumor necrosis factor-α measured on days 7, 14 and 21 after aGVHD induction. These results demonstrated that Gln administration may be useful in protecting the host from aGVHD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Animals
  • CD4-Positive T-Lymphocytes / drug effects
  • CD4-Positive T-Lymphocytes / metabolism
  • Cell Transplantation / adverse effects
  • Cell Transplantation / methods*
  • Female
  • Forkhead Transcription Factors / blood
  • Glutamine / administration & dosage
  • Glutamine / pharmacology*
  • Graft vs Host Disease / blood
  • Graft vs Host Disease / etiology
  • Graft vs Host Disease / prevention & control*
  • Inflammation / prevention & control
  • Injections, Intraperitoneal
  • Interferon-gamma / blood
  • Interleukin-2 Receptor alpha Subunit / blood
  • Intestines / drug effects
  • Intestines / pathology
  • Leukocyte Count
  • Liver / drug effects
  • Liver / pathology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Skin / drug effects
  • Skin / pathology
  • Spleen / cytology*
  • Survival Analysis
  • Time Factors
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Il2ra protein, mouse
  • Interleukin-2 Receptor alpha Subunit
  • Tumor Necrosis Factor-alpha
  • Glutamine
  • Interferon-gamma